97 results on '"Goto-Inoue N"'
Search Results
2. Dominant-negative effects of a novel mutation in the filamin myopathy.
- Author
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Kono S, Nishio T, Takahashi Y, Goto-Inoue N, Kinoshita M, Zaima N, Suzuki H, Fukutoku-Otsuji A, Setou M, Miyajima H, Kono, S, Nishio, T, Takahashi, Y, Goto-Inoue, N, Kinoshita, M, Zaima, N, Suzuki, H, Fukutoku-Otsuji, A, Setou, M, and Miyajima, H
- Published
- 2010
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3. Imaging mass spectrometry revealed the production of lyso-phosphatidylcholine in the injured ischemic rat brain
- Author
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Koizumi, S., primary, Yamamoto, S., additional, Hayasaka, T., additional, Konishi, Y., additional, Yamaguchi-Okada, M., additional, Goto-Inoue, N., additional, Sugiura, Y., additional, Setou, M., additional, and Namba, H., additional
- Published
- 2010
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4. The specific localization of seminolipid molecular species on mouse testis during testicular maturation revealed by imaging mass spectrometry
- Author
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Goto-Inoue, N., primary, Hayasaka, T., additional, Zaima, N., additional, and Setou, M., additional
- Published
- 2009
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5. Assessing Molecular Localization of Symbiont Microalgae in Coral Branches Through Mass Spectrometry Imaging.
- Author
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Sasaki S, Mori T, Enomoto H, Nakamura S, Yokota H, Yamashita H, and Goto-Inoue N
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- Animals, Coral Reefs, Molecular Imaging methods, Anthozoa metabolism, Symbiosis, Dinoflagellida, Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization methods, Microalgae metabolism
- Abstract
Reef-building corals are a fundamental pillar of coral reef ecosystems in tropical and subtropical shallow environments. Corals harbor symbiotic dinoflagellates belonging to the family Symbiodiniaceae, commonly known as zooxanthellae. Extensive research has been conducted on this symbiotic relationship, yet the fundamental information about the distribution and localization of Symbiodiniaceae cells in corals is still limited. This information is crucial to understanding the mechanism underlying the metabolite exchange between corals and their algal symbionts, as well as the metabolic flow within holobionts. To examine the distribution of Symbiodiniaceae cells within corals, in this study, we used fluorescence imaging and matrix-assisted laser desorption/ionization (MALDI) mass spectrometry imaging (MS-Imaging) on branches of the Acropora tenuis coral. We successfully prepared frozen sections of the coral for molecular imaging without fixing or decalcifying the coral branches. By combining the results of MS-Imaging with that of the fluorescence imaging, we determined that the algal Symbiodiniaceae symbionts were not only localized in the tentacle and surface region of the coral branches but also inhabited the in inner parts. Therefore, the molecular imaging technique used in this study could be valuable to further investigate the molecular dynamics between corals and their symbionts., (© 2024. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.)
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- 2024
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6. A lipidomics approach reveals novel phospholipid changes in palmitate-treated C2C12 myotubes.
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Tawara W, Morisasa M, Mukai R, Suo R, Itoi S, Mori T, and Goto-Inoue N
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- Humans, Palmitates pharmacology, Phospholipids metabolism, Lipidomics, Signal Transduction, Muscle Fibers, Skeletal metabolism, Muscle, Skeletal metabolism, Ceramides metabolism, Diabetes Mellitus, Type 2 drug therapy, Diabetes Mellitus, Type 2 metabolism, Insulin Resistance physiology
- Abstract
Type 2 diabetes mellitus (T2DM) is a highly prevalent metabolic disorder. Insulin resistance and oxidative stress are associated with T2DM development. The hypothesis that patients with T2DM show excess accumulation of lipids, such as ceramides (Cers) and diacylglycerols (DAGs), in their skeletal muscles has been widely supported; however, detailed lipidomic data at the molecular species level are limited. Therefore, in this study, we aimed to investigate the in vitro dynamics of total lipids, including phospholipids (PLs), sphingolipids, and neutral lipids, in palmitic acid-induced insulin-resistant C2C12 skeletal muscle cells. Our data demonstrated that the profiles of not only Cers and DAGs but also those of PLs showed considerably differences after palmitate treatment. We found that PL synthesis reduced and PL degradation increased after palmitate treatment. These findings may aid in the development of treatments to ameliorate muscle dysfunction caused by lipid accumulation in muscles., (© 2024 AOCS.)
- Published
- 2024
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7. LPGAT1/LPLAT7 regulates acyl chain profiles at the sn-1 position of phospholipids in murine skeletal muscles.
- Author
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Sato T, Umebayashi S, Senoo N, Akahori T, Ichida H, Miyoshi N, Yoshida T, Sugiura Y, Goto-Inoue N, Kawana H, Shindou H, Baba T, Maemoto Y, Kamei Y, Shimizu T, Aoki J, and Miura S
- Subjects
- Animals, Mice, Muscle Fibers, Slow-Twitch metabolism, Phosphatidylcholines metabolism, Stearates metabolism, Plasmalogens, Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha metabolism, Muscle Fibers, Skeletal metabolism, Muscle Fibers, Fast-Twitch metabolism, Muscle, Skeletal metabolism, Phospholipids chemistry, Phospholipids genetics, Phospholipids metabolism
- Abstract
Skeletal muscle consists of both fast- and slow-twitch fibers. Phospholipids are important structural components of cellular membranes, and the diversity of their fatty acid composition affects membrane characteristics. Although some studies have shown that acyl chain species in phospholipids differ among various muscle fiber types, the mechanisms underlying these differences are unclear. To investigate this, we analyzed phosphatidylcholine (PC) and phosphatidylethanolamine (PE) molecules in the murine extensor digitorum longus (EDL; fast-twitch) and soleus (slow-twitch) muscles. In the EDL muscle, the vast majority (93.6%) of PC molecules was palmitate-containing PC (16:0-PC), whereas in the soleus muscle, in addition to 16:0-PC, 27.9% of PC molecules was stearate-containing PC (18:0-PC). Most palmitate and stearate were bound at the sn-1 position of 16:0- and 18:0-PC, respectively, and 18:0-PC was found in type I and IIa fibers. The amount of 18:0-PE was higher in the soleus than in the EDL muscle. Peroxisome proliferator-activated receptor γ coactivator-1α (PGC-1α) increased the amount of 18:0-PC in the EDL. Lysophosphatidylglycerol acyltransferase 1 (LPGAT1) was highly expressed in the soleus compared with that in the EDL muscle and was upregulated by PGC-1α. LPGAT1 knockout decreased the incorporation of stearate into PC and PE in vitro and ex vivo and the amount of 18:0-PC and 18:0-PE in murine skeletal muscle with an increase in the level of 16:0-PC and 16:0-PE. Moreover, knocking out LPGAT1 decreased the amount of stearate-containing phosphatidylserine (18:0-PS), suggesting that LPGAT1 regulated the acyl chain profiles of phospholipids, namely, PC, PE, and PS, in the skeletal muscle., Competing Interests: Conflict of interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 The Authors. Published by Elsevier Inc. All rights reserved.)
- Published
- 2023
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8. Smart utilization of betaine lipids in the giant clam Tridacna crocea .
- Author
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Sakai R, Goto-Inoue N, Yamashita H, Aimoto N, Kitai Y, and Maruyama T
- Abstract
The giant clam Tridacna crocea thrives in poorly nourished coral reef water by forming a holobiont with zooxanthellae and utilizing photosynthetic products of the symbiont. However, detailed metabolic crosstalk between clams and symbionts is elusive. Here, we discovered that the nonphosphorous microalgal betaine lipid DGCC (diacylglycerylcarboxy-hydroxymethylcholine) and its deacylated derivative GCC are present in all tissues and organs, including algae-free sperm and eggs, and are metabolized. Colocalization of DGCC and PC (phosphatidylcholine) evidenced by MS imaging suggested that DGCC functions as a PC substitute. The high content of GCC in digestive diverticula (DD) suggests that the algal DGCC was digested in DD for further utilization. Lipidomics analysis showing the organ-specific distribution pattern of DGCC species suggests active utilization of DGCC as membrane lipids in the clam. Thus, the utilization of zooxanthellal DGCC in animal cells is a unique evolutionary outcome in phosphorous-deficient coral reef waters., Competing Interests: The authors declare no competing interests., (© 2023 The Authors.)
- Published
- 2023
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9. Novel predator-induced phenotypic plasticity by hemoglobin and physiological changes in the brain of Xenopus tropicalis .
- Author
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Mori T, Machida K, Kudou Y, Kimishima M, Sassa K, Goto-Inoue N, Minei R, Ogura A, Kobayashi Y, Kamiya K, Nakaya D, Yamamoto N, Kashiwagi A, and Kashiwagi K
- Abstract
Organisms adapt to changes in their environment to survive. The emergence of predators is an example of environmental change, and organisms try to change their external phenotypic systems and physiological mechanisms to adapt to such changes. In general, prey exhibit different phenotypes to predators owing to historically long-term prey-predator interactions. However, when presented with a novel predator, the extent and rate of phenotypic plasticity in prey are largely unknown. Therefore, exploring the physiological adaptive response of organisms to novel predators is a crucial topic in physiology and evolutionary biology. Counterintuitively, Xenopus tropicalis tadpoles do not exhibit distinct external phenotypes when exposed to new predation threats. Accordingly, we examined the brains of X. tropicalis tadpoles to understand their response to novel predation pressure in the absence of apparent external morphological adaptations. Principal component analysis of fifteen external morphological parameters showed that each external morphological site varied nonlinearly with predator exposure time. However, the overall percentage change in principal components during the predation threat (24 h) was shown to significantly ( p < 0.05) alter tadpole morphology compared with that during control or 5-day out treatment (5 days of exposure to predation followed by 5 days of no exposure). However, the adaptive strategy of the altered sites was unknown because the changes were not specific to a particular site but were rather nonlinear in various sites. Therefore, RNA-seq, metabolomic, Ingenuity Pathway Analysis, and Kyoto Encyclopedia of Genes and Genomes analyses were performed on the entire brain to investigate physiological changes in the brain, finding that glycolysis-driven ATP production was enhanced and ß -oxidation and the tricarboxylic acid cycle were downregulated in response to predation stress. Superoxide dismutase was upregulated after 6 h of exposure to new predation pressure, and radical production was reduced. Hemoglobin was also increased in the brain, forming oxyhemoglobin, which is known to scavenge hydroxyl radicals in the midbrain and hindbrain. These suggest that X. tropicalis tadpoles do not develop external morphological adaptations that are positively correlated with predation pressure, such as tail elongation, in response to novel predators; however, they improve their brain functionality when exposed to a novel predator., Competing Interests: Authors YKo, KnK, and DN were employed by the company Milk. Inc. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest., (Copyright © 2023 Mori, Machida, Kudou, Kimishima, Sassa, Goto-Inoue, Minei, Ogura, Kobayashi, Kamiya, Nakaya, Yamamoto, Kashiwagi and Kashiwagi.)
- Published
- 2023
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10. Stable isotope-labeled carnitine reveals its rapid transport into muscle cells and acetylation during contraction.
- Author
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Furuichi Y, Goto-Inoue N, Uchida S, Masuda S, Manabe Y, and Fujii NL
- Abstract
Carnitine plays multiple roles in skeletal muscle metabolism, including fatty acid transport and buffering of excess acetyl-CoA in the mitochondria. The skeletal muscle cannot synthesize carnitine; therefore, carnitine must be taken up from the blood into the cytoplasm. Carnitine metabolism, its uptake into cells, and the subsequent reactions of carnitine are accelerated by muscle contraction. Isotope tracing enables the marking of target molecules and monitoring of tissue distribution. In this study, stable isotope-labeled carnitine tracing was combined with matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) imaging to determine carnitine distribution in mouse skeletal muscle tissues. Deuterium-labeled carnitine (d3-carnitine) was intravenously injected into the mice and diffused to the skeletal muscles for 30 and 60 min. To examine whether muscle contraction changes the distribution of carnitine and its derivatives, unilateral in situ muscle contraction was performed; 60 min muscle contraction showed increased d3-carnitine and its derivative d3-acetylcarnitine in the muscle, indicating that carnitine uptake in cells is promptly converted to acetylcarnitine, consequently, buffering accumulated acetyl-CoA. While the endogenous carnitine was localized in the slow type fibers rather than fast type, the contraction-induced distributions of d3-carnitine and acetylcarnitine were not necessarily associated with muscle fiber type. In conclusion, the combination of isotope tracing and MALDI-MS imaging can reveal carnitine flux during muscle contraction and show the significance of carnitine in skeletal muscles., Competing Interests: The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (© 2023 The Authors.)
- Published
- 2023
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11. Changes in Tissue Distribution of Tetrodotoxin and Its Analogues in Association with Maturation in the Toxic Flatworm, Planocera multitentaculata.
- Author
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Oyama H, Ito M, Suo R, Goto-Inoue N, Morisasa M, Mori T, Sugita H, Mori T, Nakahigashi R, Adachi M, Nishikawa T, and Itoi S
- Subjects
- Animals, Male, Tetrodotoxin, Chromatography, Liquid methods, Tissue Distribution, Tandem Mass Spectrometry methods, Semen metabolism, Larva metabolism, Platyhelminths
- Abstract
The toxic flatworm, Planocera multitentaculata, possesses highly concentrated tetrodotoxin (TTX), also known as pufferfish toxin, throughout its life cycle, including the egg and larval stages. Additionally, TTX analogues, 5,6,11-trideoxyTTX and 11-norTTX-6(S)-ol, have also been detected in the flatworm. The high concentration of TTX in the eggs and larvae appears to be for protection against predation, and 11-norTTX-6(S)-ol in the pharyngeal tissue in the adults is likely used to sedate or kill prey during predation. However, information on the role of 5,6,11-trideoxyTTX, a potential important biosynthetic intermediate of TTX, in the toxic flatworm is lacking. Here, we aimed to determine the region of localization of TTX and its analogues in the flatworm body, understand their pharmacokinetics during maturation, and speculate on their function. Flatworm specimens in four stages of maturity, namely juvenile, mating, spawning, and late spawning, were subjected to LC-MS/MS analysis, using the pharyngeal tissue, oocytes in seminal receptacle, sperm, and tissue from 12 other sites. Although TTX was consistently high in the pharyngeal tissue throughout maturation, it was extremely high in the oocytes during the spawning period. Meanwhile, 5,6,11-trideoxyTTX was almost undetectable in the pharyngeal part throughout the maturation but was very abundant in the oocytes during spawning. 11-norTTX-6(S)-ol consistently localized in the pharyngeal tissue. Although the localization of TTX and its analogues was approximately consistent with the MS imaging data, TTX and 11-norTTX-6(S)-ol were found to be highly localized in the parenchyma surrounding the pharynx, which suggests the parenchyma is involved in the accumulation and production of TTXs., (© 2022. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.)
- Published
- 2022
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12. Mass spectrometry imaging reveals local metabolic changes in skeletal muscle due to chronic training.
- Author
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Goto-Inoue N, Morisasa M, Kimura K, Mori T, Furuichi Y, Manabe Y, and Fujii NL
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- Humans, Hypertrophy metabolism, Hypertrophy pathology, Mass Spectrometry, Muscular Atrophy metabolism, Muscle, Skeletal metabolism, Proteome metabolism
- Abstract
Muscle atrophy is a major health problem that needs effective prevention and treatment approaches. Chronic exercise, an effective treatment strategy for atrophy, promotes muscle hypertrophy, which leads to dynamic metabolic changes; however, the metabolic changes vary among myofiber types. To investigate local metabolic changes due to chronic exercise, we utilized comprehensive proteome and mass spectrometry (MS) imaging analyses. Our training model exhibited hypertrophic features only in glycolytic myofibers. The proteome analyses demonstrated that exercise promoted anabolic pathways, such as protein synthesis, and significant changes in lipid metabolism, but not in glucose metabolism. Furthermore, the fundamental energy sources, glycogen, neutral lipids, and ATP, were sensitive to exercise, and the changes in these sources differed between glycolytic and oxidative myofibers. MS imaging revealed that the lipid composition differs among myofibers; arachidonic acid might be an effective target for promoting lipid metabolism during muscle hypertrophy in oxidative myofibers., (© The Author(s) 2022. Published by Oxford University Press on behalf of Japan Society for Bioscience, Biotechnology, and Agrochemistry.)
- Published
- 2022
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13. A novel ND1 mitochondrial DNA mutation is maternally inherited in growth hormone transgenesis in amago salmon (Oncorhynchus masou ishikawae).
- Author
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Sato T, Goto-Inoue N, Kimishima M, Toyoharu J, Minei R, Ogura A, Nagoya H, and Mori T
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- Animals, Animals, Genetically Modified, DNA, Mitochondrial genetics, Female, Gene Transfer Techniques, Growth Hormone genetics, Mammals genetics, Maternal Inheritance, Mutation, Proteomics, Reactive Oxygen Species, Salmon genetics, Human Growth Hormone genetics, Oncorhynchus
- Abstract
Growth hormone (GH) transgenesis can be used to manipulate the growth performance of fish and mammals. In this study, homozygous and hemizygous GH-transgenic amago salmon (Oncorhynchus masou ishikawae) derived from a single female exhibited hypoglycemia. Proteomic and signal network analyses using iTRAQ indicated a decreased NAD
+ /NADH ratio in transgenic fish, indicative of reduced mitochondrial ND1 function and ROS levels. Mitochondrial DNA sequencing revealed that approximately 28% of the deletion mutations in the GH homozygous- and hemizygous-female-derived mitochondrial DNA occurred in ND1. These fish also displayed decreased ROS levels. Our results indicate that GH transgenesis in amago salmon may induce specific deletion mutations that are maternally inherited over generations and alter energy production., (© 2022. The Author(s).)- Published
- 2022
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14. Dietary Alaska Pollack Protein Induces Acute and Sustainable Skeletal Muscle Hypertrophy in Rats.
- Author
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Uchida K, Fujitani M, Mizushige T, Kawabata F, Hayamizu K, Uozumi K, Hara Y, Sawai M, Uehigashi R, Okada S, Goto-Inoue N, Morisasa M, and Kishida T
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- Alaska, Animals, Diet, High-Fat adverse effects, Hypertrophy, Male, Rats, Rats, Sprague-Dawley, Dietary Proteins pharmacology, Muscle, Skeletal metabolism
- Abstract
Our previous studies suggested that Alaska pollack protein (APP) intake increases skeletal muscle mass and that it may cause a slow-to-fast shift in muscle fiber type in rats fed a high-fat diet after 56 days of feeding. In this study, we explored whether dietary APP induces acute and sustainable skeletal muscle hypertrophy in rats fed a normal-fat diet. Male 5-week-old Sprague-Dawley rats were divided into four groups and fed a purified ingredient-based high-fat diet or a purified ingredient-based normal-fat diet with casein or APP, containing the same amount of crude protein. Dietary APP significantly increased gastrocnemius muscle mass (105~110%) after 2, 7 days of feeding, regardless of dietary fat content. Rats were separated into two groups and fed a normal-fat diet with casein or APP. Dietary APP significantly increased gastrocnemius muscle mass (110%) after 56 days of feeding. Dietary APP significantly increased the cross-sectional area of the gastrocnemius skeletal muscle and collagen-rich connective tissue after 7 days of feeding. It decreased the gene expression of Mstn /Myostatin, Trim63 /MuRF1, and Fbxo32 /atrogin-1, but not other gene expression, such as serum IGF-1 after 7 days of feeding. No differences were observed between casein and APP groups with respect to the percentage of Type I, Type IIA, and Type IIX or IIB fibers, as determined by myosin ATPase staining after 7 days of feeding. In the similar experiment, the puromycin-labeled peptides were not different between dietary casein and APP after 2 days of feeding. These results demonstrate that APP induces acute and sustainable skeletal muscle hypertrophy in rats, regardless of dietary fat content. Dietary APP, as a daily protein source, may be an approach for maintaining or increasing muscle mass.
- Published
- 2022
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15. Fish Protein Promotes Skeletal Muscle Hypertrophy via the Akt/mTOR Signaling Pathways.
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Morisasa M, Yoshida E, Fujitani M, Kimura K, Uchida K, Kishida T, Mori T, and Goto-Inoue N
- Subjects
- Animals, Hypertrophy metabolism, Male, Muscle, Skeletal metabolism, Myosin Heavy Chains metabolism, Protein Isoforms metabolism, Proteomics, Quality of Life, Rats, Signal Transduction, TOR Serine-Threonine Kinases metabolism, Fish Proteins metabolism, Proto-Oncogene Proteins c-akt metabolism
- Abstract
Skeletal muscle is the largest organ in the body and has a broad range of plasticity, undergoing atrophy in response to aging or disease and hypertrophy in response to nutritional supplements or exercise. Loss of skeletal muscle mass and force increases the risk of falls, impairs mobility, and leads to reduced quality of life. In a previous study, we demonstrated that taking in Alaska pollock protein (APP) for only 7 d increased the gastrocnemius muscle mass in rats. This study was conducted to identify hypertrophic myofibers and analyze how hypertrophy occurs within them. Twenty male rats were randomly divided into two groups and administered a diet of casein or APP for 7 d. The expression of each myosin heavy chain (MyHC) isoform in a cross-sectional area was then measured. MyHC IIb and IIx isoforms exhibited hypertrophic features in the gastrocnemius muscles of the APP-fed rats. Furthermore, comprehensive proteomic analyses were conducted to identify changes in protein expression due to muscle hypertrophy. Our results, evaluated by pathway analyses, indicated that the activity of the growth factor signaling pathway was significantly impacted by APP consumption. Moreover, APP could promote protein synthesis by activating the protein kinase B/mechanistic target of the rapamycin signaling pathway, which is also promoted by exercise.
- Published
- 2022
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16. Effect of antioxidant supplementation on skeletal muscle and metabolic profile in aging mice.
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Tsukamoto-Sen S, Kawakami S, Maruki-Uchida H, Ito R, Matsui N, Komiya Y, Mita Y, Morisasa M, Goto-Inoue N, Furuichi Y, Manabe Y, Morita M, and Fujii NL
- Subjects
- Animals, Antioxidants administration & dosage, Dietary Supplements, Mass Spectrometry, Mice, Motor Activity, Oxidative Stress drug effects, Aging drug effects, Antioxidants pharmacology, Muscle, Skeletal drug effects, Sarcopenia prevention & control
- Abstract
Aging induces drastic changes in muscle mass and function (sarcopenia); however, the detailed mechanisms underlying sarcopenia remain poorly understood. Recent studies suggested that age-related increases in oxidative stress induce muscle atrophy. In this study, we investigated the effect of 6-month supplementation of antioxidants, specifically piceatannol (PIC) and enzymatically modified isoquercitrin (EMIQ), on age-related physiological changes, including skeletal muscle weight and quality, in 25-month-old (OLD) mice, compared to in 4-month-old (young, YNG) C57BL/6J mice. Muscle weight corrected by body weight significantly declined in OLD mice, compared to in YNG mice. The control OLD mice also showed changes in the expression of genes related to muscle fiber type, reduced locomotor activity, and increased oxidative stress markers in blood. Consistent with the muscle weight and quality changes, whole-body fat oxidation during sedentary conditions and exercise periods in control OLD mice was significantly lower than that in YNG mice. Interestingly, compared to the control OLD mice, the PIC- or EMIQ-fed OLD mice showed higher fat oxidation. Furthermore, EMIQ, but not PIC, increased locomotor activity, the expression of genes encoding antioxidant enzymes, and suppressed the carbonylated protein in the skeletal muscle of OLD mice. These results suggested that chronic antioxidant intake could alleviate aging-related muscle function changes.
- Published
- 2021
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17. Lipid Dynamics due to Muscle Atrophy Induced by Immobilization.
- Author
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Kimura K, Morisasa M, Mizushige T, Karasawa R, Kanamaru C, Kabuyama Y, Hayasaka T, Mori T, and Goto-Inoue N
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- Animals, Chromatography, Liquid, Chromatography, Thin Layer, Cyclooxygenase 2 metabolism, Lipase metabolism, Male, Mass Spectrometry, Muscle, Skeletal chemistry, Phosphatidylcholines analysis, Phosphatidylserines analysis, Rats, Sprague-Dawley, Restraint, Physical adverse effects, Sphingomyelins analysis, Triglycerides analysis, Rats, Muscular Atrophy metabolism, Phosphatidylcholines metabolism, Phosphatidylserines metabolism, Restraint, Physical physiology, Sphingomyelins metabolism, Triglycerides metabolism
- Abstract
Muscle atrophy refers to skeletal muscle loss and dysfunction that affects glucose and lipid metabolism. Moreover, muscle atrophy is manifested in cancer, diabetes, and obesity. In this study, we focused on lipid metabolism during muscle atrophy. We observed that the gastrocnemius muscle was associated with significant atrophy with 8 days of immobilization of hind limb joints and that muscle atrophy occurred regardless of the muscle fiber type. Further, we performed lipid analyses using thin layer chromatography, liquid chromatography-mass spectrometry, and mass spectrometry imaging. Total amounts of triacylglycerol, phosphatidylserine, and sphingomyelin were found to be increased in the immobilized muscle. Additionally, we found that specific molecular species of phosphatidylserine, phosphatidylcholine, and sphingomyelin were increased by immobilization. Furthermore, the expression of adipose triglyceride lipase and the activity of cyclooxygenase-2 were significantly reduced by atrophy. From these results, it was revealed that lipid accumulation and metabolic changes in specific fatty acids occur during disuse muscle atrophy. The present study holds implications in validating preventive treatment strategies for muscle atrophy.
- Published
- 2021
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18. Novel approach to enhance sensitivity while retaining morphology in fragile tissue sections for mass spectrometry imaging.
- Author
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Goto-Inoue N, Morisasa M, Kimura K, and Mori T
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- Animals, Aquatic Organisms physiology, Larva cytology, Larva physiology, Ranidae, Sensitivity and Specificity, Histological Techniques methods, Molecular Imaging methods, Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization methods
- Abstract
Matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) imaging is an effective tool for investigating the distribution of molecules. However, cryosections are made from non-fixed tissues, causing difficulties in preparing sections from fragile, high-water content tissues such as those from tadpoles. Here, we introduce a new method for preparing cryosections using an adhesive tape followed by transfer onto glass slides for MALDI-MS imaging. Signals obtained from the transferred sections were higher than those from other sections, and the transferred sections had high optical quality. This novel approach could be an effective tool for MALDI-MS imaging of aquatic animals., (© 2020 John Wiley & Sons, Ltd.)
- Published
- 2020
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19. Amiodarone bioconcentration and suppression of metamorphosis in Xenopus.
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Sanoh S, Hanada H, Kashiwagi K, Mori T, Goto-Inoue N, Suzuki KT, Mori J, Nakamura N, Yamamoto T, Kitamura S, Kotake Y, Sugihara K, Ohta S, and Kashiwagi A
- Subjects
- Amiodarone metabolism, Animals, Endocrine Disruptors metabolism, Hindlimb drug effects, Larva genetics, Larva metabolism, Receptors, Thyroid Hormone genetics, Receptors, Thyroid Hormone metabolism, Triiodothyronine genetics, Triiodothyronine metabolism, Water Pollutants, Chemical metabolism, Xenopus laevis, Amiodarone toxicity, Bioaccumulation, Endocrine Disruptors toxicity, Gene Expression Regulation, Developmental drug effects, Larva drug effects, Water Pollutants, Chemical toxicity
- Abstract
Trace concentrations of a number of pharmaceutically active compounds have been detected in the aquatic environment in many countries, where they are thought to have the potential to exert adverse effects on non-target organisms. Amiodarone (AMD) is one such high-risk compound commonly used in general hospitals. AMD is known to alter normal thyroid hormone (TH) function, although little information is available regarding the specific mechanism by which this disruption occurs. Anuran tadpole metamorphosis is a TH-controlled developmental process and has proven to be useful as a screening tool for environmental pollutants suspected of disrupting TH functions. In the present study, our objective was to clarify the effects of AMD on Xenopus metamorphosis as well as to assess the bioconcentration of this pharmaceutical in the liver. We found that AMD suppressed spontaneous metamorphosis, including tail regression and hindlimb elongation in pro-metamorphic stage tadpoles, which is controlled by endogenous circulating TH, indicating that AMD is a TH antagonist. In transgenic X. laevis tadpoles carrying plasmid DNA containing TH-responsive element (TRE) and a 5'-upstream promoter region of the TH receptor (TR) βA1 gene linked to a green fluorescent protein (EGFP) gene, triiodothyronine (T
3 ) exposure induced a strong EGFP expression in the hind limbs, whereas the addition of AMD to T3 suppressed EGFP expression, suggesting that this drug interferes with the binding of T3 to TR, leading to the inhibition of TR-mediated gene expression. We also found AMD to be highly bioconcentrated in the liver of pro-metamorphic X. tropicalis tadpoles, and we monitored hepatic accumulation of this drug using mass spectrometry imaging (MSI). Our findings suggest that AMD imposes potential risk to aquatic wildlife by disrupting TH homeostasis, with further possibility of accumulating in organisms higher up in the food chain., (Copyright © 2020 Elsevier B.V. All rights reserved.)- Published
- 2020
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20. Effect of treatment with conditioned media derived from C2C12 myotube on adipogenesis and lipolysis in 3T3-L1 adipocytes.
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Tamura K, Goto-Inoue N, Miyata K, Furuichi Y, Fujii NL, and Manabe Y
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- 3T3 Cells, Adipocytes drug effects, Adipocytes metabolism, Adipogenesis, Adiponectin metabolism, Animals, Cell Communication, Culture Media, Conditioned pharmacology, Mice, PPAR gamma metabolism, Adipocytes cytology, Cell Differentiation, Lipolysis, Muscle Fibers, Skeletal metabolism
- Abstract
Regular exercise is an effective strategy that is used to prevent and treat obesity as well as type 2 diabetes. Exercise-induced myokine secretion is considered a mechanism that coordinates communication between muscles and other organs. In order to examine the possibility of novel communications from muscle to adipose tissue mediated by myokines, we treated 3T3-L1 adipocytes with C2C12 myotube electrical pulse stimulation-conditioned media (EPS-CM), using a C2C12 myotube contraction system stimulated by an electrical pulse. Continuous treatment with myotube EPS-CM promoted adipogenesis of 3T3-L1 pre-adipocytes via the upregulation of the peroxisome proliferator-activated receptor-gamma (PPARγ) 2 and PPARγ-regulated gene expression. Furthermore, our results revealed that myotube EPS-CM induces lipolysis and secretion of adiponectin in mature adipocytes. EPS-CM obtained from a C2C12 myoblast culture did not induce such changes in these genes, suggesting that contraction-induced myokine(s) secretion occurs particularly in differentiated myotubes. Thus, contraction-induced secretion of myokine(s) promotes adipogenesis and lipid metabolism in 3T3-L1 adipocytes. These findings suggest the possibility that skeletal muscle communicates to adipose tissues during exercise, probably by the intermediary of unidentified myokines., Competing Interests: The authors have declared that no competing interests exist.
- Published
- 2020
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21. Predation threats for a 24-h period activated the extension of axons in the brains of Xenopus tadpoles.
- Author
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Mori T, Kitani Y, Hatakeyama D, Machida K, Goto-Inoue N, Hayakawa S, Yamamoto N, Kashiwagi K, and Kashiwagi A
- Subjects
- Animals, Biomarkers, Gene Expression Profiling, Gene Expression Regulation, In Situ Hybridization, Larva, Signal Transduction, Axons physiology, Brain physiology, Xenopus laevis physiology
- Abstract
The threat of predation is a driving force in the evolution of animals. We have previously reported that Xenopus laevis enhanced their tail muscles and increased their swimming speeds in the presence of Japanese larval salamander predators. Herein, we investigated the induced gene expression changes in the brains of tadpoles under the threat of predation using 3'-tag digital gene expression profiling. We found that many muscle genes were expressed after 24 h of exposure to predation. Ingenuity pathway analysis further showed that after 24 h of a predation threat, various signal transduction genes were stimulated, such as those affecting the actin cytoskeleton and CREB pathways, and that these might increase microtubule dynamics, axonogenesis, cognition, and memory. To verify the increase in microtubule dynamics, DiI was inserted through the tadpole nostrils. Extension of the axons was clearly observed from the nostril to the diencephalon and was significantly increased (P ≤ 0.0001) after 24 h of exposure to predation, compared with that of the control. The dynamic changes in the signal transductions appeared to bring about new connections in the neural networks, as suggested by the microtubule dynamics. These connections may result in improved memory and cognition abilities, and subsequently increase survivability.
- Published
- 2020
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22. Application of Matrix-Assisted Laser Desorption/Ionization Mass Spectrometry Imaging for Evaluating the Quality of Fish Fillets.
- Author
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Morisasa M, Kimura K, Sumida M, Fukumoto S, Tamura T, Takeuchi R, Mori T, and Goto-Inoue N
- Abstract
Consumption of fish is rapidly increasing worldwide. It is important to evaluate fish fillet quality because fish undergoes physical and chemical changes during frozen storage. Fish fillets exhibit formaldehyde (FA) accumulation from the decomposition of trimethylamine N-oxide. FA is a powerful protein denaturant; thus, it is important to avoid FA buildup during fish processing to preserve fish quality, especially texture. To determine where FA accumulates, in order to maintain the quality of fish fillets, we performed matrix-assisted laser desorption/ionization mass spectrometry imaging, aiming to identify muscle-derived peptides, which reflect conditions such as denaturation and/or aggregation. We used frozen sections from which lipophilic molecules were washed out and detected various peptide peaks. Furthermore, we tried to identify indices to represent fish fillet softening by protease treatment. We could detect characteristic peaks owing to FA and protease treatment; the findings were consistent with the results of texture profiles showing fish fillet's real solidity. These molecules might thus serve as effective markers to evaluate fish fillet quality.
- Published
- 2020
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23. Mass spectrometry imaging reveals differential localization of natural sunscreens in the mantle of the giant clam Tridacna crocea.
- Author
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Goto-Inoue N, Sato T, Morisasa M, Yamashita H, Maruyama T, Ikeda H, and Sakai R
- Subjects
- Animals, Sunscreening Agents analysis, Ultraviolet Rays, Bivalvia metabolism, Chromatography, Liquid methods, Cyclohexanols metabolism, Mass Spectrometry methods, Sunscreening Agents metabolism
- Abstract
Giant clams have evolved to maximize sunlight utilization by their photosymbiotic partners, while affording them protection from harmful ultraviolet (UV) light. The presence of UV absorbing substances in the mantle is thought to be critical for light protection; however, the exact localization of such compounds remains unknown. Here, we applied a combination of UV liquid chromatography (LC), LC-mass spectrometry (MS), MS imaging, and UV micrography to localize UV absorbing substances in the giant clam Tridacna crocea. LC-MS analysis revealed that the animal contained three classes of mycosporines: progenitor, primary, and secondary mycosporines. MS imaging revealed that primary and secondary mycosporines were localized in the outermost layer of the mantle; whereas progenitor mycosporines were distributed throughout the mantle tissue. These findings were consistent with the results of UV micrography, which revealed that the surface layer of the mantle absorbed UV light at 320 ± 10 nm. This is the first report indicating that progenitor and primary mycosporines are metabolized to secondary mycosporines by the giant clam and that they are differentially localized in the surface layer of the mantle to protect the animal from UV light.
- Published
- 2020
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24. Application of Matrix-Assisted Laser Desorption/Ionization Mass Spectrometry Imaging for Food Analysis.
- Author
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Morisasa M, Sato T, Kimura K, Mori T, and Goto-Inoue N
- Abstract
Food contains various compounds, and there are many methods available to analyze each of these components. However, the large amounts of low-molecular-weight metabolites in food, such as amino acids, organic acids, vitamins, lipids, and toxins, make it difficult to analyze the spatial distribution of these molecules. Matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) imaging is a two-dimensional ionization technology that allows the detection of small metabolites in tissue sections without requiring purification, extraction, separation, or labeling. The application of MALDI-MS imaging in food analysis improves the visualization of these compounds to identify not only the nutritional content but also the geographical origin of the food. In this review, we provide an overview of some recent applications of MALDI-MS imaging, demonstrating the advantages and prospects of this technology compared to conventional approaches. Further development and enhancement of MALDI-MS imaging is expected to offer great benefits to consumers, researchers, and food producers with respect to breeding improvement, traceability, the development of value-added foods, and improved safety assessments., Competing Interests: The authors declare no conflicts of interest
- Published
- 2019
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25. Characterization of Metabolite Compositions in Wild and Farmed Red Sea Bream ( Pagrus major) Using Mass Spectrometry Imaging.
- Author
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Goto-Inoue N, Sato T, Morisasa M, Igarashi Y, and Mori T
- Subjects
- Animals, Animals, Wild metabolism, Chromatography, Thin Layer, Discriminant Analysis, Fatty Acids chemistry, Fatty Acids metabolism, Fish Proteins chemistry, Fish Proteins metabolism, Fisheries, Mass Spectrometry methods, Muscle, Skeletal chemistry, Muscle, Skeletal metabolism, Triglycerides chemistry, Triglycerides metabolism, Sea Bream metabolism, Seafood analysis
- Abstract
Nutritional profiles and consumer preferences differ between wild and farmed fish, and identification of fish sources can be difficult. We analyzed the metabolite molecules of wild and farmed red sea bream ( Pagrus major) to identify specific metabolic differences. The total lipid content and molecular composition of wild and farmed red sea bream muscles were analyzed using thin-layer chromatography and mass spectrometry imaging. Triacylglycerol levels were significantly higher in farmed fish. Wild fish contained saturated-fatty-acid-containing triacylglycerols as a major molecular species, while docosahexaenoic-acid-containing triacylglycerol levels were significantly higher in farmed fish than in wild fish. The localization of each muscle-fiber-type-specific marker demonstrated that wild fish exhibit myosin heavy chain (MHC)-type-IIb-specific phospholipids, while farmed fish exhibit MHC-type-IIa-specific phospholipids in their white muscle. Sodium dodecyl sulfate polyacrylamide gel electrophoresis analyses separated the identified myosins and revealed that farmed fish possess additional myosin isoforms when compared to wild fish. In addition, we found a farmed-fish-specific distribution of anserine in their white muscle. These molecules can be used as new molecular markers for determining the geographic origins of wild versus farmed red sea bream.
- Published
- 2019
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26. Characterization of myofiber-type-specific molecules using mass spectrometry imaging.
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Goto-Inoue N, Morisasa M, Machida K, Furuichi Y, Fujii NL, Miura S, and Mori T
- Subjects
- Animals, Biomarkers metabolism, Chromatography, Thin Layer, Diglycerides analysis, Diglycerides metabolism, Image Processing, Computer-Assisted, Lipids analysis, Male, Mice, Inbred ICR, Muscle Fibers, Skeletal metabolism, Muscle, Skeletal chemistry, Muscle, Skeletal metabolism, Muscle, Smooth chemistry, Muscle, Smooth metabolism, Tandem Mass Spectrometry, Biomarkers analysis, Muscle Fibers, Skeletal chemistry, Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization methods
- Abstract
Rationale: In skeletal muscles, there are four myofiber types, Types I, IIa, IIx, and IIb, which show different contraction characteristics and have different metabolic statuses. To understand muscle function, it is necessary to analyze myofiber-specific metabolic changes. However, these fibers are heterogeneous and are hard to discriminate by conventional analyses using tissue extracts. In this study, we found myofiber-specific molecules and molecular markers of other cells such as smooth muscle cells, fat cells, and motor neurons, and visualized them within muscle sections., Methods: We used three different muscle tissues, namely extensor digitorum longus, soleus, and gastrocnemius tissues, from ICR mice. After the muscles had been harvested, cross-sections were prepared using a cryostat and analyzed using matrix-assisted laser desorption/ionization (MALDI) mass spectrometry imaging (MSI), and conventional immunofluorescence imaging., Results: By comparing the MALDI MSI results with the immunofluorescence imaging results, we were able to identify each fiber and cell-specific ion. It was especially important that we could find Type IIa and IIb specific ions, because these were difficult to distinguish., Conclusions: Through MSI analyses, we performed a comprehensive survey to identify cell- and myofiber-specific molecular markers. In conclusion, we assigned muscle fiber Type I, IIa, and IIb-specific molecular ions at m/z 856.6, 872.6, and 683.8, respectively. These molecular markers might be useful for verifying changes that occur due to exercise and/or disease., (© 2018 John Wiley & Sons, Ltd.)
- Published
- 2019
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27. Investigation of the Lipid Changes That Occur in Hypertrophic Muscle due to Fish Protein-feeding Using Mass Spectrometry Imaging.
- Author
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Morisasa M, Goto-Inoue N, Sato T, Machida K, Fujitani M, Kishida T, Uchida K, and Mori T
- Subjects
- Animals, Gadiformes, Male, Muscle Fibers, Fast-Twitch metabolism, Muscle Fibers, Slow-Twitch metabolism, Muscle, Skeletal abnormalities, Rats, Sprague-Dawley, Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization, Fish Proteins administration & dosage, Hypertrophy, Lipid Metabolism, Lipids analysis, Muscle, Skeletal metabolism
- Abstract
Alaska pollack protein (APP) was previously shown to reduce serum triacylglycerol and the atherogenic index and significantly increase gastrocnemius muscle mass in rats. To determine which myofibers are involved in this observed hypertrophy, we stained the gastrocnemius muscle with fast and slow fiber-specific antibodies and measured the muscle fiber diameter. We observed muscle hypertrophy in both the fast and slow fibers of APP-fed rats. Although muscle hypertrophy leads to drastic lipid changes, the amount of lipids did not differ significantly between casein-fed and APP-fed rats. To determine the lipid changes at the molecular species level and their localization, we performed matrix-assisted laser desorption/ionization mass spectrometry imaging to visualize lipids in the gastrocnemius muscles. We determined that lipid molecules were significantly changed due to APP feeding. Thus, APP feeding changes muscle lipid metabolism, and these metabolic changes might be related to hypertrophy.
- Published
- 2019
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28. Properties, metabolism and roles of sulfogalactosylglycerolipid in male reproduction.
- Author
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Tanphaichitr N, Kongmanas K, Faull KF, Whitelegge J, Compostella F, Goto-Inoue N, Linton JJ, Doyle B, Oko R, Xu H, Panza L, and Saewu A
- Subjects
- Animals, Fertility physiology, Galactolipids biosynthesis, Homeostasis physiology, Humans, Male, Sertoli Cells cytology, Sertoli Cells metabolism, Galactolipids metabolism, Reproduction physiology, Spermatogenesis physiology, Spermatozoa metabolism
- Abstract
Sulfogalactosylglycerolipid (SGG, aka seminolipid) is selectively synthesized in high amounts in mammalian testicular germ cells (TGCs). SGG is an ordered lipid and directly involved in cell adhesion. SGG is indispensable for spermatogenesis, a process that greatly depends on interaction between Sertoli cells and TGCs. Spermatogenesis is disrupted in mice null for Cgt and Cst, encoding two enzymes essential for SGG biosynthesis. Sperm surface SGG also plays roles in fertilization. All of these results indicate the significance of SGG in male reproduction. SGG homeostasis is also important in male fertility. Approximately 50% of TGCs become apoptotic and phagocytosed by Sertoli cells. SGG in apoptotic remnants needs to be degraded by Sertoli lysosomal enzymes to the lipid backbone. Failure in this event leads to a lysosomal storage disorder and sub-functionality of Sertoli cells, including their support for TGC development, and consequently subfertility. Significantly, both biosynthesis and degradation pathways of the galactosylsulfate head group of SGG are the same as those of sulfogalactosylceramide (SGC), a structurally related sulfoglycolipid important for brain functions. If subfertility in males with gene mutations in SGG/SGC metabolism pathways manifests prior to neurological disorder, sperm SGG levels might be used as a reporting/predicting index of the neurological status., (Copyright © 2018 Elsevier Ltd. All rights reserved.)
- Published
- 2018
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29. Utilizing mass spectrometry imaging to map the thyroid hormones triiodothyronine and thyroxine in Xenopus tropicalis tadpoles.
- Author
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Goto-Inoue N, Sato T, Morisasa M, Kashiwagi A, Kashiwagi K, Sugiura Y, Sugiyama E, Suematsu M, and Mori T
- Subjects
- Animals, Spectroscopy, Fourier Transform Infrared, Larva metabolism, Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization methods, Tandem Mass Spectrometry methods, Thyroxine metabolism, Triiodothyronine metabolism, Xenopus growth & development
- Abstract
Thyroid hormones are not only responsible for thermogenesis and energy metabolism in animals, but also have an important role in cell differentiation and development. Amphibian metamorphosis provides an excellent model for studying the remodeling of the body. This metamorphic organ remodeling is induced by thyroid hormones, and a larval body is thus converted into an adult one. The matrix-assisted laser desorption/ionization (MALDI)-mass spectrometry (MS) imaging technology is expected to be a suitable tool for investigating small bioreactive molecules. The present study describes the distribution of the thyroid hormones, i.e., triiodothyronine (T3) and thyroxine (T4) and their inactive form reverse T3 (rT3) in Xenopus tropicalis tadpoles using two different types of imaging techniques, MS/MS and Fourier transform (FT)-MS imaging. As a result of MS/MS imaging, we demonstrated that T3 was mainly distributed in the gills. T4 was faintly localized in the eyes, inner gills, and intestine during metamorphosis. The intensity of T3 in the gills and the intensity of T4 in the body fluids were increased during metamorphosis. Moreover, the localization of the inactive form rT3 was demonstrated to be separate from T3, namely in the intestine and muscles. In addition, FT-MS imaging could utilize simultaneous imaging including thyroid hormone. This is the first report to demonstrate the molecular distribution of thyroid hormones themselves and to discriminate T3, T4, and rT3 in animal tissues.
- Published
- 2018
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30. Correction: The constant threat from a non-native predator increases tail muscle and fast-start swimming performance in Xenopus tadpoles.
- Author
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Mori T, Yanagisawa Y, Kitani Y, Yamamoto G, Goto-Inoue N, Kimura T, Kashiwagi K, and Kashiwagi A
- Published
- 2018
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31. The constant threat from a non-native predator increases tail muscle and fast-start swimming performance in Xenopus tadpoles.
- Author
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Mori T, Yanagisawa Y, Kitani Y, Yamamoto G, Goto-Inoue N, Kimura T, Kashiwagi K, and Kashiwagi A
- Abstract
Predator-induced phenotypic plasticity is the ability of prey to adapt to their native predator. However, owing to environmental changes, encounters with unknown predators are inevitable. Therefore, study of prey and non-native predator interaction will reveal the primary stages of adaptive strategies in prey-predator interactions in the context of evolutionary processes. Here, Xenopus tadpoles exposed to a non-native predator, a larval salamander, showed a significant increase in body weight and tail length to body length ratio. The T
max 2 test indicated a significant enhancement of the tail muscle and decrease in the relative ventral fin height in tadpoles exposed to predation risk, leading to significantly higher average swimming speeds. The analysis of muscle-related metabolites revealed that sarcosine increased significantly in tadpoles exposed to non-native predators. Multiple linear regression analysis of the fast-start swimming pattern showed that the fast-start swimming speed was determined by the time required for a tadpole to bend its body away from the threat (C-start) and the angle at which it was bent. In conclusion, morphological changes in tadpoles were functionally adaptive and induced by survival behaviors of Xenopus tadpoles against non-native predators., Competing Interests: Competing interestsThe authors declare no competing or financial interests., (© 2017. Published by The Company of Biologists Ltd.)- Published
- 2017
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32. Immunohistochemical expression analysis of leucine-rich PPR-motif-containing protein (LRPPRC), a candidate colorectal cancer biomarker identified by shotgun proteomics using iTRAQ.
- Author
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Nishio T, Kurabe N, Goto-Inoue N, Nakamura T, Sugimura H, Setou M, and Maekawa M
- Subjects
- Adult, Aged, Aged, 80 and over, Biomarkers, Tumor biosynthesis, Colorectal Neoplasms metabolism, Female, Humans, Immunohistochemistry, Male, Middle Aged, Neoplasm Proteins biosynthesis, Biomarkers, Tumor analysis, Colorectal Neoplasms diagnosis, Neoplasm Proteins analysis, Proteomics
- Abstract
Background: Colorectal cancer (CRC) is the fourth most frequent cause of cancer deaths in the world. Novel biomarkers for the diagnosis, prognosis, and treatment of CRC are required to improve the clinical strategy., Methods: We applied shotgun proteomics using isobaric tags for relative and absolute quantitation (iTRAQ) to identify novel biomarkers of CRC, and then we detected leucine-rich PPR-motif-containing protein (LRPPRC) expression in 83 normal colorectal tissues and 133 CRC tissues by immunohistochemistry., Results: A total of 570 proteins were identified using iTRAQ. We validated the expression of LRPPRC protein by immunohistochemical analysis of the 77 proteins that showed expression changes in the cancer tissues >1.5-fold the levels in the normal tissues. The expression levels of LRPPRC were significantly higher in CRC tissues than those in normal colorectal tissues, and the expression levels were related with tumor differentiation and especially high in moderately differentiated CRC tissues., Conclusion: We identified a novel, differentially expressed protein, LRPPRC, which has the potential to serve as a molecular target for diagnosis and/or prognosis of CRC., (Copyright © 2017 Elsevier B.V. All rights reserved.)
- Published
- 2017
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33. Minos-insertion mutant of the Drosophila GBA gene homologue showed abnormal phenotypes of climbing ability, sleep and life span with accumulation of hydroxy-glucocerebroside.
- Author
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Kawasaki H, Suzuki T, Ito K, Takahara T, Goto-Inoue N, Setou M, Sakata K, and Ishida N
- Subjects
- DNA Transposable Elements genetics, Drosophila Proteins genetics, Drosophila Proteins metabolism, Gaucher Disease genetics, Gaucher Disease metabolism, Gene Expression Regulation, Enzymologic, Glucosylceramidase metabolism, Humans, Isoenzymes genetics, Isoenzymes metabolism, Mutagenesis, Insertional, Phenotype, RNA Interference, Reverse Transcriptase Polymerase Chain Reaction, Glucosylceramidase genetics, Glucosylceramides metabolism, Longevity genetics, Motor Activity genetics, Mutation, Sleep genetics
- Abstract
Gaucher's disease in humans is considered a deficiency of glucocerebrosidase (GlcCerase) that result in the accumulation of its substrate, glucocerebroside (GlcCer). Although mouse models of Gaucher's disease have been reported from several laboratories, these models are limited due to the perinatal lethality of GlcCerase gene. Here, we examined phenotypes of Drosophila melanogaster homologues genes of the human Gaucher's disease gene by using Minos insertion. One of two Minos insertion mutants to unknown function gene (CG31414) accumulates the hydroxy-GlcCer in whole body of Drosophila melanogaster. This mutant showed abnormal phenotypes of climbing ability and sleep, and short lifespan. These abnormal phenotypes are very similar to that of Gaucher's disease in human. In contrast, another Minos insertion mutant (CG31148) and its RNAi line did not show such severe phenotype as observed in CG31414 gene mutation. The data suggests that Drosophila CG31414 gene mutation might be useful for unraveling the molecular mechanism of Gaucher's disease., (Copyright © 2017 Elsevier B.V. All rights reserved.)
- Published
- 2017
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34. Significant advancement of mass spectrometry imaging for food chemistry.
- Author
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Yoshimura Y, Goto-Inoue N, Moriyama T, and Zaima N
- Subjects
- Food Analysis instrumentation, Food Technology instrumentation, Food Technology trends, Mass Spectrometry instrumentation, Food Analysis methods, Food Technology methods, Mass Spectrometry methods
- Abstract
Food contains various compounds that have an impact on our daily lives. Many technologies have been established to analyze these molecules of interest in foods. However, the analysis of the spatial distribution of these compounds in foods using conventional technology, such as high-performance liquid chromatography-mass spectrometry or gas chromatography-mass spectrometry is difficult. Matrix-assisted laser desorption/ionization mass spectrometry imaging (MALDI-MSI) is considered an ideal complementary approach. MALDI-MSI is a two-dimensional MALDI-MS technology that can detect compounds in a tissue section without extraction, purification, separation, or labeling. MALDI-MSI can be used to visualize the spatial distribution of chemical compounds or biomolecules in foods. Although the methodology of MALDI-MSI in food science is not yet fully established, the versatility of MALDI-MSI is expected to open a new frontier in food science. Herein, we describe the principles and applications of MALDI-MSI in food science and related fields., (Copyright © 2016 Elsevier Ltd. All rights reserved.)
- Published
- 2016
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35. Metabolomic approach for identifying and visualizing molecular tissue markers in tadpoles of Xenopus tropicalis by mass spectrometry imaging.
- Author
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Goto-Inoue N, Kashiwagi A, Kashiwagi K, and Mori T
- Abstract
In developmental and cell biology it is crucial to evaluate the dynamic profiles of metabolites. An emerging frog model system using Xenopus tropicalis, whose genome sequence and inbred strains are available, is now ready for metabolomics investigation in amphibians. In this study we applied matrix-assisted laser desorption/ionization (MALDI)-mass spectrometry imaging (MSI) analysis to identify and visualize metabolomic molecular markers in tadpoles of Xenopus tropicalis We detected tissue-specific peaks and visualized their distribution in tissues, and distinguished 19 tissues and their specific peaks. We identified, for the first time, some of their molecular localizations via tandem mass spectrometric analysis: hydrocortisone in artery, L-DOPA in rhombencephalon, taurine in eye, corticosterone in gill, heme in heart, inosine monophosphate and carnosine in muscle, dopamine in nerves, and phosphatidylethanolamine (16:0/20:4) in pharynx. This is the first MALDI-MSI study of X. tropicalis tadpoles, as in small tadpoles it is hard to distinguish and dissect the various organs. Furthermore, until now there has been no data about the metabolomic profile of each organ. Our results suggest that MALDI-MSI is potentially a powerful tool for examining the dynamics of metabolomics in metamorphosis as well as conformational changes due to metabolic changes., Competing Interests: The authors declare no competing or financial interests., (© 2016. Published by The Company of Biologists Ltd.)
- Published
- 2016
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36. Evaluation of an in vitro muscle contraction model in mouse primary cultured myotubes.
- Author
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Manabe Y, Ogino S, Ito M, Furuichi Y, Takagi M, Yamada M, Goto-Inoue N, Ono Y, and Fujii NL
- Subjects
- Animals, Cell Differentiation, Cell Line, Cells, Cultured, Electron Transport Complex IV analysis, Mice, Muscle Fibers, Skeletal ultrastructure, Muscle, Skeletal cytology, Muscle, Skeletal ultrastructure, Myoglobin analysis, Myosin Heavy Chains analysis, Sarcomeres ultrastructure, Muscle Contraction, Muscle Fibers, Skeletal cytology, Muscle, Skeletal physiology
- Abstract
To construct an in vitro contraction model with the primary cultured myotubes, we isolated satellite cells from the mouse extensor digitorum longus. Differentiated myotubes possessed a greater number of sarcomere assemblies and higher expression levels of myosin heavy chain, cytochrome c oxidase IV, and myoglobin than in C2C12 myotubes. In agreement with these results regarding the sarcomere assemblies and protein expressions, the primary myotubes showed higher contractile activity stimulated by the electric pulses than that in the C2C12 myotubes. These data suggest that mouse primary myotubes will be a valuable research tool as an in vitro muscle contraction model., (Copyright © 2015 Elsevier Inc. All rights reserved.)
- Published
- 2016
- Full Text
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37. A fragmented form of annexin A1 is secreted from C2C12 myotubes by electric pulse-induced contraction.
- Author
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Goto-Inoue N, Tamura K, Motai F, Ito M, Miyata K, Manabe Y, and Fujii NL
- Subjects
- Animals, Annexin A1 chemistry, Cell Line, Mass Spectrometry, Mice, Wound Healing, Annexin A1 metabolism, Electricity, Muscle Fibers, Skeletal metabolism
- Abstract
The main function of annexin A1 (ANXA1), a member of the annexin superfamily, is to bind to cellular membranes in a Ca(2+)-dependent manner. In skeletal muscle, ANXA1 is thought to be involved in the repair of damaged membrane tissue and in the migration of muscle cells. We hypothesized that ANXA1 is one of the myokines secreted during muscle contractions to accelerate the repair of cell damage after contraction. Here we performed cell contractions by electric pulse stimulation; the results revealed that a fragmented form of ANXA1 was cleaved by calpain and selectively secreted from skeletal muscle cells by contraction. We therefore realized that muscle-contraction-induced calpain-dependent ANXA1 fragmentation has a wound-healing effect on damaged cells. This suggested that not the intact form but rather fragmented ANXA1 is a contraction-induced myokine.
- Published
- 2016
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38. PGC-1α-mediated changes in phospholipid profiles of exercise-trained skeletal muscle.
- Author
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Senoo N, Miyoshi N, Goto-Inoue N, Minami K, Yoshimura R, Morita A, Sawada N, Matsuda J, Ogawa Y, Setou M, Kamei Y, and Miura S
- Subjects
- Animals, Humans, Male, Mass Spectrometry, Mice, Mice, Transgenic, Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha, Transcription Factors genetics, Muscle, Skeletal metabolism, Phospholipids metabolism, Physical Conditioning, Animal physiology, Transcription Factors metabolism
- Abstract
Exercise training influences phospholipid fatty acid composition in skeletal muscle and these changes are associated with physiological phenotypes; however, the molecular mechanism of this influence on compositional changes is poorly understood. Peroxisome proliferator-activated receptor γ coactivator 1α (PGC-1α), a nuclear receptor coactivator, promotes mitochondrial biogenesis, the fiber-type switch to oxidative fibers, and angiogenesis in skeletal muscle. Because exercise training induces these adaptations, together with increased PGC-1α, PGC-1α may contribute to the exercise-mediated change in phospholipid fatty acid composition. To determine the role of PGC-1α, we performed lipidomic analyses of skeletal muscle from genetically modified mice that overexpress PGC-1α in skeletal muscle or that carry KO alleles of PGC-1α. We found that PGC-1α affected lipid profiles in skeletal muscle and increased several phospholipid species in glycolytic muscle, namely phosphatidylcholine (PC) (18:0/22:6) and phosphatidylethanolamine (PE) (18:0/22:6). We also found that exercise training increased PC (18:0/22:6) and PE (18:0/22:6) in glycolytic muscle and that PGC-1α was required for these alterations. Because phospholipid fatty acid composition influences cell permeability and receptor stability at the cell membrane, these phospholipids may contribute to exercise training-mediated functional changes in the skeletal muscle., (Copyright © 2015 by the American Society for Biochemistry and Molecular Biology, Inc.)
- Published
- 2015
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39. Hypoperfusion of the Adventitial Vasa Vasorum Develops an Abdominal Aortic Aneurysm.
- Author
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Tanaka H, Zaima N, Sasaki T, Sano M, Yamamoto N, Saito T, Inuzuka K, Hayasaka T, Goto-Inoue N, Sugiura Y, Sato K, Kugo H, Moriyama T, Konno H, Setou M, and Unno N
- Subjects
- Aged, Animals, Aorta, Abdominal metabolism, Aorta, Abdominal pathology, Aorta, Abdominal physiopathology, Aortic Aneurysm, Abdominal complications, Aortic Aneurysm, Abdominal metabolism, Aortic Aneurysm, Abdominal pathology, Constriction, Pathologic complications, Female, Humans, Male, Oxygen metabolism, Rats, Rats, Sprague-Dawley, Vasa Vasorum metabolism, Vasa Vasorum pathology, Aortic Aneurysm, Abdominal physiopathology, Blood Circulation, Vasa Vasorum physiopathology
- Abstract
The aortic wall is perfused by the adventitial vasa vasorum (VV). Tissue hypoxia has previously been observed as a manifestation of enlarged abdominal aortic aneurysms (AAAs). We sought to determine whether hypoperfusion of the adventitial VV could develop AAAs. We created a novel animal model of adventitial VV hypoperfusion with a combination of a polyurethane catheter insertion and a suture ligation of the infrarenal abdominal aorta in rats. VV hypoperfusion caused tissue hypoxia and developed infrarenal AAA, which had similar morphological and pathological characteristics to human AAA. In human AAA tissue, the adventitial VV were stenotic in both small AAAs (30-49 mm in diameter) and in large AAAs (> 50 mm in diameter), with the sac tissue in these AAAs being ischemic and hypoxic. These results indicate that hypoperfusion of adventitial VV has critical effects on the development of infrarenal AAA.
- Published
- 2015
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40. Correction: Expression of Human Gaucher Disease Gene GBA Generates Neurodevelopmental Defects and ER Stress in Drosophila Eye.
- Author
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Suzuki T, Shimoda M, Ito K, Hanai S, Aizawa H, Kato T, Kawasaki K, Yamaguchi T, Ryoo HD, Goto-Inoue N, Setou M, Tsuji S, and Ishida N
- Published
- 2015
- Full Text
- View/download PDF
41. Imaging Mass Spectrometry Reveals a Unique Distribution of Triglycerides in the Abdominal Aortic Aneurysmal Wall.
- Author
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Tanaka H, Zaima N, Sasaki T, Yamamoto N, Inuzuka K, Sano M, Saito T, Hayasaka T, Goto-Inoue N, Sato K, Kugo H, Moriyama T, Konno H, Setou M, and Unno N
- Subjects
- Adipocytes chemistry, Adipocytes pathology, Adventitia chemistry, Adventitia pathology, Aged, Aorta, Abdominal pathology, Aorta, Abdominal surgery, Aortic Aneurysm, Abdominal pathology, Aortic Aneurysm, Abdominal surgery, Collagen analysis, Female, Humans, Male, Middle Aged, PPAR gamma analysis, Stem Cells chemistry, Stem Cells pathology, Aorta, Abdominal chemistry, Aortic Aneurysm, Abdominal metabolism, Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization, Triglycerides analysis
- Abstract
The pathophysiology underlying abdominal aortic aneurysms (AAAs) remains unknown. In this study, we applied imaging mass spectrometry (IMS) to analyze the pathophysiology of the aneurysmal wall. Comparisons were performed between the tissue samples from the neck and the sac of the AAA, at a single time point, in 30 patients who underwent elective surgery of their AAAs. The localization of each lipid molecule in the aortic wall was assessed by IMS. Histopathological examination and IMS revealed a characteristic distribution of triglycerides (TGs) specifically in the aneurismal adventitia of the sac. This characteristic TG distribution was derived from an ectopic appearance of adipocytes in the adventitia. Furthermore, ectopic adipocyte accumulation in the aortic wall leads to the loss of the collagen fiber network subsequent to the wall rupture. The underlying mechanism of adipocyte accumulation involves the presence of adipose-derived stem cells (ADSCs) in the aneurismal adventitia and the expression of peroxisome proliferator-activated receptor gamma 2, a master regulator of adipocyte differentiation by some ADSCs. This study reveals new, previously overlooked aspects of AAA pathology., (© 2015 S. Karger AG, Basel.)
- Published
- 2015
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42. Redox proteins are constitutively secreted by skeletal muscle.
- Author
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Manabe Y, Takagi M, Nakamura-Yamada M, Goto-Inoue N, Taoka M, Isobe T, and Fujii NL
- Subjects
- Animals, Cell Line, Exosomes metabolism, Glutaredoxins metabolism, Mice, Oxidation-Reduction, Peroxiredoxins metabolism, Secretory Vesicles metabolism, Muscle Fibers, Skeletal metabolism, Muscle, Skeletal metabolism, Thioredoxins metabolism
- Abstract
Myokines are skeletal muscle-derived hormones. In this study, using a C2C12 myotube contraction system, we sought to determine whether the skeletal muscle secreted thioredoxin (TRX) and related redox proteins. Redox proteins such as TRXs, peroxiredoxins, and glutaredoxins were detected in the C2C12 myotube culture medium in the absence of any stimulation. The amounts of TRXs, peroxiredoxins, and glutaredoxins secreted by the C2C12 myotubes were not affected by the contraction, unless the myotubes were injured. Because TRX-1 was known to be a secreted protein that lacks a signal peptide, we examined whether this protein was secreted via exosome vesicles. The results indicated that TRX-1 was not secreted via exosome vesicles. We concluded that TRX-1 and related redox proteins are myokines that are constitutively secreted by the skeletal muscle cells. Although the mechanism of TRX-1 secretion remains unclear, our findings suggest that the skeletal muscle is an endocrine organ and the redox proteins that are constitutively secreted from the skeletal muscle may exert antioxidant and systemic health-promoting effects.
- Published
- 2014
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43. Imaging mass spectrometry reveals fiber-specific distribution of acetylcarnitine and contraction-induced carnitine dynamics in rat skeletal muscles.
- Author
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Furuichi Y, Goto-Inoue N, Manabe Y, Setou M, Masuda K, and Fujii NL
- Subjects
- Adenosine Triphosphate metabolism, Animals, Male, Muscle, Skeletal physiology, Rats, Rats, Wistar, Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization, Tandem Mass Spectrometry, Acetylcarnitine metabolism, Carnitine metabolism, Muscle Contraction, Muscle, Skeletal metabolism
- Abstract
Carnitine is well recognized as a key regulator of long-chain fatty acyl group translocation into the mitochondria. In addition, carnitine, as acetylcarnitine, acts as an acceptor of excess acetyl-CoA, a potent inhibitor of pyruvate dehydrogenase. Here, we provide a new methodology for accurate quantification of acetylcarnitine content and determination of its localization in skeletal muscles. We used matrix-assisted laser desorption/ionization imaging mass spectrometry (MALDI-IMS) to visualize acetylcarnitine distribution in rat skeletal muscles. MALDI-IMS and immunohistochemistry of serial cross-sections showed that acetylcarnitine was enriched in the slow-type muscle fibers. The concentration of ATP was lower in muscle regions with abundant acetylcarnitine, suggesting a relationship between acetylcarnitine and metabolic activity. Using our novel method, we detected an increase in acetylcarnitine content after muscle contraction. Importantly, this increase was not detected using traditional biochemical assays of homogenized muscles. We also demonstrated that acetylation of carnitine during muscle contraction was concomitant with glycogen depletion. Our methodology would be useful for the quantification of acetylcarnitine and its contraction-induced kinetics in skeletal muscles., (Copyright © 2014 Elsevier B.V. All rights reserved.)
- Published
- 2014
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44. Matrix-assisted laser desorption/ionization imaging mass spectrometry: new technology for vascular pathology.
- Author
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Zaima N, Goto-Inoue N, and Moriyama T
- Subjects
- Animals, Biomarkers metabolism, Humans, Predictive Value of Tests, Prognosis, Vascular Diseases pathology, Lipid Metabolism, Molecular Imaging methods, Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization, Vascular Diseases metabolism
- Abstract
The use of matrix-assisted laser desorption/ionization imaging mass spectrometry (MALDI-IMS) for the assessment of vascular pathology is attracting attention as a new valuable tool for diagnosing disease and finding new markers. MALDI-IMS is a molecular imaging technique whereby the simultaneous measurement of multiple samples directly from clinical tissue sections is possible. The versatility of MALDI-IMS has opened a new frontier in vascular pathology. In this review, we describe the principle and applications of MALDI-IMS.
- Published
- 2014
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45. Lipidomics analysis revealed the phospholipid compositional changes in muscle by chronic exercise and high-fat diet.
- Author
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Goto-Inoue N, Yamada K, Inagaki A, Furuichi Y, Ogino S, Manabe Y, Setou M, and Fujii NL
- Subjects
- Animals, Glucose Tolerance Test, Male, Metabolomics methods, Phospholipids chemistry, Rats, Diet, High-Fat, Lipid Metabolism, Muscle, Skeletal metabolism, Phospholipids metabolism, Physical Conditioning, Animal
- Abstract
Although it is clear that lipids are responsible for insulin resistance, it is poorly understood what types of lipids are involved. In this study, we verified the characteristic lipid species in skeletal muscle of a chronic exercise training model and a high-fat induced-obesity model. Three different lipidomics analyses revealed phospholipid qualitative changes. As a result, linoleic acid-containing phosphatidylcholine and sphingomyelin and docosahexanoic acid-containing phosphatidylcholine were characterized as chronic exercise training-induced lipids. On the contrary, arachidonic acid-containing phosphatidylcholines, phosphatidylethanolamines, and phosphatidylinositol were characterized as high-fat diet-induced lipids. In addition, minor sphingomyelin, which has long-chain fatty acids, was identified as a high-fat diet-specific lipid. This is the first report to reveal compositional changes in phospholipid molecular species in chronic exercise and high-fat-diet-induced insulin-resistant models. Due to their influence on cell permeability and receptor stability at the cell membrane, these molecules may contribute to the mechanisms underlying insulin sensitivity and several metabolic disorders.
- Published
- 2013
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- View/download PDF
46. Barrier abnormality due to ceramide deficiency leads to psoriasiform inflammation in a mouse model.
- Author
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Nakajima K, Terao M, Takaishi M, Kataoka S, Goto-Inoue N, Setou M, Horie K, Sakamoto F, Ito M, Azukizawa H, Kitaba S, Murota H, Itami S, Katayama I, Takeda J, and Sano S
- Subjects
- Animals, Dermatitis immunology, Dermatitis pathology, Disease Models, Animal, Epidermis pathology, Female, Humans, Interleukin-17 metabolism, Interleukin-23 genetics, Interleukin-23 metabolism, Interleukins genetics, Interleukins metabolism, Keratinocytes metabolism, Keratinocytes pathology, Langerhans Cells immunology, Langerhans Cells metabolism, Langerhans Cells pathology, Male, Mice, Mice, Knockout, Psoriasis immunology, Psoriasis pathology, Serine C-Palmitoyltransferase metabolism, T-Lymphocytes immunology, T-Lymphocytes metabolism, T-Lymphocytes pathology, Water metabolism, Interleukin-22, Ceramides deficiency, Dermatitis metabolism, Epidermis metabolism, Psoriasis metabolism, Serine C-Palmitoyltransferase genetics
- Abstract
It has been recognized that ceramides are decreased in the epidermis of patients with psoriasis and atopic dermatitis. Here, we generated Sptlc2 (serine palmitoyltransferase long-chain base subunit 2)-targeted mice (SPT-cKO mice), thereby knocking out serine palmitoyltransferase (SPT), the critical enzyme for ceramide biosynthesis, in keratinocytes. SPT-cKO mice showed decreased ceramide levels in the epidermis, which impaired water-holding capacity and barrier function. From 2 weeks of age, they developed skin lesions with histological aberrations including hyperkeratosis, acanthosis, loss of the granular layer, and inflammatory cell infiltrates. Epidermal Langerhans cells showed persistent activation and enhanced migration to lymph nodes. Skin lesions showed upregulation of psoriasis-associated genes, such as IL-17A, IL-17F, IL-22, S100A8, S100A9, and β-defensins. In the skin lesions and draining lymph nodes, there were increased numbers of γδ T cells that produced IL-17 (γδ-17 cells), most of which also produced IL-22, as do Th17 cells. Furthermore, IL-23-producing CD11c(+) cells were observed in the lesions. In vivo treatment of SPT-cKO mice with an anti-IL-12/23p40 antibody ameliorated the skin lesions and reduced the numbers of γδ-17 cells. Therefore, we conclude that a ceramide deficiency in the epidermis leads to psoriasis-like lesions in mice, probably mediated by IL-23-dependent IL-22-producing γδ-17 cells.
- Published
- 2013
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47. Expression of human Gaucher disease gene GBA generates neurodevelopmental defects and ER stress in Drosophila eye.
- Author
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Suzuki T, Shimoda M, Ito K, Hanai S, Aizawa H, Kato T, Kawasaki K, Yamaguchi T, Ryoo HD, Goto-Inoue N, Setou M, Tsuji S, and Ishida N
- Subjects
- Amino Acid Sequence, Animals, Animals, Genetically Modified, Blotting, Western, Cells, Cultured, Developmental Disabilities pathology, Disease Models, Animal, Drosophila melanogaster genetics, Drosophila melanogaster metabolism, Endoplasmic Reticulum Stress, Eye growth & development, Eye metabolism, Glucosylceramidase metabolism, Humans, Molecular Sequence Data, Nervous System metabolism, RNA, Messenger genetics, Real-Time Polymerase Chain Reaction, Reverse Transcriptase Polymerase Chain Reaction, Developmental Disabilities genetics, Drosophila melanogaster growth & development, Eye embryology, Gaucher Disease pathology, Glucosylceramidase genetics, Mutation genetics, Nervous System pathology
- Abstract
Gaucher disease (GD) is the most common of the lysosomal storage disorders and is caused by defects in the GBA gene encoding glucocerebrosidase (GlcCerase). The accumulation of its substrate, glucocylceramide (GlcCer) is considered the main cause of GD. We found here that the expression of human mutated GlcCerase gene (hGBA) that is associated with neuronopathy in GD patients causes neurodevelopmental defects in Drosophila eyes. The data indicate that endoplasmic reticulum (ER) stress was elevated in Drosophila eye carrying mutated hGBAs by using of the ER stress markers dXBP1 and dBiP. We also found that Ambroxol, a potential pharmacological chaperone for mutated hGBAs, can alleviate the neuronopathic phenotype through reducing ER stress. We demonstrate a novel mechanism of neurodevelopmental defects mediated by ER stress through expression of mutants of human GBA gene in the eye of Drosophila.
- Published
- 2013
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48. Lysophosphatidylcholine acyltransferase 1 altered phospholipid composition and regulated hepatoma progression.
- Author
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Morita Y, Sakaguchi T, Ikegami K, Goto-Inoue N, Hayasaka T, Hang VT, Tanaka H, Harada T, Shibasaki Y, Suzuki A, Fukumoto K, Inaba K, Murakami M, Setou M, and Konno H
- Subjects
- 1-Acylglycerophosphocholine O-Acyltransferase antagonists & inhibitors, 1-Acylglycerophosphocholine O-Acyltransferase genetics, Aged, Aged, 80 and over, Carcinoma, Hepatocellular genetics, Carcinoma, Hepatocellular pathology, Cell Line, Tumor, Cell Movement, Cell Proliferation, Disease Progression, Female, Gene Knockdown Techniques, Hep G2 Cells, Humans, Liver Neoplasms genetics, Liver Neoplasms pathology, Male, Middle Aged, Neoplasm Invasiveness, Phospholipids chemistry, RNA, Messenger genetics, RNA, Messenger metabolism, RNA, Neoplasm genetics, RNA, Neoplasm metabolism, Substrate Specificity, Up-Regulation, 1-Acylglycerophosphocholine O-Acyltransferase metabolism, Carcinoma, Hepatocellular metabolism, Liver Neoplasms metabolism, Phospholipids metabolism
- Abstract
Background & Aims: Several lipid synthesis pathways play important roles in the development and progression of hepatocellular carcinoma (HCC), although the precise molecular mechanisms remain to be elucidated. Here, we show the relationship between HCC progression and alteration of phospholipid composition regulated by lysophosphatidylcholine acyltransferase (LPCAT)., Methods: Molecular lipidomic screening was performed by imaging mass spectrometry (IMS) in 37 resected HCC specimens. RT-PCR and Western blotting were carried out to examine the mRNA and protein levels of LPCATs, which catalyze the conversion of lysophosphatidylcholine (LPC) into phosphatidylcholine (PC) and have substrate specificity for some kinds of fatty acids. We examined the effect of LPCAT1 overexpression or knockdown on cell proliferation, migration, and invasion in HCC cell lines., Results: IMS revealed the increase of PC species with palmitoleic acid or oleic acid at the sn-2-position and the reduction of LPC with palmitic acid at the sn-1-position in HCC tissues. mRNA and protein of LPCAT1, responsible for LPC to PC conversion, were more abundant in HCCs than in the surrounding parenchyma. In cell line experiments, LPCAT1 overexpression enriched PCs observed in IMS and promoted cell proliferation, migration, and invasion. LPCAT1 knockdown did viceversa., Conclusions: Enrichment or depletion of some specific PCs, was found in HCC by IMS. Alteration of phospholipid composition in HCC would affect tumor character. LPCAT1 modulates phospholipid composition to create favorable conditions to HCC cells. LPCAT1 is a potent target molecule to inhibit HCC progression., (Copyright © 2013 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.)
- Published
- 2013
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49. Adventitial vasa vasorum arteriosclerosis in abdominal aortic aneurysm.
- Author
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Tanaka H, Zaima N, Sasaki T, Hayasaka T, Goto-Inoue N, Onoue K, Ikegami K, Morita Y, Yamamoto N, Mano Y, Sano M, Saito T, Sato K, Konno H, Setou M, and Unno N
- Subjects
- Aged, Aged, 80 and over, Female, Heme metabolism, Humans, Immunohistochemistry, Lipids chemistry, Male, Middle Aged, Adventitia pathology, Aortic Aneurysm, Abdominal complications, Aortic Aneurysm, Abdominal pathology, Arteriosclerosis complications, Arteriosclerosis pathology, Vasa Vasorum pathology
- Abstract
Abdominal aortic aneurysm (AAA) is a common disease among elderly individuals. However, the precise pathophysiology of AAA remains unknown. In AAA, an intraluminal thrombus prevents luminal perfusion of oxygen, allowing only the adventitial vaso vasorum (VV) to deliver oxygen and nutrients to the aortic wall. In this study, we examined changes in the adventitial VV wall in AAA to clarify the histopathological mechanisms underlying AAA. We found marked intimal hyperplasia of the adventitial VV in the AAA sac; further, immunohistological studies revealed proliferation of smooth muscle cells, which caused luminal stenosis of the VV. We also found decreased HemeB signals in the aortic wall of the sac as compared with those in the aortic wall of the neck region in AAA. The stenosis of adventitial VV in the AAA sac and the malperfusion of the aortic wall observed in the present study are new aspects of AAA pathology that are expected to enhance our understanding of this disease.
- Published
- 2013
- Full Text
- View/download PDF
50. GPHR-dependent functions of the Golgi apparatus are essential for the formation of lamellar granules and the skin barrier.
- Author
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Tarutani M, Nakajima K, Uchida Y, Takaishi M, Goto-Inoue N, Ikawa M, Setou M, Kinoshita T, Elias PM, Sano S, and Maeda Y
- Subjects
- Animals, Antimicrobial Cationic Peptides, Cathelicidins metabolism, Cell Differentiation, Inflammation, Ion Channels chemistry, Kallikreins metabolism, Keratinocytes cytology, Membrane Glycoproteins metabolism, Mice, Mice, Knockout, Models, Biological, Models, Genetic, Golgi Apparatus metabolism, Skin metabolism
- Abstract
The lumen of the Golgi apparatus is regulated to be weakly acidic, which is critical for its functions. The Golgi pH regulator (GPHR) is an anion channel essential for normal acidification of the Golgi apparatus, and is therefore required for its functions. The Golgi apparatus has been thought to be the origin of lamellar granules in the skin. To study the functional role(s) of GPHR in the skin, we established keratinocyte-specific GPHR-knockout mice using the Cre-loxP system. These mutant mice exhibited hypopigmented skin, hair loss, and scaliness. Histological examination of GPHR-knockout mice showed ballooning of the basal cells and follicular dysplasia. In addition, inflammatory cells were seen in the dermis. The expression of trans-Golgi network 46, a marker for lamellar bodies, and kallikrein 7, a protein within lamellar bodies, is diminished in GPHR-knockout mouse skin. Examination by electron microscopy revealed that keratinocytes produced aberrant lamellar bodies. The transepidermal water loss of these knockout mice was increased compared with wild-type mice. Moreover, expression of cathelicidin-related antimicrobial peptide (CRAMP) in the skin was diminished. These results suggest that GPHR is essential for the homeostasis of the epidermis including the formation of lamellar bodies and for the barrier function.
- Published
- 2012
- Full Text
- View/download PDF
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