19 results on '"Moritoh, Satoru"'
Search Results
2. DNA methylation is reconfigured at the onset of reproduction in rice shoot apical meristem
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Higo, Asuka, Saihara, Noriko, Miura, Fumihito, Higashi, Yoko, Yamada, Megumi, Tamaki, Shojiro, Ito, Tasuku, Tarutani, Yoshiaki, Sakamoto, Tomoaki, Fujiwara, Masayuki, Kurata, Tetsuya, Fukao, Yoichiro, Moritoh, Satoru, Terada, Rie, Kinoshita, Toshinori, Ito, Takashi, Kakutani, Tetsuji, Shimamoto, Ko, and Tsuji, Hiroyuki
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- 2020
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3. Involvement of the mitochondrial protein translocator component tim50 in growth, cell proliferation and the modulation of respiration in Drosophila
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Sugiyama, Shin, Moritoh, Satoru, Furukawa, Yoshimi, Mizuno, Tomohiko, Lim, Young-Mi, Tsuda, Leo, and Nishida, Yasuyoshi
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Drosophila -- Physiological aspects ,Drosophila -- Growth ,Drosophila -- Genetic aspects ,Mitochondria -- Chemical properties ,Mitochondria -- Genetic aspects ,Mitochondrial membranes -- Chemical properties ,Membrane proteins -- Physiological aspects ,Biological control systems -- Chemical properties ,Company growth ,Biological sciences - Abstract
Allelic mutants exhibiting growth defects in Drosophila were isolated. Molecular cloning identified the responsible gene as a budding yeast Tim50 ortholog, and thus it was named tiny tim 50 (ttm50). The weak allele ([ttm50.sup.Gp99]) produced small flies due to reduced cell size and number, and growth terminated at the larval stage in the strong alleles ([ttm50.sup.IE1] and [ttm50.sup.IE2]). Twin-spot analysis showed fewer cells in [ttm50.sup.Gp99] clones, whereas [ttm50.sup.IE1] clones did not proliferate, suggesting that the gene has an essential cellular function. Tim50 is known to maintain mitochondrial membrane potential (MMP) while facilitating innermembrane protein transport. We found that tagged Ttm50 also localized to mitochondria and that mitochondrial morphology and MMP were affected in mutants, indicating that mitochondrial dysfunction causes the developmental phenotype. Conversely, ttm50 overexpression increased MMP and apoptosis. Co-expression of p35 suppressed this apoptosis, resulting in cell overproliferation. Interestingly, ttm50 transcription was tissue specific, corresponding to elevated MMP in the larval midgut, which was decreased in the mutant. The correlation of ttm50 expression levels with differences in MMP match its proposed role in mitochondrial permeability barrier maintenance. Thus a mitochondrial protein translocase component can play active roles in regulating metabolic levels, possibly for modulation of physiological function or growth in development.
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- 2007
4. Targeted disruption of an orthologue of DOMAINS REARRANGED METHYLASE 2, OsDRM2, impairs the growth of rice plants by abnormal DNA methylation
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Moritoh, Satoru, Eun, Chang-Ho, Ono, Akemi, Asao, Hisayo, Okano, Yosuke, Yamaguchi, Katsushi, Shimatani, Zenpei, Koizumi, Amane, and Terada, Rie
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- 2012
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5. RNAi-mediated Silencing of OsGEN-L (OsGEN-like), a New Member of the RAD2/XPG Nuclease Family, Causes Male Sterility by Defect of Microspore Development in Rice
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Moritoh, Satoru, Miki, Daisuke, Akiyama, Masahiro, Kawahara, Mihoko, Izawa, Takeshi, Maki, Hisaji, and Shimamoto, Ko
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- 2005
6. Endogenous arginine vasopressin–positive retinal cells in arginine vasopressin–eGFP transgenic rats identified by immunohistochemistry and reverse transcriptase–polymerase chain reaction
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Moritoh, Satoru, Sato, Kaori, Okada, Yasunobu, and Koizumi, Amane
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Male ,Retinal Ganglion Cells ,endocrine system ,Receptors, Vasopressin ,urogenital system ,Reverse Transcriptase Polymerase Chain Reaction ,Green Fluorescent Proteins ,Gene Expression ,Immunohistochemistry ,Rats ,Arginine Vasopressin ,nervous system ,Paracrine Communication ,Animals ,Vasoconstrictor Agents ,sense organs ,RNA, Messenger ,Rats, Transgenic ,Rats, Wistar ,hormones, hormone substitutes, and hormone antagonists ,Research Article - Abstract
Purpose Recently, arginine vasopressin (AVP) has been revealed to have diverse functional roles in nervous tissues beyond that of a vasoconstrictor. Several previous studies have indicated the existence of AVP in the retina, but the source of AVP has not been determined. The objective of the present study was to address the question of whether retinal cells have the ability to synthesize endogenous AVP to act in a paracrine or autocrine manner. Methods We used AVP-eGFP transgenic rats to find endogenous AVP-positive cells in the retina by immunohistochemistry with an AVP antibody and a GFP antibody. We also examined AVP mRNA and AVP receptor genes by reverse transcriptase (RT)–PCR of dissociated GFP-positive cells and whole retinas. Results Endogenous AVP-positive cells were found in the ganglion cell layer and inner nuclear layer of the retina of AVP-eGFP transgenic rats by immunohistochemistry. As indicated by the results of RT–PCR of dissociated GFP-positive cells, these cells have the ability to synthesize endogenous AVP, as well as transgenic AVP-eGFP. In addition, the V1a and V1b AVP receptors were found in the wild-type rat retina by whole retina RT–PCR, but the V2 receptor was not detectable. In dissociated AVP-eGFP-positive cells, no AVP receptor was detected by RT–PCR. Moreover, AVP secretion was not detected by stimulation with a high potassium (50 mM) solution. Conclusions In the rat retina, we found retinal cells that have the ability to synthesize endogenous AVP, and that the retina possesses V1a and V1b AVP receptors. Taken together, these results suggest that the retina has an intrinsic AVP-synthesizing and -receiving mechanism that can operate in a paracrine manner via V1a and V1b receptors.
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- 2011
7. Different Activity Patterns in Retinal Ganglion Cells of TRPM1 and mGluR6 Knockout Mice.
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Takeuchi, Haruki, Horie, Sho, Moritoh, Satoru, Matsushima, Hiroki, Hori, Tesshu, Kimori, Yoshitaka, Kitano, Katsunori, Tsubo, Yasuhiro, Tachibana, Masao, and Koike, Chieko
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PHOTORECEPTORS ,RETINA physiology ,CELL receptors ,RETINAL ganglion cells ,ANIMAL experimentation ,BODY surface mapping ,CELLULAR signal transduction ,GLYCOPROTEINS ,MICE ,GENETIC mutation ,NEUROPHYSIOLOGY ,PHYSIOLOGY ,CELL physiology - Abstract
TRPM1, the first member of the melanoma-related transient receptor potential (TRPM) subfamily, is the visual transduction channel downstream of metabotropic glutamate receptor 6 (mGluR6) on retinal ON bipolar cells (BCs). Human TRPM1 mutations are associated with congenital stationary night blindness (CSNB). In both TRPM1 and mGluR6 KO mouse retinas, OFF but not ON BCs respond to light stimulation. Here we report an unexpected difference between TRPM1 knockout (KO) and mGluR6 KO mouse retinas. We used a multielectrode array (MEA) to record spiking in retinal ganglion cells (RGCs). We found spontaneous oscillations in TRPM1 KO retinas, but not in mGluR6 KO retinas. We performed a structural analysis on the synaptic terminals of rod ON BCs. Intriguingly, rod ON BC terminals were significantly smaller in TRPM1 KO retinas than in mGluR6 KO retinas. These data suggest that a deficiency of TRPM1, but not of mGluR6, in rod ON bipolar cells may affect synaptic terminal maturation. We speculate that impaired signaling between rod BCs and AII amacrine cells (ACs) leads to spontaneous oscillations. TRPM1 and mGluR6 are both essential components in the signaling pathway from photoreceptors to ON BC dendrites, yet they differ in their effects on the BC terminal and postsynaptic circuitry. [ABSTRACT FROM AUTHOR]
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- 2018
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8. Diversity of Retinal Ganglion Cells Identified by Transient GFP Transfection in Organotypic Tissue Culture of Adult Marmoset Monkey Retina.
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Moritoh, Satoru, Komatsu, Yusuke, Yamamori, Tetsuo, Koizumi, Amane, and Chuan-Chin Chiao
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RETINAL ganglion cells , *SENSORY ganglia , *GREEN fluorescent protein , *FLUORESCENT polymers , *GENE transfection , *TISSUE culture , *MARMOSETS - Abstract
The mammalian retina has more diversity of neurons than scientists had once believed in order to establish complicated vision processing. In the monkey retina, morphological diversity of retinal ganglion cells (RGCs) besides dominant midget and parasol cells has been suggested. However, characteristic subtypes of RGCs in other species such as bistratified direction-selective ganglion cells (DSGC) have not yet been identified. Increasing interest has been shown in the common marmoset (Callithrix jacchus) monkey as a "super-model" of neuroscientific research. Here, we established organotypic tissue culture of the adult marmoset monkey retina with particle-mediated gene transfer of GFP to survey the morphological diversity of RGCs. We successfully incubated adult marmoset monkey retinas for 2 to 4 days ex vivo for transient expression of GFP. We morphologically examined 121 RGCs out of more than 3240 GFP-transfected cells in 5 retinas. Among them, we identified monostratified or broadly stratified ganglion cells (midget, parasol, sparse, recursive, thorny, and broad thorny ganglion cells), and bistratified ganglion cells (recursive, large, and small bistratified ganglion cells [blue-ON/yellow-OFF-like]). By this survey, we also found a candidate for bistratified DSGC whose dendrites were well cofasciculated with ChAT-positive starburst dendrites, costratified with ON and OFF ChAT bands, and had honeycomb- shaped dendritic arbors morphologically similar to those in rabbits. Our genetic engineering method provides a new approach to future investigation for morphological and functional diversity of RGCs in the monkey retina. [ABSTRACT FROM AUTHOR]
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- 2013
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9. Organotypic Tissue Culture of Adult Rodent Retina Followed by Particle-Mediated Acute Gene Transfer In Vitro.
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Moritoh, Satoru, Tanaka, Kenji F., Hiroshi Jouhou, Ikenaka, Kazuhiro, and Koizumi, Amane
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RODENTS , *RETINA , *ORGAN culture , *CULTURES (Biology) , *BIOMOLECULES , *GENETIC transformation , *TISSUES - Abstract
Background: Organotypic tissue culture of adult rodent retina with an acute gene transfer that enables the efficient introduction of variable transgenes would greatly facilitate studies into retinas of adult rodents as animal models. However, it has been a difficult challenge to culture adult rodent retina. The purpose of this present study was to develop organotypic tissue culture of adult rodent retina followed by particle-mediated acute gene transfer in vitro. Methodology/Principal Findings: We established an interphase organotypic tissue culture for adult rat retinas (>P35 of age) which was optimized from that used for adult rabbit retinas. We implemented three optimizations: a greater volume of Ames' medium (>26 mL) per retina, a higher speed (constant 55 rpm) of agitation by rotary shaker, and a greater concentration (10%) of horse serum in the medium. We also successfully applied this method to adult mouse retina (>P35 of age). The organotypic tissue culture allowed us to keep adult rodent retina morphologically and structurally intact for at least 4 days. However, mouse retinas showed less viability after 4-day culture. Electrophysiologically, ganglion cells in cultured rat retina were able to generate action potentials, but exhibited less reliable light responses. After transfection of EGFP plasmids by particle-mediated acute gene transfer, we observed EGFP-expressing retinal ganglion cells as early as 1 day of culture. We also introduced polarized-targeting fusion proteins such as PSD95-GFP and melanopsin-EYFP (hOPN4-EYFP) into rat retinal ganglion cells. These fusion proteins were successfully transferred into appropriate locations on individual retinal neurons. Conclusions/Significance: This organotypic culture method is largely applicable to rat retinas, but it can be also applied to mouse retinas with a caveat regarding cell viability. This method is quite flexible for use in acute gene transfection in adult rodent retina, replacing molecular biological bioassays that used to be conducted in isolated cultured cells. [ABSTRACT FROM AUTHOR]
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- 2010
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10. Alternative splicing of the rice OsMET1 genes encoding maintenance DNA methyltransferase
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Yamauchi, Takaki, Moritoh, Satoru, Johzuka-Hisatomi, Yasuyo, Ono, Akemi, Terada, Rie, Nakamura, Ikuo, and Iida, Shigeru
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METHYLTRANSFERASES , *POLYMERASE chain reaction , *DNA polymerases , *ARABIDOPSIS - Abstract
Summary: While the Arabidopsis genome carries one copy of the methyltransferase 1 (MET1) gene for DNA methyltransferase, which is mainly responsible for maintaining CpG methylation, the rice genome bears two copies of the MET1 genes, OsMET1a and OsMET1b. The transcripts of OsMET1b accumulate more abundantly than those of OsMET1a in all of the tissues examined, and both genes actively transcribed at the callus, imbibed embryo, root, meristem, young panicle, anther, pistil, and endosperm, all of which contain actively dividing cells. The OsMET1a transcripts contain two 5′-untranslated exons and alternatively spliced 3′-terminal exons. The alternatively spliced transcripts consist of 14, 15, or 16 exons, and all of them encode a putative protein of 1527 amino acids. While the 3′-terminal exon of OsMET1b is unique, alternative splicing occurs in the 5′-terminal regions, which comprise either exons containing 5′-untranslated regions or an exon bearing the initiation codon. Depending upon alternative usage of 5′ exons by alternative splicing, the OsMET1b transcripts comprise 11, 12, 13, or 14 exons, and the former two and the latter two longer transcripts encode putative proteins of 1486 and 1529 amino acids, respectively. Moreover, the 5′ splicing patterns of OsMET1b can vary in different tissues. These findings are discussed with respect to the possible regulation of the OsMET1 genes. [Copyright &y& Elsevier]
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- 2008
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11. RNAi-mediated Silencing of <it>OsGEN-L</it> (<it>OsGEN-like</it>), a New Member of the RAD2/XPG Nuclease Family, Causes Male Sterility by Defect of Microspore Development in Rice.
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Moritoh, Satoru, Miki, Daisuke, Akiyama, Masahiro, Kawahara, Mihoko, Izawa, Takeshi, Maki, Hisaji, and Shimamoto, Ko
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PLANTS , *GREEN fluorescent protein , *PHYLOGENY , *NUCLEASES , *DNA , *MICROSPOREA , *RICE , *TRANSGENIC organisms - Abstract
We have cloned a new member of the RAD2/XPG nuclease family, OsGEN-L (OsGEN-like), from rice (Oryza sativa L.). OsGEN-L possesses two domains, the N- and I-regions, that are conserved in the RAD2/XPG nuclease family. Database searches and phylogenetic analyses revealed that OsGEN-L belongs to class 4 of the RAD2/XPG nuclease family, and OsGEN-L homologs were found in animals and higher plants. To elucidate the function of OsGEN-L, we generated rice OsGEN-L-RNAi transgenic plants in which OsGEN-L expression was silenced. Most of the OsGEN-L-RNAi plants displayed low fertility, and some of them were male-sterile. OsGEN-L-RNAi plants lacked mature pollen, resulting from a defect in early microspore development. A OsGEN-L–green fluorescent protein (GFP) fusion protein was localized in the nucleus, and the OsGEN-L promoter was specifically active in the anthers. Furthermore, a recombinant OsGEN-L protein possessed flap endonuclease activity and both single-stranded and double-stranded DNA-binding activities. Our results suggest that OsGEN-L plays an essential role in DNA metabolism required for early microspore development in rice. [ABSTRACT FROM AUTHOR]
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- 2005
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12. Organotypic culture of adult rodent retina with particle-mediated acute gene transfer in vitro
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Moritoh, Satoru, Tanaka, Kenji F., Ikenaka, Kazuhiro, and Koizumi, Amane
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- 2010
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13. Gene delivery to cone photoreceptors by subretinal injection of rAAV2/6 in the mouse retina.
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Hori, Tesshu, Fukutome, Masashi, Maejima, Chiseto, Matsushima, Hiroki, Kobayashi, Kensuke, Kitazawa, Soichiro, Kitahara, Ryo, Kitano, Katsunori, Kobayashi, Kenta, Moritoh, Satoru, and Koike, Chieko
- Abstract
Adeno-associated virus (AAV) has been studied as a safe delivery tool for gene therapy of retinal blinding diseases such as Leber's congenital amaurosis (LCA). The tropism of recombinant AAV (rAAV) including its specificity and efficiency in targeting retinal cell types has been studied with native or engineered capsids, along with specific promoters. However, one of the rAAV serotypes, rAAV2/6, has not been well-studied based on a report of low infection efficiency in the retina. We investigated the tropism of several rAAVs by subretinal injection in the adult mouse and found that rAAV2/6 predominantly infected cone photoreceptors including the main spectral type. Our data suggest that subretinal injection with rAAV2/6 may provide both an efficacious and specific means of gene delivery to cone photoreceptors in murine retinas. Image 1 • Cone photoreceptors are targets for gene therapy for diseases such as mid-stage retinitis pigmentosa and achromatopsia. • rAAV has been considered as an effective and safe delivery tool for gene therapy in the retina. • The tropism of rAAV2/6 has been studied in the retina but not in detail. • We show that subretinally injected rAAV2/6 predominantly infects cone photoreceptors as opposed to rods. • Our results suggest that AAV2/6 may be an appropriate vector for introducing therapeutic genes into cones. [ABSTRACT FROM AUTHOR]
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- 2019
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14. Optogenetic stimulus-triggered acquisition of seizure resistance.
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Shimoda, Yoshiteru, Beppu, Kaoru, Ikoma, Yoko, Morizawa, Yosuke M., Zuguchi, Satoshi, Hino, Utaro, Yano, Ryutaro, Sugiura, Yuki, Moritoh, Satoru, Fukazawa, Yugo, Suematsu, Makoto, Mushiake, Hajime, Nakasato, Nobukazu, Iwasaki, Masaki, Tanaka, Kenji F., Tominaga, Teiji, and Matsui, Ko
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BRAIN stimulation , *SEIZURES (Medicine) , *ENGINEERING plastics , *ELECTRIC stimulation , *PLASTICS engineering - Abstract
Unlike an electrical circuit, the hardware of the brain is susceptible to change. Repeated electrical brain stimulation mimics epileptogenesis. After such "kindling" process, a moderate stimulus would become sufficient in triggering a severe seizure. Here, we report that optogenetic neuronal stimulation can also convert the rat brain to a hyperexcitable state. However, continued stimulation once again converted the brain to a state that was strongly resistant to seizure induction. Histochemical examinations showed that moderate astrocyte activation was coincident with resilience acquisition. Administration of an adenosine A1 receptor antagonist instantly reverted the brain back to a hyperexcitable state, suggesting that hyperexcitability was suppressed by adenosine. Furthermore, an increase in basal adenosine was confirmed using in vivo microdialysis. Daily neuron-to-astrocyte signaling likely prompted a homeostatic increase in the endogenous actions of adenosine. Our data suggest that a certain stimulation paradigm could convert the brain circuit resilient to epilepsy without exogenous drug administration. • Functional engineering and plastic conversion of the brain state were attempted. • Optogenetic neuronal stimulation succeeded in creating a seizure-resistant brain. • Daily neuron-to-astrocyte signaling likely prompted endogenous adenosine release. • Homeostasis of the brain has the potential of local containment of hyperexcitation. [ABSTRACT FROM AUTHOR]
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- 2022
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15. Bilberry extract administration prevents retinal ganglion cell death in mice via the regulation of chaperone molecules under conditions of endoplasmic reticulum stress.
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Nakamura O, Moritoh S, Sato K, Maekawa S, Murayama N, Himori N, Omodaka K, Sogon T, and Nakazawa T
- Abstract
Purpose: To investigate the effect of bilberry extract anthocyanins on retinal ganglion cell (RGC) survival after optic nerve crush. Additionally, to determine details of the mechanism of the neuroprotective effect of bilberry extract anthocyanins and the involvement of endoplasmic reticulum stress suppression in the mouse retina., Materials and Methods: Anthocyanins in bilberry extract (100 mg/kg/day or 500 mg/kg/day) were administrated orally to C57BL/6J mice. The expression levels of various molecular chaperones were assessed with quantitative reverse-transcription polymerase chain reaction, Western blotting, and immunohistochemistry. RGC survival was evaluated by measuring the gene expression of RGC markers and counting retrogradely labeled RGCs after optic nerve crush., Results: The protein levels of Grp78 and Grp94 increased significantly in mice after bilberry extract administration. Increased Grp78 and Grp94 levels were detected in the inner nuclear layer and ganglion cell layer of the retina, surrounding the RGCs. Gene expression of Chop , Bax , and Atf4 increased in mice after optic nerve crush and decreased significantly after oral bilberry extract administration. RGC survival after nerve crush also increased with bilberry extract administration., Conclusion: These results indicate that oral bilberry extract administration suppresses RGC death. Bilberry extract administration increased Grp78 and Grp94 protein levels, an effect which may underlie the neuroprotective effect of bilberry extract after optic nerve crush. Thus, bilberry extract has a potential role in neuroprotective treatments for retinal injuries, such as those which occur in glaucoma., Competing Interests: Disclosure This work was funded by Wakasa Seikatsu Co. Ltd. (T Sogon is an employee). The authors report no other conflicts of interest in this work.
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- 2017
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16. The neuroprotective effect of hesperidin in NMDA-induced retinal injury acts by suppressing oxidative stress and excessive calpain activation.
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Maekawa S, Sato K, Fujita K, Daigaku R, Tawarayama H, Murayama N, Moritoh S, Yabana T, Shiga Y, Omodaka K, Maruyama K, Nishiguchi KM, and Nakazawa T
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- Animals, Apoptosis drug effects, Cells, Cultured, Disease Models, Animal, Evoked Potentials, Visual drug effects, Hesperidin pharmacology, Male, Mice, Neuroprotective Agents pharmacology, Oxidative Stress drug effects, Retina cytology, Retina drug effects, Retina metabolism, Retinal Diseases chemically induced, Retinal Diseases genetics, Retinal Diseases metabolism, Retinal Ganglion Cells drug effects, Retinal Ganglion Cells metabolism, Treatment Outcome, Tumor Necrosis Factor-alpha genetics, Calpain metabolism, Hesperidin administration & dosage, N-Methylaspartate adverse effects, Neuroprotective Agents administration & dosage, Retinal Diseases drug therapy, Retinal Ganglion Cells cytology
- Abstract
We found that hesperidin, a plant-derived bioflavonoid, may be a candidate agent for neuroprotective treatment in the retina, after screening 41 materials for anti-oxidative properties in a primary retinal cell culture under oxidative stress. We found that the intravitreal injection of hesperidin in mice prevented reductions in markers of the retinal ganglion cells (RGCs) and RGC death after N-methyl-D-aspartate (NMDA)-induced excitotoxicity. Hesperidin treatment also reduced calpain activation, reactive oxygen species generation and TNF-α gene expression. Finally, hesperidin treatment improved electrophysiological function, measured with visual evoked potential, and visual function, measured with optomotry. Thus, we found that hesperidin suppressed a number of cytotoxic factors associated with NMDA-induced cell death signaling, such as oxidative stress, over-activation of calpain, and inflammation, thereby protecting the RGCs in mice. Therefore, hesperidin may have potential as a therapeutic supplement for protecting the retina against the damage associated with excitotoxic injury, such as occurs in glaucoma and diabetic retinopathy.
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- 2017
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17. Topical ocular dexamethasone decreases intraocular pressure and body weight in rats.
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Sato K, Nishiguchi KM, Maruyama K, Moritoh S, Fujita K, Ikuta Y, Kasai H, and Nakazawa T
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- Administration, Ophthalmic, Alanine Transaminase blood, Animals, Biomarkers, Blood Glucose analysis, Cholesterol blood, Dexamethasone therapeutic use, Endoplasmic Reticulum Stress, Male, Mice, Rats, Sprague-Dawley, Body Weight drug effects, Dexamethasone pharmacology, Intraocular Pressure drug effects, Ocular Hypertension drug therapy
- Abstract
Background: Recently, topical dexamethasone-induced ocular hypertension and a consequent loss of retinal ganglion cells (RGCs) have been described in mice. This has been proposed as a model of steroid-induced glaucoma. In this study, we set up and evaluated a similar model in rats., Results: Ten-week old Sprague Dawley (SD) rats (N = 12) were used to evaluate the effect of topical 0.1% dexamethasone (50 μl) administered 3 times daily for 4 weeks. Sodium chloride (0.9%) was used in another group of rats (N = 12) that served as the controls. After 1 week, we observed a progressive decrease in body weight in the dexamethasone-treated rats compared both to the pre-treatment baseline and the vehicle-treated rats. In contrast to earlier work that showed elevated Intraocular pressure (IOP) following dexamethasone instillation in mice, IOP in the rats unexpectedly fell to 11.3 ± 1.3 mmHg in the treated eyes, compared to 14.8 ± 2.4 mmHg in the untreated eyes, after 3 weeks of topical dexamethasone (P = 0.032). Blood tests performed after 4 weeks of treatment showed a 3.3-fold increase in both plasma cholesterol (P < 0.001) and alanine transaminase (P = 0.019) in the dexamethasone-treated rats compared to the control rats. Meanwhile, topical steroid did not induce changes in either plasma blood glucose or glycated hemoglobin (HbA1c). We also did not detect changes in the expression of RGC markers (with real-time PCR) following the treatment., Conclusions: In contrast to mice, which previously showed increased IOP following the topical administration of dexamethasone, the rats displayed a paradoxical reduction in IOP following a similar treatment. This was accompanied by a loss of body weight without affecting the level of blood glucose.
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- 2016
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18. In vivo visualization of subtle, transient, and local activity of astrocytes using an ultrasensitive Ca(2+) indicator.
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Kanemaru K, Sekiya H, Xu M, Satoh K, Kitajima N, Yoshida K, Okubo Y, Sasaki T, Moritoh S, Hasuwa H, Mimura M, Horikawa K, Matsui K, Nagai T, Iino M, and Tanaka KF
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- Animals, Calcium-Binding Proteins genetics, Fluorescence Resonance Energy Transfer, Mice, Somatosensory Cortex cytology, Astrocytes metabolism, Calcium Signaling, Calcium-Binding Proteins metabolism, Somatosensory Cortex metabolism
- Abstract
Astrocytes generate local calcium (Ca(2+)) signals that are thought to regulate their functions. Visualization of these signals in the intact brain requires an imaging method with high spatiotemporal resolution. Here, we describe such a method using transgenic mice expressing the ultrasensitive ratiometric Ca(2+) indicator yellow Cameleon-Nano 50 (YC-Nano50) in astrocytes. In these mice, we detected a unique pattern of Ca(2+) signals. These occur spontaneously, predominantly in astrocytic fine processes, but not the cell body. Upon sensory stimulation, astrocytes initially responded with Ca(2+) signals at fine processes, which then propagated to the cell body. These observations suggest that astrocytic fine processes function as a high-sensitivity detector of neuronal activities. Thus, the method provides a useful tool for studying the activity of astrocytes in brain physiology and pathology., (Copyright © 2014 The Authors. Published by Elsevier Inc. All rights reserved.)
- Published
- 2014
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19. The effect of podoplanin inhibition on lymphangiogenesis under pathological conditions.
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Maruyama Y, Maruyama K, Kato Y, Kajiya K, Moritoh S, Yamamoto K, Matsumoto Y, Sawane M, Kerjaschki D, Nakazawa T, and Kinoshita S
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- Animals, Blotting, Western, Cells, Cultured, Cornea drug effects, Cornea pathology, Corneal Neovascularization metabolism, Corneal Neovascularization pathology, Corneal Transplantation, Disease Models, Animal, Endothelium, Lymphatic drug effects, Endothelium, Lymphatic metabolism, Enzyme-Linked Immunosorbent Assay, Macrophages metabolism, Macrophages pathology, Male, Membrane Glycoproteins metabolism, Mice, Mice, Inbred BALB C, Mice, Inbred C57BL, Mitogen-Activated Protein Kinases metabolism, Tumor Necrosis Factor-alpha metabolism, Wound Healing drug effects, Cornea blood supply, Corneal Neovascularization prevention & control, Endothelium, Lymphatic pathology, Lymphangiogenesis drug effects, Membrane Glycoproteins antagonists & inhibitors
- Abstract
Purpose: Podoplanin has been shown to be a reliable marker of lymphatic endothelium, but its role in the lymphatic system has not been well investigated. The purpose of this study is to investigate the role of podoplanin in lymphangiogenesis and macrophage functions under inflammatory conditions., Methods: Mouse corneal suture and ear section models were used to induce lymphangiogenesis and macrophage infiltration. Antilymphatic vessel endothelial hyaluronan-1 (Anti-LYVE-1) antibody was used to visualize lymphatic vessels. Thioglycollate-induced macrophages (mps) were collected and cultured with lipopolysaccharide (LPS), IFN-γ, and anti-mouse podoplanin antibody (PMab-1). Podoplanin, NF-κB, and mitogen-activated protein kinase (MAPK) pathway expression were detected by Western blot analysis. The TNF-α secretion was measured by ELISA., Results: Administration of PMab-1, reduced lymphangiogenesis in the corneal suture and ear wound healing models. Also, PMab-1 suppressed mps infiltration at the site of wound healing. Moreover, administration of PMab-1 led to a significant suppression of the rejection reaction in the corneal transplantation model. Our in vitro experiments showed that PMab-1 suppressed TNF-α secretion from mps under inflamed conditions, especially secretion caused by LPS stimulation. We confirmed the effect of PMab-1 on mps under inflamed conditions with a Western blot experiment, which clearly showed that the phosphorylation signal of the MAPK and NF-κB pathways was suppressed by PMab-1., Conclusions: Podoplanin neutralization resulted in inhibition of lymphatic growth associated with corneal and ear wound healing as well as mps inflammation. These data suggest that podoplanin is a novel therapeutic target for suppressing lymphangiogenesis and inflammation., (Copyright 2014 The Association for Research in Vision and Ophthalmology, Inc.)
- Published
- 2014
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