14 results on '"Yandi Wu"'
Search Results
2. Retinol dehydrogenase 10 reduction mediated retinol metabolism disorder promotes diabetic cardiomyopathy in male mice
- Author
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Yandi Wu, Tongsheng Huang, Xinghui Li, Conghui Shen, Honglin Ren, Haiping Wang, Teng Wu, Xinlu Fu, Shijie Deng, Ziqi Feng, Shijie Xiong, Hui Li, Saifei Gao, Zhenyu Yang, Fei Gao, Lele Dong, Jianding Cheng, and Weibin Cai
- Subjects
Science - Abstract
The current challenges for diabetic cardiomyopathy (DCM) are unclear mechanisms and no effective therapy in clinics. Here, the authors found that the decrease of cardiac retinol dehydrogenase 10 in type 2 diabetes leads to retinol metabolism disorder, cardiac lipid toxicity and cardiomyopathy development, suggesting that correcting the imbalance of cardiac retinol metabolism may be an effective strategy for the treatment of DCM.
- Published
- 2023
- Full Text
- View/download PDF
3. Transcriptome analysis reveals pathogenesis-related gene 1 pathway against salicylic acid treatment in grapevine (Vitis vinifera L)
- Author
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Faiz Ur Rahman, Irshad Ahmad Khan, Ali Aslam, Ruitao Liu, Lei Sun, Yandi Wu, Muhammad Muzammal Aslam, Asad Ullah Khan, Peng Li, Jianfu Jiang, Xiucai Fan, Chonghuai Liu, and Ying Zhang
- Subjects
Salicylic acid ,PR1 ,white rot ,Cis-elements ,transcriptomics ,grapevine ,Genetics ,QH426-470 - Abstract
Salicylic acid (SA) is a well-studied phenolic plant hormone that plays an important role in plant defense against the hemi-biothrophic and biothrophic pathogens and depends on the living cells of host for the successful infection. In this study, a pathogenesis test was performed between Vitis davidii and V. vinifera cultivars against grape white rot disease (Coniella diplodiella). V. davidii was found to be resistant against this disease. SA contents were found to be higher in the resistant grape cultivar after different time points. RNA-seq analysis was conducted on susceptible grapevine cultivars after 12, 24, and 48 h of SA application with the hypothesis that SA may induce defense genes in susceptible cultivars. A total of 511 differentially expressed genes (DEGs) were identified from the RNA-seq data, including some important genes, VvWRKY1/2, VvNPR1, VvTGA2, and VvPR1, for the SA defense pathway. DEGs related to phytohormone signal transduction and flavonoid biosynthetic pathways were also upregulated. The quantitative real-time PCR (qRT-PCR) results of the significantly expressed transcripts were found to be consistent with the transcriptome data, with a high correlation between the two analyses. The pathogenesis-related gene 1 (VvPR1), which is an important marker gene for plant defense, was selected for further promoter analysis. The promoter sequence showed that it contains some important cis-elements (W-box, LS7, as-1, and TCA-element) to recruit the transcription factors VvWRKY, VvNPR1, and VvTGA2 to express the VvPR1 gene in response to SA treatment. Furthermore, the VvPR1 promoter was serially deleted into different fragments (−1,837, −1,443, −1,119, −864, −558, −436, and −192 ) bp and constructed vectors with the GUS reporter gene. Deletion analysis revealed that the VvPR1 promoter between −1837 bp to −558 bp induced significant GUS expression with respect to the control. On the basis of these results, the −558 bp region was assumed to be an important part of the VvPR1 promoter, and this region contained the important cis-elements related to SA, such as TCA-element (−1,472 bp), LS7 (−1,428 bp), and as-1 (−520 bp), that recruit the TFs and induce the expression of the VvPR1 gene. This study expanded the available information regarding SA-induced defense in susceptible grapes and recognized the molecular mechanisms through which this defense might be mediated.
- Published
- 2022
- Full Text
- View/download PDF
4. Moderate heart rate reduction promotes cardiac regeneration through stimulation of the metabolic pattern switch
- Author
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Jing Tan, Ming Yang, Haiping Wang, Conghui Shen, Maoxiong Wu, He Xu, Yandi Wu, Yuanlong Li, Xinghui Li, Tongsheng Huang, Shijie Deng, Zhenyu Yang, Saifei Gao, Hui Li, Jiaguo Zhou, Hui Chen, Nan Cao, and Weibin Cai
- Subjects
heart rate ,cardiomyocyte proliferation ,heart regeneration ,metabolic pattern ,metoprolol ,ivabradine ,Biology (General) ,QH301-705.5 - Abstract
Summary: As a biological pump, the heart needs to consume a substantial amount of energy to maintain sustained beating. Myocardial energy metabolism was recently reported to be related to the loss of proliferative capacity in cardiomyocytes (CMs). However, the intrinsic relationship between beating rate and proliferation in CMs and whether energy metabolism can regulate this relationship remains unclear. In this study, we find that moderate heart rate reduction (HRR) induces CM proliferation under physiological conditions and promotes cardiac regenerative repair after myocardial injury. Mechanistically, moderate HRR induces G1/S transition and increases the expression of glycolytic enzymes in CMs. Furthermore, moderate HRR induces a metabolic pattern switch, activating glucose metabolism and increasing the relative proportion of ATP production by the glycolytic pathway for biosynthesis of substrates needed for proliferative CMs. These results highlight the potential therapeutic role of HRR in not only acute myocardial protection but also long-term CM restoration.
- Published
- 2022
- Full Text
- View/download PDF
5. The Promoter Analysis of VvPR1 Gene: A Candidate Gene Identified through Transcriptional Profiling of Methyl Jasmonate Treated Grapevine (Vitis vinifera L.)
- Author
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Faiz Ur Rahman, Ying Zhang, Irshad Ahmad Khan, Ruitao Liu, Lei Sun, Yandi Wu, Jianfu Jiang, Xiucai Fan, and Chonghuai Liu
- Subjects
grape ,MeJA ,Transcriptome ,PR1 ,GUS ,β-glucuronidase ,Botany ,QK1-989 - Abstract
Methyl jasmonate (MeJA) plays a vital role in plant disease resistance and also induces the expression of disease resistance genes in plants. In this study, a transcriptome analysis was performed on grapevine leaves after 12, 24 and 48 h of MeJA-100 μM treatment. A total of 1242 differentially expressed genes (DEGs) were identified from the transcriptome data, and the analysis of the DEGs showed that genes related to phytohormone signal transduction, jasmonic acid-mediated defense, Mitogen-activated protein kinase (MAPK), and flavonoid biosynthetic pathways were upregulated. As Pathogenesis-related gene 1 (PR1) is an important marker gene in plant defense also upregulated by MeJA treatment in RNA-seq data, the VvPR1 gene was selected for a promoter analysis with β-glucuronidase (GUS) through transient expression in tobacco leaves against abiotic stress. The results showed that the region from −1837 bp to −558 bp of the VvPR1 promoter is the key region in response to hormone and wound stress. In this study, we extended the available knowledge about induced defense by MeJA in a grapevine species that is susceptible to different diseases and identified the molecular mechanisms by which this defense might be mediated.
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- 2022
- Full Text
- View/download PDF
6. Pigment Epithelial‐Derived Factor Deficiency Accelerates Atherosclerosis Development via Promoting Endothelial Fatty Acid Uptake in Mice With Hyperlipidemia
- Author
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Haiping Wang, Yanfang Yang, Ming Yang, Xinghui Li, Jing Tan, Yandi Wu, Yuling Zhang, Yuanlong Li, Bo Hu, Shijie Deng, Fengmin Yang, Saifei Gao, Hui Li, Zhenyu Yang, Hui Chen, and Weibin Cai
- Subjects
atherosclerosi ,endothelial FA uptake ,hyperlipidemia ,PEDF ,vascular endothelial growth factor B signaling pathway ,Diseases of the circulatory (Cardiovascular) system ,RC666-701 - Abstract
Background Endothelial cell injury, induced by dyslipidemia, is the initiation of atherosclerosis, resulting in an imbalance in endothelial fatty acid (FA) transport. Pigment epithelial‐derived factor (PEDF) is an important regulator in lipid metabolism. We hypothesized that PEDF is involved in endothelium‐mediated FA uptake under hyperlipidemic conditions. Methods and Results Circulating PEDF levels were higher in patients with atherosclerotic cardiovascular disease than in normal individuals. However, decreasing trends of serum PEDF levels were confirmed in both wild‐type and apolipoprotein E–deficient mice fed a long‐term high‐fat diet. Apolipoprotein E–deficient/PEDF‐deficient mice were generated by crossing PEDF‐deficient mice with apolipoprotein E–deficient mice, and then mice were fed with 24, 36, or 48 weeks of high‐fat diet. Greater increases in body fat and plasma lipids were displayed in PEDF‐deficient mice. In addition, PEDF deficiency in mice accelerated atherosclerosis, as evidenced by increased atherosclerotic plaques, pronounced vascular dysfunction, and increased lipid accumulation in peripheral tissues, whereas injection of adeno‐associated virus encoding PEDF exerted opposite effects. Mechanistically, PEDF inhibited the vascular endothelial growth factor B paracrine signaling by reducing secretion of protein vascular endothelial growth factor B in peripheral tissue cells and decreasing expression of its downstream targets in endothelial cells, including its receptors (namely, vascular endothelial growth factor receptor‐1 and neuropilin‐1), and FA transport proteins 3 and 4, to suppress endothelial FA uptake, whereas PEDF deletion in mice activated the vascular endothelial growth factor B signaling pathway, thus causing markedly increased lipid accumulation. Conclusions Decreasing expression of PEDF aggravates atherosclerosis by significantly impaired vascular function and enhanced endothelial FA uptake, thus exacerbating ectopic lipid deposition in peripheral tissues.
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- 2019
- Full Text
- View/download PDF
7. A novel mouse model of PEDF-associated serious liver inflammation, hepatic tumorigenesis and cardiovascular injury mimics human nonalcoholic steatohepatitis
- Author
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Xinghui Li, Haiping Wang, Yandi Wu, Li Zou, Shijie Deng, Xinlu Fu, Tongsheng Huang, Conghui Shen, Teng Wu, and Weibin Cai
- Subjects
Cell Biology ,Molecular Biology ,Biochemistry ,Genetics (clinical) - Published
- 2023
8. QTL Mapping for Berry Shape Based on a High-density Genetic Map Constructed by Whole-genome Resequencing in Grape
- Author
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Yandi Wu, Yong Wang, Xiucai Fan, Ying Zhang, Jianfu Jiang, Lei Sun, Qiangwei Luo, Feng Sun, and Chonghuai Liu
- Subjects
Ecology ,Renewable Energy, Sustainability and the Environment ,Plant Science ,Biochemistry, Genetics and Molecular Biology (miscellaneous) ,Ecology, Evolution, Behavior and Systematics - Published
- 2022
9. QTL mapping for berry shape based on a high-density genetic map constructed by whole-genome resequencing in grape.
- Author
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Yandi Wu, Yong Wang, Xiucai Fan, Ying Zhang, Jianfu Jiang, Lei Sun, Qiangwei Luo, Feng Sun, and Chonghuai Liu
- Subjects
- *
GRAPE yields , *GENE mapping , *RNA sequencing , *PLANT hormones , *DNA replication - Abstract
Grape berry shape is an important agricultural trait. Clarifying its genetic basis is significant for cultivating grape varieties that meet market demands. However, the current study by forward genetics has not achieved in-depth results. Here, a high-density map was constructed to identify quantitative trait loci (QTLs) for berry shape. A total of 358 709 polymorphic SNPs were obtained using whole-genome resequencing (WGS) based on 208 F2 individuals derived from round grape 'E42-6' and oblong grape 'Rizamat'. The 1 635.65 cM high-density map was divided into 19 linkage groups with an average distance of 0.37 cM. Using this map, three significant QTLs for fruit shape index (ShI: ratio of berry length to berry width) identified over three years were mapped onto LG4 and LG5, including one stable QTL on Chr5 with the genomic region of 0.47e1.94 Mb. Combining with gene annotation and expression patterns based on RNA-seq data from two contrasting F2 individuals with round and oblong berry (their average ShI was 1.89 and 1.10, respectively) at four developmental stages, four candidate genes were selected from the above QTLs. They were mainly involved in DNA replication, cell wall modification, and phytohormone biosynthesis. Further analysis of RNAseq data revealed that several important phytohormone synthesis and metabolic pathways were enriched based on differentially expressed genes (DEGs), which was consistent with the results of QTL mapping for genes related to plant hormone biosynthesis in the F2 population. Furthermore, a comparison of plant hormone content showed that there were significant differences in IAA and tZ content between the two contrasting F2 individuals at different developmental stages. Our findings provide molecular insights into the genetic variation in grape berry shape. Stable QTLs and their tightly linked markers offer the possibility of marker-assisted selection to accelerate berry shape breeding. [ABSTRACT FROM AUTHOR]
- Published
- 2023
- Full Text
- View/download PDF
10. Distinct cardiac energy metabolism and oxidative stress adaptations between obese and non-obese type 2 diabetes mellitus
- Author
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Jingjing Zhao, Saifei Gao, Haiping Wang, Shijie Deng, Ming Yang, Yuanlong Li, Jian Xing Ma, Zhenyu Yang, Yandi Wu, Weibin Cai, Jing Tan, Xinghui Li, Jianding Cheng, Hui Li, and Fengmin Yang
- Subjects
Male ,medicine.medical_specialty ,Diabetic Cardiomyopathies ,Medicine (miscellaneous) ,medicine.disease_cause ,030226 pharmacology & pharmacy ,03 medical and health sciences ,chemistry.chemical_compound ,Mice ,0302 clinical medicine ,Internal medicine ,Diabetic cardiomyopathy ,Lipid droplet ,Medicine ,Animals ,030212 general & internal medicine ,Obesity ,Pharmacology, Toxicology and Pharmaceutics (miscellaneous) ,GSK3B ,Glycogen ,biology ,business.industry ,Myocardium ,Heart ,medicine.disease ,Mice, Inbred C57BL ,Oxidative Stress ,Endocrinology ,Lipotoxicity ,chemistry ,Diabetes Mellitus, Type 2 ,Adipose triglyceride lipase ,biology.protein ,business ,Energy Metabolism ,Oxidative stress ,GLUT4 ,Research Paper ,Heart Failure, Systolic - Abstract
Background: Little is known about the pathophysiological diversity of myocardial injury in type 2 diabetes mellitus (T2DM), but analyzing these differences is important for the accurate diagnosis and precise treatment of diabetic cardiomyopathy. This study aimed to elucidate the key cardiac pathophysiological differences in myocardial injury between obese and non-obese T2DM from mice to humans. Methods: Obese and non-obese T2DM mouse models were successfully constructed and observed until systolic dysfunction occurred. Changes in cardiac structure, function, energy metabolism and oxidative stress were assessed by biochemical and pathological tests, echocardiography, free fatty acids (FFAs) uptake fluorescence imaging, transmission electron microscopy, etc. Key molecule changes were screened and verified by RNA sequencing, quantitative real-time polymerase chain reaction and western blotting. Further, 28 human heart samples of healthy population and T2DM patients were collected to observe the cardiac remodeling, energy metabolism and oxidative stress adaptations as measured by pathological and immunohistochemistry tests. Results: Obese T2DM mice exhibited more severe cardiac structure remodeling and earlier systolic dysfunction than non-obese mice. Moreover, obese T2DM mice exhibited severe and persistent myocardial lipotoxicity, mainly manifested by increased FFAs uptake, accumulation of lipid droplets and glycogen, accompanied by continuous activation of the peroxisome proliferator activated receptor alpha (PPARα) pathway and phosphorylated glycogen synthase kinase 3 beta (p-GSK-3β), and sustained inhibition of glucose transport protein 4 (GLUT4) and adipose triglyceride lipase (ATGL), whereas non-obese mice showed no myocardial lipotoxicity characteristics at systolic dysfunction stage, accompanied by the restored PPARα pathway and GLUT4, sustained inhibition of p-GSK-3β and activation of ATGL. Additionally, both obese and non-obese T2DM mice showed significant accumulation of reactive oxygen species (ROS) when systolic dysfunction occurred, but the NF-E2-related factor 2 (Nrf2) pathway was significantly activated in obese mice, while was significantly inhibited in non-obese mice. Furthermore, the key differences found in animals were reliably verified in human samples. Conclusion: Myocardial injury in obese and non-obese T2DM may represent two different types of complications. Obese T2DM individuals, compared to non-obese individuals, are more prone to develop cardiac systolic dysfunction due to severe and persistent myocardial lipotoxicity. Additionally, anti-oxidative dysfunction may be a key factor leading to myocardial injury in non-obese T2DM.
- Published
- 2020
11. Transcriptome analysis reveals pathogenesis-related gene 1 pathway against salicylic acid treatment in grapevine (Vitis vinifera L).
- Author
-
Ur Rahman, Faiz, Khan, Irshad Ahmad, Aslam, Ali, Ruitao Liu, Lei Sun, Yandi Wu, Aslam, Muhammad Muzammal, Khan, Asad Ullah, Peng Li, Jianfu Jiang, Xiucai Fan, Chonghuai Liu, and Ying Zhang
- Subjects
VITIS vinifera ,SALICYLIC acid ,GRAPES ,REPORTER genes ,PLANT genes ,TRANSCRIPTOMES - Abstract
Salicylic acid (SA) is a well-studied phenolic plant hormone that plays an important role in plant defense against the hemi-biothrophic and biothrophic pathogens and depends on the living cells of host for the successful infection. In this study, a pathogenesis test was performed between Vitis davidii and V. vinifera cultivars against grape white rot disease (Coniella diplodiella). V. davidii was found to be resistant against this disease. SA contents were found to be higher in the resistant grape cultivar after different time points. RNA-seq analysis was conducted on susceptible grapevine cultivars after 12, 24, and 48 h of SA application with the hypothesis that SA may induce defense genes in susceptible cultivars. A total of 511 differentially expressed genes (DEGs) were identified from the RNA-seq data, including some important genes, VvWRKY1/2, VvNPR1, VvTGA2, and VvPR1, for the SA defense pathway. DEGs related to phytohormone signal transduction and flavonoid biosynthetic pathways were also upregulated. The quantitative real-time PCR (qRT-PCR) results of the significantly expressed transcripts were found to be consistent with the transcriptome data, with a high correlation between the two analyses. The pathogenesis-related gene 1 (VvPR1), which is an important marker gene for plant defense, was selected for further promoter analysis. The promoter sequence showed that it contains some important cis-elements (W-box, LS7, as-1, and TCA-element) to recruit the transcription factors VvWRKY, VvNPR1, and VvTGA2 to express the VvPR1 gene in response to SA treatment. Furthermore, the VvPR1 promoter was serially deleted into different fragments (-1,837, -1,443, -1,119, -864, -558, -436, and -192) bp and constructed vectors with the GUS reporter gene. Deletion analysis revealed that the VvPR1 promoter between -1837 bp to -558 bp induced significant GUS expression with respect to the control. On the basis of these results, the -558 bp region was assumed to be an important part of the VvPR1 promoter, and this region contained the important cis-elements related to SA, such as TCAOPEN element (-1,472 bp), LS7 (-1,428 bp), and as-1 (-520 bp), that recruit the TFs and induce the expression of the VvPR1 gene. This study expanded the available information regarding SA-induced defense in susceptible grapes and recognized the molecular mechanisms through which this defense might be mediated. [ABSTRACT FROM AUTHOR]
- Published
- 2022
- Full Text
- View/download PDF
12. Selecting Audio and Visual Stimuli: What Do We Prefer If They Happened Simultaneously?
- Author
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Taojun Zhang, Yandi Wu, and Yutong Ding
- Published
- 2021
13. Abstract 338: Limited Reduction of Heart Rate Promotes Cardiac Regeneration by Switching the Energy Metabolic Mode in Cardiomyocytes
- Author
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Jing Tan, Tongsheng Huang, Yuanlong Li, Ming Yang, Yandi Wu, Conghui Shen, Xinghui Li, Weibin Cai, Shijie Deng, and Haiping Wang
- Subjects
Cardiac regeneration ,Reduction (complexity) ,medicine.medical_specialty ,Physiology ,Chemistry ,Internal medicine ,Heart rate ,Cardiology ,medicine ,Cardiology and Cardiovascular Medicine ,Energy (signal processing) - Abstract
Aims: Lack of cardiac regeneration with robust fibrosis response to the acute myocardial injury is the main obstacle to clinical treatment of cardiovascular diseases in humans. Stimulating the proliferation of endogenous cardiomyocytes (CMs) and replacing the scarred tissue with new functional CMs is a potential therapeutic strategy to the patients with heart failure. Heart rate reduction (HRR) is regarded as an effective clinical treatment for myocardial infarction. However, the mechanism of HRR promoting the recovery of cardiac function after injury still remains controversial, and whether there is any endogenous CM proliferation induced by HRR is undefined. Methods and results: The beating of CMs was reduced in vitro and heart rate (HR) of adult mice and different animal models of myocardial injury were modulated by six antiarrhythmic drugs to determine the role of HR in CM proliferation and cardiac repair. RNA-seq, extracellular flux analysis, metabolic flux analysis, and metabonomics were used to study the CM metabolism after HR modulation. We verified that reducing the beating can induce CM proliferation both in vitro and in vivo physiologically, and HRR also promoted cardiac regenerative repair after myocardial injury as well, reversely, increasing HR showed the opposite effect. Mechanistically, HRR reduced energy metabolism requirements and total ATP production of CMs but switched energy metabolic mode that the proportion of ATP production from aerobic glycolysis was increased, while from fatty acid oxidation was decreased. The switching of energy metabolic mode in CMs occurred in synchrony with the changes of glycolytic enzymes activities, these enzymes, including PFKFB3, PKM2, GAPDH, induced G1/S transition for cell cycle re-entry of CMs by upregulating the expression of cyclin D and CDK4/6 and facilitate substrates into the biomass needed to produce a new cell by biosynthesis. This coordinating function of glycolytic enzymes contributed to CM proliferation. Conclusion: Together, these results demonstrate that reduction of heart rate promotes CM proliferation by switching the energy metabolic mode, and highlight the potential therapeutic role of HRR in regenerative medicine.
- Published
- 2020
14. Pigment Epithelial‐Derived Factor Deficiency Accelerates Atherosclerosis Development via Promoting Endothelial Fatty Acid Uptake in Mice With Hyperlipidemia
- Author
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Weibin Cai, Shijie Deng, Bo Hu, Jing Tan, Ming Yang, Yuanlong Li, Yandi Wu, Fengmin Yang, Yanfang Yang, Zhenyu Yang, Hui Li, Haiping Wang, Hui Chen, Saifei Gao, Yuling Zhang, and Xinghui Li
- Subjects
Male ,Vascular Endothelial Growth Factor B ,Mice, Knockout, ApoE ,030204 cardiovascular system & hematology ,Molecular Cardiology ,Mice ,atherosclerosi ,0302 clinical medicine ,Vascular Disease ,Hyperlipidemia ,Mechanisms ,hyperlipidemia ,Myocytes, Cardiac ,endothelial FA uptake ,Original Research ,Mice, Knockout ,chemistry.chemical_classification ,0303 health sciences ,Fatty Acids ,Middle Aged ,Fatty Acid Transport Proteins ,Endothelial stem cell ,visual_art ,PEDF ,visual_art.visual_art_medium ,Female ,Cardiology and Cardiovascular Medicine ,medicine.medical_specialty ,Hyperlipidemias ,vascular endothelial growth factor B signaling pathway ,03 medical and health sciences ,Pigment ,Internal medicine ,Human Umbilical Vein Endothelial Cells ,medicine ,Animals ,Humans ,Nerve Growth Factors ,Eye Proteins ,Serpins ,Aged ,Dyslipidemias ,030304 developmental biology ,Vascular Endothelial Growth Factor Receptor-1 ,business.industry ,Endothelial Cells ,Fatty acid ,Atherosclerosis ,medicine.disease ,Neuropilin-1 ,Endocrinology ,Animal Models of Human Disease ,chemistry ,Case-Control Studies ,business ,Basic Science Research ,Dyslipidemia - Abstract
Background Endothelial cell injury, induced by dyslipidemia, is the initiation of atherosclerosis, resulting in an imbalance in endothelial fatty acid ( FA ) transport. Pigment epithelial‐derived factor ( PEDF ) is an important regulator in lipid metabolism. We hypothesized that PEDF is involved in endothelium‐mediated FA uptake under hyperlipidemic conditions. Methods and Results Circulating PEDF levels were higher in patients with atherosclerotic cardiovascular disease than in normal individuals. However, decreasing trends of serum PEDF levels were confirmed in both wild‐type and apolipoprotein E–deficient mice fed a long‐term high‐fat diet. Apolipoprotein E–deficient/PEDF‐deficient mice were generated by crossing PEDF‐deficient mice with apolipoprotein E–deficient mice, and then mice were fed with 24, 36, or 48 weeks of high‐fat diet. Greater increases in body fat and plasma lipids were displayed in PEDF ‐deficient mice. In addition, PEDF deficiency in mice accelerated atherosclerosis, as evidenced by increased atherosclerotic plaques, pronounced vascular dysfunction, and increased lipid accumulation in peripheral tissues, whereas injection of adeno‐associated virus encoding PEDF exerted opposite effects. Mechanistically, PEDF inhibited the vascular endothelial growth factor B paracrine signaling by reducing secretion of protein vascular endothelial growth factor B in peripheral tissue cells and decreasing expression of its downstream targets in endothelial cells, including its receptors (namely, vascular endothelial growth factor receptor‐1 and neuropilin‐1), and FA transport proteins 3 and 4, to suppress endothelial FA uptake, whereas PEDF deletion in mice activated the vascular endothelial growth factor B signaling pathway, thus causing markedly increased lipid accumulation. Conclusions Decreasing expression of PEDF aggravates atherosclerosis by significantly impaired vascular function and enhanced endothelial FA uptake, thus exacerbating ectopic lipid deposition in peripheral tissues.
- Published
- 2019
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