中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
miR-212-5p suppresses lipid accumulation by targeting FAS and SCD1

文献类型:期刊论文

作者Guo, Yajie; Yu, Junjie; Wang, Chunxia; Li, Kai; Liu, Bin; Du, Ying; Xiao, Fei; Chen, Shanghai; Guo, Feifan; ,
刊名JOURNAL OF MOLECULAR ENDOCRINOLOGY
出版日期2017
卷号59期号:3页码:205-217
关键词miR-212-5p FAS SCD1 lipid accumulation NAFLD
ISSN号0952-5041
DOI10.1530/JME-16-0179
文献子类Article
英文摘要MicroRNAs, a class of small noncoding RNAs, are implicated in controlling a variety of biological processes. We have shown that leucine deprivation suppresses lipogenesis by inhibiting fatty acid synthase (FAS) expression in the liver previously; the aim of our current study is to investigate which kind of microRNA is involved in the regulation of FAS expression in response to leucine deprivation. Here, we indicated that microRNA212-5p specifically binds to mouse FAS 3' UTR and inhibits its activity. Leucine deficiency significantly increased the mRNA levels of miR-212-5p in the livers of mice. Further studies proved that miR-212-5p also directly binds to the 3' UTR of stearoyl-CoA desaturase-1 (SCD1) to inhibit its activity. Overexpression of miR-212-5p decreases the protein levels of FAS and SCD1 in vitro and in vivo, and silencing of miR-212-5p has the opposite effects in mouse primary hepatocytes. Moreover, overexpression of miR-212-5p significantly decreases triglyceride (TG) accumulation in primary hepatocytes and in the livers of mice injected with adenovirus-mediated overexpressing of miR-212-5p (Ad-miR-212). Interestingly, inhibition of miR-212-5p reverses the suppressive effects of leucine deficiency on FAS and SCD1 expression, as well as TG accumulation in mouse primary hepatocytes. Finally, we demonstrate that leucine deficiency induces the expression of miR-212-5p in a GCN2/ATF4-dependent manner. Taken together, our results demonstrate a novel function of hepatic miR-212-5p in the regulation of lipid metabolism which represents a potential therapeutic target for the treatment of non-alcohol fatty liver diseases (NAFLD).
学科主题Endocrinology & Metabolism
WOS关键词FATTY LIVER-DISEASE ; DE-NOVO LIPOGENESIS ; INSULIN-RESISTANCE ; HEPATIC STEATOSIS ; AMINO-ACID ; MICRORNA EXPRESSION ; METABOLIC SYNDROME ; GCN2/ATF4 PATHWAY ; BINDING-PROTEIN ; X RECEPTOR
语种英语
WOS记录号WOS:000417615000004
出版者BIOSCIENTIFICA LTD
版本出版稿
源URL[http://202.127.25.144/handle/331004/1225]  
专题中国科学院上海生命科学研究院营养科学研究所
作者单位Univ Chinese Acad Sci, Chinese Acad Sci, Inst Nutr Sci, Key Lab Nutr & Metab,Shanghai Inst Biol Sci, Shanghai, Peoples R China,
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Guo, Yajie,Yu, Junjie,Wang, Chunxia,et al. miR-212-5p suppresses lipid accumulation by targeting FAS and SCD1[J]. JOURNAL OF MOLECULAR ENDOCRINOLOGY,2017,59(3):205-217.
APA Guo, Yajie.,Yu, Junjie.,Wang, Chunxia.,Li, Kai.,Liu, Bin.,...&,.(2017).miR-212-5p suppresses lipid accumulation by targeting FAS and SCD1.JOURNAL OF MOLECULAR ENDOCRINOLOGY,59(3),205-217.
MLA Guo, Yajie,et al."miR-212-5p suppresses lipid accumulation by targeting FAS and SCD1".JOURNAL OF MOLECULAR ENDOCRINOLOGY 59.3(2017):205-217.

入库方式: OAI收割

来源:上海营养与健康研究所

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