Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5504731 | Biochemical and Biophysical Research Communications | 2017 | 7 Pages |
Abstract
Body fat mass is closely associated to diseases related to obesity. MicroRNAs (miRNAs, miR) are important regulatory molecules that function as post-transcriptional gene regulators of adipocyte development. In the current study, we revealed that reduced expression of miR-199a-3p in adipose tissue resulting from high fat diet (HFD)-induced obesity in mice. Overexpression of miR-199a-3p promoted adipocyte proliferation by regulating the expression of regulating factors of the cell cycle. Furthermore, miR-199a-3p blunted lipid accumulation in 3T3-L1 adipocytes. This was accompanied by a marked decrease in the expression of adipocyte-specific genes involved in lipogenic transcription, fatty acid synthesis, and fatty acid transportation. Furthermore, the fatty acid oxidation process was enhanced. Luciferase activity assays confirmed that miR-199a-3p regulates adipocyte differentiation by directly targeting the 3â²-untranslated region (3â²-UTR) of stearoyl-CoA desaturase (SCD). Moreover, miR-199a-3p regulates fatty acid composition by decreasing the ratio of unsaturated fatty acids (UFAs) in adipocytes transfected with miR-199a-3p mimics. These results suggest that miR-199a-3p may promote adipocyte proliferation, while also repressing adipocyte differentiation by down-regulating SCD and changing fatty acid composition during adipogenesis.
Keywords
VLDLACADLMiR-199a-3pHSD11B1FATP4ELOVLC/EBP-αCCAAT/enhancer-binding proteinsACOT1Acss1acyl-CoA oxidase 2Acox2DGATSREBPLPLFASPPAR-γACCACSFABP4AP2GSKacyl-CoA synthetaseacetyl-CoA carboxylasefatty acid synthaseProliferationFatty acid compositionDifferentiationDiacylglycerol acyltransferaseLipoprotein lipasevery-low density lipoproteinfatty acid binding protein 4Sterol regulatory element-binding proteinfatty acid transport protein 4glycogen synthase kinase
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Authors
Zhendong Tan, Jingjing Du, Linyuan Shen, Chendong Liu, Jideng Ma, Lin Bai, Yanzhi Jiang, Guoqing Tang, Mingzhou Li, Xuewei Li, Shunhua Zhang, Li Zhu,