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微小RNA-199a靶向脂肪酸转运蛋白1基因并抑制C2C12成肌细胞的脂肪生成转分化。

MicroRNA-199a Targets the Fatty Acid Transport Protein 1 Gene and Inhibits the Adipogenic Trans-Differentiation of C2C12 Myoblasts.

作者信息

Qi Renli, Long Dingbiao, Wang Jing, Wang Qi, Huang Xiaofeng, Cao Chunting, Gao Guangliang, Huang Jinxiu

机构信息

Chongqing Academy of Animal Science, Rongchang, China.

出版信息

Cell Physiol Biochem. 2016;39(3):1087-97. doi: 10.1159/000447817. Epub 2016 Aug 26.

Abstract

BACKGROUND/AIMS: Muscle cells are able to trans-differentiate into adipocytes with adipogenesis induction. MicroRNAs (miRNAs), a class of small non-coding RNAs, widely participate in the regulation of growth and development of cells. However, the expression and regulatory role of miRNAs in the trans-differentiation of muscle cell are largely unknown.

METHODS

C2C12 myoblasts were inducted to adipogenesis trans-differentiation and microarrays were used to assay the changes of expression profile of miRNAs. MiR-199a, a miRNA showed significant change in the trans-differentiation, was selected for the subsequent function study via over- expression and knock down.

RESULTS

Dozens of miRNAs showed different changes followed the adipogenesis trans-differentiation of C2C12 cells. In which, miR-199a was decreased in the adipogenic cells and miR-199a over-expression inhibited the trans-differentiation and decreased lipid accumulation in the cells. Moreover, Fatty acid transport protein 1 (Fatp1), a major regulator of trans-membrane transportation and the oxidative metabolism of free fatty acids, was showed to be a target of miR-199a by computational and luciferase reporter assays. Additionally, Fatp1 knock-down by small interfering RNA had similar inhibitory effects on the trans-differentiation in C2C12 cells.

CONCLUSION

Our study reveals an important role for miR-199a in the regulation of adipogenic trans-differentiation in muscle cells via suppression of Fatp1 gene.

摘要

背景/目的:在脂肪生成诱导下,肌肉细胞能够转分化为脂肪细胞。微小RNA(miRNA)是一类小的非编码RNA,广泛参与细胞生长和发育的调控。然而,miRNA在肌肉细胞转分化中的表达及调控作用很大程度上尚不清楚。

方法

诱导C2C12成肌细胞进行脂肪生成转分化,并用微阵列分析miRNA表达谱的变化。选择在转分化过程中表现出显著变化的miR-199a,通过过表达和敲低进行后续功能研究。

结果

数十种miRNA在C2C12细胞脂肪生成转分化过程中表现出不同变化。其中,miR-199a在脂肪生成细胞中表达降低,miR-199a过表达抑制转分化并减少细胞内脂质积累。此外,通过计算和荧光素酶报告基因分析表明,脂肪酸转运蛋白1(Fatp1)是跨膜运输和游离脂肪酸氧化代谢的主要调节因子,也是miR-199a的靶标。另外,用小干扰RNA敲低Fatp1对C2C12细胞的转分化具有类似的抑制作用。

结论

我们的研究揭示了miR-199a通过抑制Fatp1基因在调节肌肉细胞脂肪生成转分化中起重要作用。

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