Qi Renli, Long Dingbiao, Wang Jing, Wang Qi, Huang Xiaofeng, Cao Chunting, Gao Guangliang, Huang Jinxiu
Chongqing Academy of Animal Science, Rongchang, China.
Cell Physiol Biochem. 2016;39(3):1087-97. doi: 10.1159/000447817. Epub 2016 Aug 26.
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.
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.
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.
Our study reveals an important role for miR-199a in the regulation of adipogenic trans-differentiation in muscle cells via suppression of Fatp1 gene.
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。
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。
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。
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。