Xu Yanli, Zhao Chaoxian, Sun Xuewen, Liu Zhijun, Zhang Jianzhong
Affiliated Hospital of Hebei Engineering University, Handan, 056002, Hebei, China.
Medical College of Hebei Engineering University, Handan, 056002, Hebei, China.
Biochem Biophys Res Commun. 2015 Nov 6;467(1):103-8. doi: 10.1016/j.bbrc.2015.09.113. Epub 2015 Sep 25.
MicroRNAs (miRNAs) have been suggested to play critical roles in skeletal muscle in response to exercise. Previous study has shown that miR-761 was involved in a novel model regulating the mitochondrial network. However, its role in mitochondrial biogenesis remains poorly understood. Therefore, the current study was aimed to examine the effect of miR-761 on mitochondrial biogenesis in skeletal muscle. Real-time quantitative PCR analysis demonstrated that aberrantly expressed miR-761 is involved in exercise activity and miR-761 is decreased by exercise training compared with the sedentary control mice. miR-761 suppresses mitochondrial biogenesis of C2C12 myocytes by targeting the 3'-UTR of peroxisome proliferator-activated receptor gamma (PPARγ) coactivator-1 (PGC-1α). Overexpression of miR-761 was capable of inhibiting the protein expression levels of PGC-1α. Moreover, miR-761 overexpression suppressed the p38 MAPK signaling pathway and down-regulated the expression of phosphorylated MAPK-activated protein kinase-2 (P-MK2), a downstream kinase of p38 MAPK. The phosphorylation of activating transcription factors 2 (ATF2) that plays a functional role in linking the activation of the p38 MAPK pathway to enhanced transcription of the PGC-1α was also inhibited by the overexpression of miR-761. These findings revealed a novel regulation mechanism for miR-761 in skeletal myocytes, and contributed to a better understanding of the modulation of skeletal muscle in response to exercise.
微小RNA(miRNA)已被认为在骨骼肌对运动的反应中起关键作用。先前的研究表明,miR-761参与了一种调节线粒体网络的新模型。然而,其在线粒体生物发生中的作用仍知之甚少。因此,本研究旨在探讨miR-761对骨骼肌线粒体生物发生的影响。实时定量PCR分析表明,异常表达的miR-761参与运动活动,与久坐不动的对照小鼠相比,运动训练可使miR-761降低。miR-761通过靶向过氧化物酶体增殖物激活受体γ(PPARγ)共激活因子-1(PGC-1α)的3'-非翻译区来抑制C2C12肌细胞的线粒体生物发生。miR-761的过表达能够抑制PGC-1α的蛋白表达水平。此外,miR-761的过表达抑制了p38丝裂原活化蛋白激酶(MAPK)信号通路,并下调了p38 MAPK的下游激酶磷酸化丝裂原活化蛋白激酶激活的蛋白激酶-2(P-MK2)的表达。miR-761的过表达还抑制了在将p38 MAPK途径的激活与PGC-1α转录增强联系起来中起功能作用的激活转录因子2(ATF2)的磷酸化。这些发现揭示了miR-761在骨骼肌细胞中的一种新的调控机制,有助于更好地理解骨骼肌对运动的调节。