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微小 RNA-139-5p 通过抑制钙调神经磷酸酶/NFAT 信号通路抑制肌球蛋白重链 I 和 IIa 的表达。

MicroRNA-139-5p suppresses myosin heavy chain I and IIa expression via inhibition of the calcineurin/NFAT signaling pathway.

机构信息

Key Laboratory for Animal Disease-Resistance Nutrition of China Ministry of Education, Institute of Animal Nutrition, Sichuan Agricultural University, Chengdu, Sichuan 611130, PR China.

Key Laboratory for Animal Disease-Resistance Nutrition of China Ministry of Education, Institute of Animal Nutrition, Sichuan Agricultural University, Chengdu, Sichuan 611130, PR China.

出版信息

Biochem Biophys Res Commun. 2018 Jun 12;500(4):930-936. doi: 10.1016/j.bbrc.2018.04.202. Epub 2018 Apr 30.

Abstract

MicroRNAs (miRNAs) are a class of small non-coding RNAs that are widely involved in a variety of biological processes. Different skeletal muscle fiber type composition exhibits characteristic differences in functional properties and energy metabolism of skeletal muscle. However, the molecular mechanism by which miRNAs control the different type of muscle fiber formation is still not fully understood. In the present study, we characterized the role of microRNA-139-5p (miR-139-5p) in the regulation of myosin heavy chain (MyHC) isoform expression and its underlying mechanisms. Here we found that the expression of miR-139-5p was significantly higher in mouse slow-twitch muscle than in fast-twitch muscle. Overexpression of miR-139-5p downregulated the expression of MyHC I and MyHC IIa, whereas inhibition of miR-139-5p upregulated them. We also found that the levels of calcineurin (CaN), NFATc1, MEF2C and MCIP1.4, which are the components of CaN/NFAT signaling pathway that has shown to positively regulate slow fiber-selective gene expression, were notably inhibited by miR-139-5p overexpression. Furthermore, treatment of phenylephrine (PE), a α1-adrenoceptor agonist, abolished the inhibitory effect of miR-139-5p on MyHC I and MyHC IIa expression. Together, our findings indicated that the role of miR-139-5p in regulating the MyHC isoforms, especially MyHC I and MyHC IIa, may be achieved through inhibiting CaN/NFAT signaling pathway.

摘要

微小 RNA(miRNAs)是一类广泛参与多种生物过程的小非编码 RNA。不同的骨骼肌纤维类型组成表现出骨骼肌功能特性和能量代谢的特征差异。然而,miRNAs 控制不同类型肌纤维形成的分子机制尚不完全清楚。在本研究中,我们研究了 microRNA-139-5p(miR-139-5p)在调节肌球蛋白重链(MyHC)同工型表达中的作用及其潜在机制。我们发现 miR-139-5p 在小鼠慢肌中的表达明显高于快肌。miR-139-5p 的过表达下调了 MyHC I 和 MyHC IIa 的表达,而 miR-139-5p 的抑制则上调了它们的表达。我们还发现钙调神经磷酸酶(CaN)、NFATc1、肌细胞增强因子 2C(MEF2C)和 MCIP1.4 的水平,这些是钙调神经磷酸酶/NFAT 信号通路的组成部分,该信号通路已显示出对慢纤维选择性基因表达的正向调节作用,被 miR-139-5p 的过表达显著抑制。此外,α1-肾上腺素能受体激动剂苯肾上腺素(PE)的处理消除了 miR-139-5p 对 MyHC I 和 MyHC IIa 表达的抑制作用。综上所述,我们的研究结果表明,miR-139-5p 在调节 MyHC 同工型,特别是 MyHC I 和 MyHC IIa 中的作用可能是通过抑制 CaN/NFAT 信号通路实现的。

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