NFAT公司
肌球蛋白
小RNA
基因亚型
钙调神经磷酸酶
细胞生物学
信号转导
骨骼肌
下调和上调
生物
基因表达
化学
基因表达调控
MEF2C公司
转录因子
基因
生物化学
内分泌学
内科学
医学
移植
作者
Meng Xu,Xiaoling Chen,Zhiqing Huang,Daiwen Chen,Bing Yu,Hong Chen,Jun He,Ping Zheng,Junqiu Luo,Jie Yu,Yuheng Luo
标识
DOI:10.1016/j.bbrc.2018.04.202
摘要
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.
科研通智能强力驱动
Strongly Powered by AbleSci AI