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机械拉伸通过激活C2C12成肌细胞中的NF-κB来调节微小RNA表达谱。

Mechanical stretch regulates microRNA expression profile via NF-κB activation in C2C12 myoblasts.

作者信息

Hua Wenxi, Zhang Mahui, Wang Yongkui, Yu Lei, Zhao Tingting, Qiu Xiaozhong, Wang Leyu

机构信息

Department of Anatomy, Guangdong Provincial Key Laboratory of Construction and Detection in Tissue Engineering, Guangzhou, Guangdong 510515, P.R. China.

Department of Neurology, Zhujiang Hospital, Southern Medical University, Guangzhou, Guangdong 510515, P.R. China.

出版信息

Mol Med Rep. 2016 Dec;14(6):5084-5092. doi: 10.3892/mmr.2016.5907. Epub 2016 Oct 31.

DOI:10.3892/mmr.2016.5907
PMID:27840929
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5355701/
Abstract

MicroRNAs (miRNAs/miRs) and nuclear factor (NF)-κB activation are involved in mechanical stretch-induced skeletal muscle regeneration. However, there are a small number of miRNAs that have been reported to be associated with NF‑κB activation during mechanical stretch-induced myogenesis. In the present study, C2C12 myoblasts underwent cyclic mechanical stretch in vitro, to explore the relationship between miRNA expression and NF‑κB activation during stretch-mediated myoblast proliferation. The results revealed that 10% deformation, 0.125 Hz cyclic mechanical stretch could promote myoblast proliferation. The miRNA expression profile was subsequently altered; miR‑500, ‑1934, ‑31, ‑378, ‑331 and ‑5097 were downregulated, whereas miR‑1941 was upregulated. These miRNAs were all involved in stretch‑mediated myoblast proliferation. Notably, the expression of these miRNAs was reversed following treatment of 0.125 Hz mechanically stretched C2C12 cells with NF‑κB inhibitors, which was accompanied by C2C12 cell growth suppression. Therefore, the present study is the first, to the best of our knowledge, to demonstrate that the NF‑κB‑dependent miRNA profile is associated with mechanical stretch-induced myoblast proliferation.

摘要

微小RNA(miRNA/miR)与核因子(NF)-κB激活参与机械拉伸诱导的骨骼肌再生。然而,据报道,在机械拉伸诱导的成肌过程中,仅有少数miRNA与NF-κB激活有关。在本研究中,C2C12成肌细胞在体外进行周期性机械拉伸,以探讨拉伸介导的成肌细胞增殖过程中miRNA表达与NF-κB激活之间的关系。结果显示,10%变形、0.125Hz的周期性机械拉伸可促进成肌细胞增殖。随后miRNA表达谱发生改变;miR-500、-1934、-31、-378、-331和-5097表达下调,而miR-1941表达上调。这些miRNA均参与拉伸介导的成肌细胞增殖。值得注意的是,在用NF-κB抑制剂处理0.125Hz机械拉伸的C2C12细胞后,这些miRNA的表达发生逆转,同时C2C12细胞生长受到抑制。因此,据我们所知,本研究首次证明依赖NF-κB的miRNA谱与机械拉伸诱导的成肌细胞增殖有关。

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