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Sesn2的抑制对C2C12成肌细胞的肌源性分化具有负调控作用。

Inhibition of Sesn2 has negative regulatory effects on the myogenic differentiation of C2C12 myoblasts.

作者信息

Song Zubiao, Lin Qing, Liang Jiahui, Zhang Weixi

机构信息

Department of Neurology, The First Affiliated Hospital, Sun Yat-Sen University; Guangdong Provincial Key Laboratory of Diagnosis and Treatment of Major Neurological Diseases; National Key Clinical Department and Key Discipline of Neurology, No. 58 Zhongshan Road 2, Guangzhou, 510080, China.

出版信息

Mol Biomed. 2024 Aug 9;5(1):31. doi: 10.1186/s43556-024-00193-z.

Abstract

Sestrin2 (Sesn2) has been previously confirmed to be a stress-response molecule. However, the influence of Sesn2 on myogenic differentiation remains elusive. This study was conducted to analyze the role of Sesn2 in the myogenic differentiation of C2C12 myoblasts and related aspects in mdx mice, an animal model of Duchenne muscular dystrophy (DMD). Our results showed that knockdown of Sesn2 reduced the myogenic differentiation capacity of C2C12 myoblasts. Predictive analysis from two databases suggested that miR-182-5p is a potential regulator of Sesn2. Further experimental validation revealed that overexpression of miR-182-5p decreased both the protein and mRNA levels of Sesn2 and inhibited myogenesis of C2C12 myoblasts. These findings suggest that miR-182-5p negatively regulates myogenesis by repressing Sesn2 expression. Extending to an in vivo model of DMD, knockdown of Sesn2 led to decreased Myogenin (Myog) expression and increased Pax7 expression, while its overexpression upregulated Myog levels and enhanced the proportion of slow-switch myofibers. These findings indicate the crucial role of Sesn2 in promoting myogenic differentiation and skeletal muscle regeneration, providing potential therapeutic targets for muscular dystrophy.

摘要

硒蛋白2(Sesn2)先前已被证实是一种应激反应分子。然而,Sesn2对成肌分化的影响仍不清楚。本研究旨在分析Sesn2在C2C12成肌细胞成肌分化中的作用以及在杜氏肌营养不良症(DMD)动物模型mdx小鼠中的相关情况。我们的结果表明,敲低Sesn2会降低C2C12成肌细胞的成肌分化能力。两个数据库的预测分析表明,miR-182-5p是Sesn2的潜在调节因子。进一步的实验验证表明,miR-182-5p的过表达降低了Sesn2的蛋白质和mRNA水平,并抑制了C2C12成肌细胞的肌生成。这些发现表明,miR-182-5p通过抑制Sesn2表达对肌生成产生负调控作用。延伸至DMD的体内模型,敲低Sesn2导致生肌调节因子(Myog)表达降低,配对盒蛋白7(Pax7)表达增加,而其过表达则上调了Myog水平并增加了慢转换肌纤维的比例。这些发现表明Sesn2在促进成肌分化和骨骼肌再生中起关键作用,为肌肉营养不良症提供了潜在的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3fa5/11310181/f4a98afd9bf6/43556_2024_193_Fig1_HTML.jpg

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