Genistein Promotes Skeletal Muscle Regeneration by Regulating miR-221/222.
Linyuan ShenTianci LiaoJingyun ChenJianfeng MaJinyong WangLei ChenShunhua ZhangYe ZhaoLili NiuChang-Jun ZengMailin GanLi ZhuPublished in: International journal of molecular sciences (2022)
Genistein (GEN), a phytoestrogen, has been reported to regulate skeletal muscle endocrine factor expression and muscle fiber type switching, but its role in skeletal muscle regeneration is poorly understood. As a class of epigenetic regulators widely involved in skeletal muscle development, microRNAs (miRNAs) have the potential to treat skeletal muscle injury. In this study, we identified miR-221 and miR-222 and their target genes MyoG and Tnnc1 as key regulators during skeletal muscle regeneration, and both were regulated by GEN. C2C12 myoblasts and C2C12 myotubes were then used to simulate the proliferation and differentiation of muscle satellite cells during skeletal muscle regeneration. The results showed that GEN could inhibit the proliferation of satellite cells and promote the differentiation of satellite cells by inhibiting the expression of miR-221/222. Subsequent in vitro and in vivo experiments showed that GEN improved skeletal muscle regeneration mainly by promoting satellite cell differentiation in the middle and late stages, by regulating miR-221/222 expression. These results suggest that miR-221/222 and their natural regulator GEN have potential applications in skeletal muscle regeneration.
Keyphrases
- skeletal muscle
- long non coding rna
- cell proliferation
- stem cells
- insulin resistance
- poor prognosis
- long noncoding rna
- induced apoptosis
- signaling pathway
- cell cycle arrest
- gene expression
- transcription factor
- type diabetes
- oxidative stress
- dna methylation
- genome wide
- risk assessment
- metabolic syndrome
- human health
- climate change
- pi k akt