The role of satellite cell-derived TRIM28 in mechanical load- and injury-induced myogenesis.
Kuan-Hung LinJamie E HibbertJake L LemensMelissa M TorbeyNathaniel D SteinertPhilip M FlejsierowiczKiley M MelkaMarcos LaresVijayasaradhi SetaluriTroy A HornbergerPublished in: bioRxiv : the preprint server for biology (2023)
Satellite cells are skeletal muscle stem cells that contribute to postnatal muscle growth, and they endow skeletal muscle with the ability to regenerate after a severe injury. Here we discovered that this myogenic potential of satellite cells requires a protein called tripartite motif-containing 28 (TRIM28). Unexpectedly, multiple lines of both in vitro and in vivo evidence revealed that the myogenic function of TRIM28 is not dependent on changes in the phosphorylation of its serine 473 residue. Moreover, the functions of TRIM28 were not mediated through the regulation of satellite cell proliferation or differentiation. Instead, our findings indicate that TRIM28 regulates the ability of satellite cells to progress through the process of fusion. Specifically, we discovered that TRIM28 controls the expression of a fusogenic protein called myomixer and concomitant fusion pore formation. Collectively, the outcomes of this study expose the framework of a novel regulatory pathway that is essential for myogenesis.
Keyphrases
- skeletal muscle
- induced apoptosis
- stem cells
- cell cycle arrest
- cell proliferation
- insulin resistance
- endoplasmic reticulum stress
- poor prognosis
- binding protein
- signaling pathway
- type diabetes
- transcription factor
- pi k akt
- bone marrow
- cell cycle
- preterm infants
- adipose tissue
- single cell
- protein kinase
- high glucose
- diabetic rats
- early onset