蛋白质组
骨骼肌
肌发生
细胞生物学
激酶
心肌细胞
蛋白激酶A
PI3K/AKT/mTOR通路
磷酸蛋白质组学
C2C12型
化学
生物
信号转导
生物化学
内分泌学
蛋白质磷酸化
作者
Ben Stocks,Júlia Prats Quesada,Anthony M. Mozzicato,Carolina dos Santos Jacob,Simone Jensen,Kirstin A. MacGregor,Jens Bangsbo,Juleen R. Zierath,Morten Hostrup,Atul S. Deshmukh
出处
期刊:Science Advances
[American Association for the Advancement of Science]
日期:2025-01-31
卷期号:11 (5)
被引量:1
标识
DOI:10.1126/sciadv.adp8608
摘要
The skeletal muscle interstitial space is the extracellular region around myofibers and mediates cross-talk between resident cell types. We applied a proteomic workflow to characterize the human skeletal muscle interstitial fluid proteome at rest and in response to exercise. Following exhaustive exercise, markers of skeletal muscle damage accumulate in the interstitial space followed by the appearance of immune cell–derived proteins. Among the proteins up-regulated after exercise, we identified cathelicidin-related antimicrobial peptide (CAMP) as a bioactive molecule regulating muscle fiber development. Treatment with the bioactive peptide derivative of CAMP (LL-37) resulted in the growth of larger C2C12 skeletal muscle myotubes. Phosphoproteomics revealed that LL-37 activated pathways central to muscle growth and proliferation, including phosphatidylinositol 3-kinase, AKT serine/threonine kinase 1, mitogen-activated protein kinases, and mammalian target of rapamycin. Our findings provide a proof of concept that the interstitial fluid proteome is quantifiable via microdialysis sampling in vivo. These data highlight the importance of cellular communication in the adaptive response to exercise.
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