Metabolic reprogramming as a novel regulator of skeletal muscle development and regeneration

被引:65
|
作者
Ryall, James G. [1 ]
机构
[1] Univ Melbourne, Melbourne, Vic 3010, Australia
基金
英国医学研究理事会; 美国国家卫生研究院;
关键词
cell fate; glycolysis; metabolism; satellite cells; stem cells; STEM-CELL; PYRUVATE-KINASE; SATELLITE CELLS; MYOBLAST DIFFERENTIATION; SELF-RENEWAL; AMPK; SIRT1; ENERGY; NICHE; PKM2;
D O I
10.1111/febs.12189
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Adult skeletal muscle contains a resident population of stem cells, termed satellite cells, that exist in a quiescent state. In response to an activating signal (such as physical trauma), satellite cells enter the cell cycle and undergo multiple rounds of proliferation, followed by differentiation, fusion, and maturation. Over the last 10-15years, our understanding of the transcriptional regulation of this stem cell population has greatly expanded, but there remains a dearth of knowledge with regard to the initiating signal leading to these changes in transcription. The recent renewed interest in the metabolic regulation of both cancer and stem cells, combined with previous findings indicating that satellite cells preferentially colocalize with blood vessels, suggests that satellite cell function may be regulated by changes in cellular metabolism. This review aims to describe what is currently known about satellite cell metabolism during changes in cell fate, as well as to describe some of the exciting findings in other cell types and how these might relate to satellite cells.
引用
收藏
页码:4004 / 4013
页数:10
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