Walsh K, Perlman H
Division of Cardiovascular Research, St Elizabeth's Medical Center, Tufts University School of Medicine, Boston, Massachusetts, USA.
Curr Opin Genet Dev. 1997 Oct;7(5):597-602. doi: 10.1016/s0959-437x(97)80005-6.
Myogenic precursor cells withdraw irreversibly from the cell cycle as they differentiate into mature myotubes. Cell cycle exit occurs early during the differentiation program and is required for normal expression of the contractile phenotype. Differentiated myocytes also display a decreased propensity to undergo apoptotic cell death. The upregulation of the cyclin-dependent kinase inhibitor p21 and the dephosphorylation of retinoblastoma protein (pRb) appear to be critical regulatory events for the establishment of both the postmitotic and apoptosis-resistant states. The coordinated regulation of cell proliferation and death provides the developing embryo with a mechanism for controlling muscle mass and thereby the size of individual motor units.
生肌前体细胞在分化为成熟肌管时不可逆地退出细胞周期。细胞周期退出发生在分化程序的早期,是收缩表型正常表达所必需的。分化的心肌细胞发生凋亡性细胞死亡的倾向也降低。细胞周期蛋白依赖性激酶抑制剂p21的上调和视网膜母细胞瘤蛋白(pRb)的去磷酸化似乎是建立有丝分裂后和抗凋亡状态的关键调节事件。细胞增殖和死亡的协调调节为发育中的胚胎提供了一种控制肌肉质量从而控制单个运动单位大小的机制。