Johnson S E, Allen R E
Department of Animal Sciences, University of Arizona, Tucson 85721.
Exp Cell Res. 1990 Apr;187(2):250-4. doi: 10.1016/0014-4827(90)90088-r.
A new skeletal muscle cell line, rat myoblast omega or RMo, has been characterized with regard to the effects of three growth factors: basic fibroblast growth factor (bFGF), insulin-like growth factor I (IGF-I), and transforming growth factor beta (TGF-beta). Results indicate a differential response of these factors on both cell proliferation and differentiation. Exposure to bFGF and IGF-I stimulate proliferation, while TGF-beta has no effect on cell number. RMo cell differentiation, as indicated by skeletal myosin synthesis, is enhanced by IGF-I, whereas both bFGF and TGF-beta suppress differentiation. These responses are in agreement with the effects of bFGF, IGF-I, and TGF-beta on myogenic cells cultured from fetal and postnatal muscle, thereby suggesting that RMo cells can serve as a model system for the study of growth factor effects on skeletal muscle cells.
一种新的骨骼肌细胞系,大鼠成肌细胞ω或RMo,已就三种生长因子的作用进行了表征:碱性成纤维细胞生长因子(bFGF)、胰岛素样生长因子I(IGF-I)和转化生长因子β(TGF-β)。结果表明这些因子对细胞增殖和分化有不同的反应。暴露于bFGF和IGF-I会刺激增殖,而TGF-β对细胞数量没有影响。如骨骼肌肌球蛋白合成所示,IGF-I可增强RMo细胞分化,而bFGF和TGF-β均抑制分化。这些反应与bFGF、IGF-I和TGF-β对从胎儿和出生后肌肉培养的成肌细胞的作用一致,从而表明RMo细胞可作为研究生长因子对骨骼肌细胞作用的模型系统。