Jones N C, Fedorov Y V, Rosenthal R S, Olwin B B
Department of Molecular, Cellular, and Developmental Biology, University of Colorado, Boulder 80309, USA.
J Cell Physiol. 2001 Jan;186(1):104-15. doi: 10.1002/1097-4652(200101)186:1<104::AID-JCP1015>3.0.CO;2-0.
Skeletal muscle satellite cells, which are found between the muscle fiber and the basal lamina, remain quiescent and undifferentiated unless stimulated to remodel skeletal muscle or repair injured skeletal muscle tissue. Quiescent satellite cells express c-met and fibroblast growth factor receptors (FGFR) 1 and 4, suggesting these receptors are involved in maintaining the undifferentiated quiescent state or involved in satellite cell activation. Although the signaling pathways involved are poorly understood, the mitogen activated protein kinase (MAPK) cascade has been implicated in the regulation of skeletal muscle growth and differentiation by FGFs. In this study, we investigated if activation of the Raf-MKK1/2-ERK1/2 signaling cascade plays a role in FGF-dependent repression of differentiation and proliferation of MM14 cells, a skeletal muscle satellite cell line. Inactivation ofthe Raf-MKK1/2-ERK1/2 pathway in myoblasts through the overexpression of dominant negative mutants of Raf-1 blocks ERK1/2 activity and prevents myoblast proliferation. Additionally, inhibition of MKK1/2 by treatment with pharmacological inhibitors also blocks FGF-mediated stimulation of ERK1/2 and blocks the G1 to S phase transition of myoblasts. Unexpectedly, we found that inactivation of the Raf-ERK pathway does not activate a muscle reporter, nor does inactivation of this pathway promote myogenic differentiation. We conclude that FGF-stimulated ERK1/2 signaling is required during the G1 phase of the cell cycle for commitment of myoblasts to DNA synthesis but is not required for mitosis once cells have entered the S-phase. Moreover, ERK1/2 signaling is not required either to repress differentiation, to promote skeletal muscle gene expression, or to promote myoblast fusion.
骨骼肌卫星细胞位于肌纤维和基膜之间,除非受到刺激以重塑骨骼肌或修复受损的骨骼肌组织,否则它们会保持静止和未分化状态。静止的卫星细胞表达c-met和成纤维细胞生长因子受体(FGFR)1和4,这表明这些受体参与维持未分化的静止状态或参与卫星细胞的激活。尽管所涉及的信号通路尚不清楚,但丝裂原活化蛋白激酶(MAPK)级联反应已被认为与FGFs对骨骼肌生长和分化的调节有关。在本研究中,我们调查了Raf-MKK1/2-ERK1/2信号级联反应的激活是否在FGF依赖的MM14细胞(一种骨骼肌卫星细胞系)的分化和增殖抑制中发挥作用。通过过表达Raf-1的显性负性突变体使成肌细胞中的Raf-MKK1/2-ERK1/2通路失活,可阻断ERK1/2活性并阻止成肌细胞增殖。此外,用药物抑制剂处理抑制MKK1/2也可阻断FGF介导的ERK1/2刺激,并阻断成肌细胞从G1期到S期的转变。出乎意料的是,我们发现Raf-ERK通路的失活既不会激活肌肉报告基因,也不会促进成肌分化。我们得出结论,在细胞周期的G1期,FGF刺激的ERK1/2信号对于成肌细胞进行DNA合成是必需的,但一旦细胞进入S期,有丝分裂则不需要该信号。此外,ERK1/2信号对于抑制分化、促进骨骼肌基因表达或促进成肌细胞融合也不是必需的。