Li X, McFarland D C, Velleman S G
Departament of Animal Sciences, Ohio Agricultural Research and Development Center, The Ohio State University, Wooster 44691, USA.
Poult Sci. 2006 Feb;85(2):326-32. doi: 10.1093/ps/85.2.326.
Myoblast-extracellular matrix interactions play a pivotal role in skeletal muscle development. Transforming growth factor-beta (TGF-beta) is a key regulator of muscle cell proliferation and differentiation. The level of TGF-beta expressed will affect the concentration of the extracellular matrix proteoglycan decorin and the cell surface beta1 integrin subunit. The decorin proteoglycan is a regulator of cell growth as well as the organization of the extracellular matrix. The beta1 integrin plays a role in muscle cell attachment, migration, and the formation of multinucleated myotubes. In the current study, chicken myogenic satellite cells isolated from the pectoralis major muscle from the chicken genetic muscle weakness, low score normal (LSN), and normal pectoralis major muscle were used to investigate TGF-beta expression as it relates to decorin and beta1 integrin mRNA expression. The LSN muscle defect is characterized by altered myotube formation and sarcomere structure, and the satellite cells have reduced proliferation and differentiation. The mRNA expression was measured by real-time quantitative reverse transcription PCR. The LSN condition has elevated expression of TGF-beta2 and TGF-beta4 with increased expression of decorin and decreased beta1 integrin during myogenic satellite cell proliferation and differentiation. Normal satellite cell cultures were treated with the addition of exogenous TGF-beta during differentiation to determine if the altered expression of LSN decorin and beta1 integrin was associated with TGF-beta expression. The addition of exogenous TGF-beta decreased decorin expression during differentiation and reduced beta1 integrin expression at 24 and 48 h of differentiation. These results suggested that alteration of decorin expression in the LSN myogenic satellite cells may occur by a mechanism involving factors in addition to TGF-beta, but the addition of exogenous TGF-beta did affect both decorin and beta1 integrin expression. These data, therefore, suggested that TGF-beta might play a pivotal role in chicken skeletal muscle formation through modulation of the expression of both extracellular matrix molecules and cellular receptors important in the control of cell migration and growth regulation.
成肌细胞与细胞外基质的相互作用在骨骼肌发育中起关键作用。转化生长因子-β(TGF-β)是肌肉细胞增殖和分化的关键调节因子。TGF-β的表达水平会影响细胞外基质蛋白聚糖核心蛋白聚糖和细胞表面β1整合素亚基的浓度。核心蛋白聚糖是细胞生长以及细胞外基质组织的调节因子。β1整合素在肌肉细胞附着、迁移和多核肌管的形成中发挥作用。在本研究中,从患有遗传性肌肉无力的鸡的胸大肌、低评分正常(LSN)和正常胸大肌中分离出鸡成肌卫星细胞,以研究TGF-β表达与核心蛋白聚糖和β1整合素mRNA表达的关系。LSN肌肉缺陷的特征是肌管形成和肌节结构改变,卫星细胞的增殖和分化减少。通过实时定量逆转录PCR测量mRNA表达。在成肌卫星细胞增殖和分化过程中,LSN状态下TGF-β2和TGF-β4的表达升高,核心蛋白聚糖表达增加,β1整合素表达降低。在分化过程中,对正常卫星细胞培养物添加外源性TGF-β,以确定LSN核心蛋白聚糖和β1整合素的表达改变是否与TGF-β表达有关。添加外源性TGF-β在分化过程中降低了核心蛋白聚糖的表达,并在分化24小时和48小时时降低了β1整合素的表达。这些结果表明,LSN成肌卫星细胞中核心蛋白聚糖表达的改变可能通过涉及TGF-β以外因素的机制发生,但添加外源性TGF-β确实影响了核心蛋白聚糖和β1整合素的表达。因此,这些数据表明,TGF-β可能通过调节细胞外基质分子和细胞受体的表达在鸡骨骼肌形成中起关键作用,这些分子和受体在控制细胞迁移和生长调节中很重要。