Van der Loop F T, Van Eys G J, Schaart G, Ramaekers F C
Department of Molecular Cell Biology and Genetics, Cardiovascular Research Institute Maastricht, University of Limburg, The Netherlands.
J Muscle Res Cell Motil. 1996 Feb;17(1):23-36. doi: 10.1007/BF00140321.
Established myogenic cell lines of different species and tissue origin have been used to study expression and organisation of muscle-specific proteins during differentiation. Furthermore, primary cultures of rat myocard cells were used to examine these same processes during dedifferentiation. In particular, we were interested in the general mechanism that underlies the changes in the supramolecular organisation of titin during in vitro myogenesis. It became obvious that in the differentiating muscle cell cultures the redistribution of desmin, actin and myosin in a typical, differentiation state dependent fashion, always showed a certain delay when compared to titin. The sequence of changes in the assembly of cytoskeletal and sarcomeric structures observed during differentiation of the cell lines was reversed during the process of dedifferentiation in cultured rat myocard cells. These results all indicate that titin is an early marker of myogenic differentiation, both in vivo and in vitro, and the typical reorganisation of this giant molecule is independent of species or muscle cell type.
已建立的不同物种和组织来源的成肌细胞系被用于研究分化过程中肌肉特异性蛋白质的表达和组织。此外,大鼠心肌细胞的原代培养物被用于研究去分化过程中的这些相同过程。特别地,我们对体外肌生成过程中肌联蛋白超分子组织变化的一般机制感兴趣。很明显,在分化的肌肉细胞培养物中,结蛋白、肌动蛋白和肌球蛋白以典型的、依赖分化状态的方式重新分布,与肌联蛋白相比总是表现出一定的延迟。在细胞系分化过程中观察到的细胞骨架和肌节结构组装的变化顺序在培养的大鼠心肌细胞去分化过程中是相反的。这些结果都表明,肌联蛋白在体内和体外都是成肌分化的早期标志物,并且这种巨分子的典型重组与物种或肌肉细胞类型无关。