Raats J M, Schaart G, Henderik J B, van der Kemp A, Dunia I, Benedetti E L, Pieper F R, Ramaekers F C, Bloemendal H
Department of Biochemistry, University of Nijmegen, The Netherlands.
Eur J Cell Biol. 1996 Nov;71(3):221-36.
To extend our knowledge of the functions of desmin and vimentin intermediate filaments in the developing organism, a construct encoding a truncated desmin subunit driven by the desmin promoter (pDDV), was introduced into the murine germ line. The resulting mutant desmin subunit was assembly-incompetent and capable of disrupting both preexisting desmin and vimentin filaments in a dominant negative fashion in transfected C2C12 muscle cells and in transgenic mouse muscle tissue. Expression of the pDDV was tissue-specific in transgenic mice. High level expression of pDDV occurred in a small percentage of desmin-containing muscle cells. Immunohistochemical staining of muscle tissue showed a diffuse desmin pattern instead of the dots and clumps into which mutant desmin typically accumulates in undifferentiated C2C12 muscle cells in tissue culture. Disruption of the endogenous desmin filaments in Sartorius muscle results in ultrastructural abnormalities.
为了拓展我们对结蛋白和波形蛋白中间丝在发育生物体中功能的认识,将一个由结蛋白启动子驱动的编码截短结蛋白亚基的构建体(pDDV)导入小鼠种系。所产生的突变结蛋白亚基不具备组装能力,并且能够在转染的C2C12肌肉细胞和转基因小鼠肌肉组织中以显性负性方式破坏既有的结蛋白和波形蛋白丝。pDDV在转基因小鼠中的表达具有组织特异性。pDDV在一小部分含结蛋白的肌肉细胞中高水平表达。肌肉组织的免疫组织化学染色显示出弥漫性的结蛋白模式,而不是在组织培养中未分化的C2C12肌肉细胞中突变结蛋白通常聚集形成的点状和团块状。缝匠肌中内源性结蛋白丝的破坏导致超微结构异常。