Abe M, Saitoh O, Nakata H, Yoda A, Matsuda R
Department of Biology, The University of Tokyo, Meguro-ku, Japan.
Exp Cell Res. 1996 Nov 25;229(1):48-59. doi: 10.1006/excr.1996.0342.
Expression of neurofilament proteins, NF140K, NF68K, and NF200K, in C2C12 mouse skeletal muscle cells was studied. Immunofluorescence and immunoblot analyses revealed that NF140K was expressed in proliferating C2C12 cells and its localization was similar to desmin, a muscle-specific intermediate filament protein. NF140K became undetectable in C2C12 cells as muscle cell differentiation proceeded. Reverse transcription-polymerase chain reaction (RT-PCR) and Northern blot analyses confirmed the expression of NF140K, NF68K, and NF200K in proliferating C2C12 cells. Sequences of the RT-PCR products of NF140K and NF68K were identical to that of authentic mouse NF140K and NF68K, respectively. The NF140K and NF68K mRNA were down-regulated during myogenesis in contrast to the up-regulation of mRNA encoding troponin-T. Furthermore, subcloned C2C12 cells, which express NF140K at a higher level, exhibited retarded myogenesis, i.e., delayed onset of myosin heavy chain synthesis and myoblast fusion. These results suggest that neurofilament proteins may play an inhibitory role in commitment of muscle cell differentiation. The presence of neurofilament proteins in skeletal muscle cells indicates that desmin, vimentin, and neurofilament proteins can be expressed in a single muscle cell.
研究了神经丝蛋白NF140K、NF68K和NF200K在C2C12小鼠骨骼肌细胞中的表达。免疫荧光和免疫印迹分析显示,NF140K在增殖的C2C12细胞中表达,其定位与结蛋白(一种肌肉特异性中间丝蛋白)相似。随着肌肉细胞分化的进行,NF140K在C2C12细胞中变得无法检测到。逆转录-聚合酶链反应(RT-PCR)和Northern印迹分析证实了NF140K、NF68K和NF200K在增殖的C2C12细胞中的表达。NF140K和NF68K的RT-PCR产物序列分别与正宗小鼠NF140K和NF68K的序列相同。与肌钙蛋白-T编码mRNA的上调相反,NF140K和NF68K mRNA在肌生成过程中下调。此外,更高水平表达NF140K的亚克隆C2C12细胞表现出延迟的肌生成,即肌球蛋白重链合成和成肌细胞融合的起始延迟。这些结果表明神经丝蛋白可能在肌肉细胞分化的定向中起抑制作用。骨骼肌细胞中神经丝蛋白的存在表明结蛋白、波形蛋白和神经丝蛋白可以在单个肌肉细胞中表达。