Matsuda R, Abe M
Department of Life Sciences, University of Tokyo, Japan.
Cell Struct Funct. 1997 Feb;22(1):117-21. doi: 10.1247/csf.22.117.
Expression of neurofilament 140K protein in C2C12 mouse skeletal muscle cells was studied. Immunofluorescence and immunoblot analyses revealed that NF140K was expressed at the proliferative stage and was colocalized with the muscle-specific intermediate protein desmin. As muscle cell differentiation proceeded, the number of NF140K-positive cells decreased whereas the number of cells expressing muscle-specific marker proteins such as sarcomeric myosin heavy chain and troponin-T increased. Down-regulation of NF140K and upregulation of a myogenic regulatory gene, the myogenin gene, started simultaneously. In differentiated muscle cell cultures, unfused cells residing between myotubes remained NF140K-positive. NF140K and desmin double-positive cells were also found in a primary culture of adult mouse skeletal muscle cells. The results suggest that NF140K may be a unique marker for uncommitted myoblasts.
研究了神经丝140K蛋白在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在增殖阶段表达,并与肌肉特异性中间蛋白结蛋白共定位。随着肌肉细胞分化的进行,NF140K阳性细胞数量减少,而表达肌节肌球蛋白重链和肌钙蛋白-T等肌肉特异性标记蛋白的细胞数量增加。NF140K的下调和生肌调节基因肌细胞生成素基因的上调同时开始。在分化的肌肉细胞培养物中,位于肌管之间的未融合细胞仍为NF140K阳性。在成年小鼠骨骼肌细胞的原代培养物中也发现了NF140K和结蛋白双阳性细胞。结果表明,NF140K可能是未分化成肌细胞的独特标志物。