Miller J B
Cecil B. Day Laboratory for Neuromuscular Research, Massachusetts General Hospital, Charlestown 02129.
J Cell Biol. 1990 Sep;111(3):1149-59. doi: 10.1083/jcb.111.3.1149.
Different mouse muscle cell lines were found to express distinct patterns of myosin heavy chain (MHC) isoforms, MyoD1, and myogenin, but there appeared to be no correlation between the pattern of MHC expression and the patterns of MyoD1 and myogenin expression. Myogenic cell lines were generated from unconverted C3H10T1/2 cells by 5-azacytidine treatment (Aza cell lines) and by stable transfection with MyoD1 (TD cell lines) or myogenin (TG cell lines). Myogenic differentiation of the newly generated cell lines was compared to that of the C2C12 and BC3H-1 cell lines. Immunoblot analysis showed that differentiated cells of each line expressed the embryonic and slow skeletal/beta-cardiac MHC isoforms though slow MHC was expressed at a much lower, barely detectable level in BC3H-1 cells. Differentiated cells of each line except BC3H-1 also expressed an additional MHC(s) that was probably the perinatal MHC isoform. Myogenin mRNA was expressed by every cell line, and, with the exception of BC3H-1 (cf., Davis, R. L., H. Weintraub, and A. B. Lassar. 1987. Cell. 51:987-1000), MyoD1 mRNA was expressed by every cell line. To determine if MyoD1 expression would alter the differentiation of BC3H-1 cells, cell lines (termed BD) were generated by transfecting BC3H-1 cells with MyoD1 under control of the beta-actin promoter. The MyoD1 protein expressed in BD cells was correctly localized in the nucleus, and, unlike the parental BC3H-1 cell line that formed differentiated MHC-expressing cells, which were predominantly mononucleated, BD cell lines formed long, multinucleated myotubes (cf., Brennan, T. J., D. G. Edmondson, and E. N. Olson. 1990. J. Cell. Biol. 110:929-938). Despite the differences in morphology and MyoD1 expression, BD myotubes and the parent BC3H-1 cells expressed the same pattern of sarcomeric MHCs.
研究发现,不同的小鼠肌肉细胞系表达不同模式的肌球蛋白重链(MHC)异构体、肌分化决定因子1(MyoD1)和成肌素,但MHC的表达模式与MyoD1和成肌素的表达模式之间似乎没有相关性。通过5-氮杂胞苷处理(Aza细胞系)以及用MyoD1(TD细胞系)或成肌素(TG细胞系)进行稳定转染,从未转化 的C3H10T1/2细胞中生成了成肌细胞系。将新生成的细胞系的成肌分化与C2C12和BC3H-1细胞系的成肌分化进行了比较。免疫印迹分析表明,每个细胞系的分化细胞都表达胚胎型和慢肌/β-心肌MHC异构体,不过慢肌MHC在BC3H-1细胞中的表达水平要低得多,几乎检测不到。除BC3H-1外,每个细胞系的分化细胞还表达了一种额外的MHC,可能是围生期MHC异构体。每个细胞系都表达成肌素mRNA,除了BC3H-1(参见Davis, R. L., H. Weintraub, and A. B. Lassar. 1987. Cell. 51:987 - 1000),每个细胞系都表达MyoD1 mRNA。为了确定MyoD1的表达是否会改变BC3H-1细胞的分化,通过在β-肌动蛋白启动子的控制下用MyoD1转染BC3H-1细胞,生成了细胞系(称为BD)。BD细胞中表达的MyoD1蛋白正确定位于细胞核,与亲代BC3H-1细胞系不同,亲代BC3H-1细胞系形成的分化的MHC表达细胞主要是单核的,而BD细胞系形成了长的、多核的肌管(参见Brennan, T. J., D. G. Edmondson, and E. N. Olson. 1990. J. Cell. Biol. 110:929 - 938)。尽管在形态和MyoD1表达上存在差异,但BD肌管和亲代BC3H-1细胞表达相同模式的肌节MHC。