C2C12型
肌发生
细胞融合
CD81号
合胞体
心肌细胞
细胞生物学
跨膜蛋白
生物
融合蛋白
细胞
骨骼肌
免疫球蛋白超家族
分子生物学
免疫学
生物化学
细胞粘附分子
受体
重组DNA
解剖
病毒
基因
丙型肝炎病毒
作者
Isao Tachibana,Martin E. Hemler
标识
DOI:10.1083/jcb.146.4.893
摘要
The role of transmembrane 4 superfamily (TM4SF) proteins during muscle cell fusion has not been investigated previously. Here we show that the appearance of TM4SF protein, CD9, and the formation of CD9–β1 integrin complexes were both regulated in coordination with murine C2C12 myoblast cell differentiation. Also, anti-CD9 and anti-CD81 monoclonal antibodies substantially inhibited and delayed conversion of C2C12 cells to elongated myotubes, without affecting muscle-specific protein expression. Studies of the human myoblast-derived RD sarcoma cell line further demonstrated that TM4SF proteins have a role during muscle cell fusion. Ectopic expression of CD9 caused a four- to eightfold increase in RD cell syncytia formation, whereas anti-CD9 and anti-CD81 antibodies markedly delayed RD syncytia formation. Finally, anti-CD9 and anti-CD81 monoclonal antibodies triggered apoptotic degeneration of C2C12 cell myotubes after they were formed. In summary, TM4SF proteins such as CD9 and CD81 appear to promote muscle cell fusion and support myotube maintenance.
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