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成肌调节因子在C2C12细胞系融合过程中的作用

Involvement of myogenic regulator factors during fusion in the cell line C2C12.

作者信息

Dedieu Stéphane, Mazères Germain, Cottin Patrick, Brustis Jean-Jacques

机构信息

ISTAB-USC-INRA 429, Laboratoire de Biochimie et Technologie des Aliments, Université Bordeaux I, Talence, France.

出版信息

Int J Dev Biol. 2002 Mar;46(2):235-41.

Abstract

The myogenic factors, MyoD, myogenin, Myf5 and MRF4, can activate skeletal muscle differentiation when overexpressed in non-muscular cells. Gene targeting experiments have provided much insight into the in vivo functions of MRF and have defined two functional groups of MRFs. MyoD and Myf5 may be necessary for myoblast determination while myogenin and MRF4 may be required later during differentiation. However, the specific role of these myogenic factors has not been clearly defined during one important stage of myogenesis: the fusion of myoblasts. Using cultured C2C12 mouse muscular cells, the time-course of these proteins was analyzed and a distinct expression pattern in fusing cells was revealed. In an attempt to clarify the role of each of these regulators during myoblast fusion, an antisense strategy using oligonucleotides with phosphorothioate backbone modification was adoped. The results showed that the inhibition of myogenin and Myf5 activity is capable of significantly preventing fusion. Furthermore, the inhibition of MyoD can wholly arrest the engaged fusion process in spite of high endogenous expression of both myogenin and Myf5. Consequently, each MRF seems to have, at this defined step of myogenesis, a specific set of functions that can not be substituted for by the others and therefore may regulate a distinct subset of muscle-specific genes at the onset of fusion.

摘要

生肌因子MyoD、肌细胞生成素、Myf5和MRF4在非肌肉细胞中过表达时可激活骨骼肌分化。基因靶向实验为MRF的体内功能提供了很多见解,并确定了MRF的两个功能组。成肌细胞的确定可能需要MyoD和Myf5,而分化后期可能需要肌细胞生成素和MRF4。然而,在肌生成的一个重要阶段——成肌细胞融合过程中,这些生肌因子的具体作用尚未明确界定。利用培养的C2C12小鼠肌肉细胞,分析了这些蛋白质的时间进程,并揭示了融合细胞中独特的表达模式。为了阐明这些调节因子在成肌细胞融合过程中的各自作用,采用了一种使用具有硫代磷酸酯主链修饰的寡核苷酸的反义策略。结果表明,抑制肌细胞生成素和Myf5的活性能够显著阻止融合。此外,尽管肌细胞生成素和Myf5的内源性表达水平很高,但抑制MyoD可完全阻止正在进行的融合过程。因此,在这个确定的肌生成步骤中,每个MRF似乎都有一组特定的功能,这些功能不能被其他因子替代,因此可能在融合开始时调节不同的肌肉特异性基因子集。

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