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Involvement of c-Jun N-terminal kinase activities in skeletal muscle differentiation

机译:c-Jun N-末端激酶活性与骨骼肌分化有关

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摘要

Previous studies on skeletal muscle differentiation showed that myogenesis is regulated by extracellular signal-regulated kinases (ERK-1/-2) and p38 mitogen activated kinase (MAPK) pathways. Present study shows that c-Jun NH(2)-terminal protein kinase (JNK) activities were up regulated during skeletal muscle differentiation in rat skeletal muscle L6E9 cells, as determined by Western immunoblot of differentiating cells probed with anti-phospho-JNK antibody. Inhibition of JNK activities by JNK inhibitor II drastically inhibited differentiation as determined by decreased myosin, myogenin expression and creatine kinase activity. The inhibition of the differentiation was regulated by apoptosis as determined by the detection of poly(ADP-ribose) polymerase (PARP) cleavage, terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling (TUNEL) positive cells when JNK activities were inhibited. Apoptosis was accompanied by marked expression and activation of c-Jun and p53 transcription factors. Taken together, our results indicate that basal JNK activities are essential for regulating skeletal muscle differentiation, and inhibition of JNK activation affects myogenesis by apoptosis dependent on c-Jun and p53 transcription factors.
机译:以前对骨骼肌分化的研究表明,肌细胞的生成受细胞外信号调节激酶(ERK-1 / -2)和p38丝裂原活化激酶(MAPK)通路的调节。目前的研究表明,c-Jun NH(2)末端蛋白激酶(JNK)的活性在大鼠骨骼肌L6E9细胞的骨骼肌分化过程中被上调,这是通过用抗磷酸JNK抗体探测的分化细胞的Western免疫印迹法确定的。通过降低肌球蛋白,肌生成素表达和肌酸激酶活性来确定,JNK抑制剂II对JNK活性的抑制作用极大地抑制了分化。当抑制JNK活性时,通过检测多聚(ADP-核糖)聚合酶(PARP)裂解,末端脱氧核苷酸转移酶介导的dUTP缺口末端标记(TUNEL)阳性细胞来确定凋亡,从而调节分化的抑制作用。凋亡伴随着c-Jun和p53转录因子的明显表达和激活。两者合计,我们的结果表明,基础的JNK活性对于调节骨骼肌的分化是必不可少的,并且抑制JNK活化会通过依赖c-Jun和p53转录因子的细胞凋亡影响肌发生。

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  • 来源
    《Journal of Muscle Research and Cell Motility》 |2004年第8期|645-655|共11页
  • 作者单位

    Signal Transduction Research Laboratory Department of Biotechnology National Institute of Pharmaceutical Education and ResearchMount Sinai School of Medicine Department of Oncological Sciences Icahn Medical Institute;

    Signal Transduction Research Laboratory Department of Biotechnology National Institute of Pharmaceutical Education and Research;

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