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Immunosuppressant FK506 induces sustained activation of MAP kinase and promotes neurite outgrowth in PC12 mutant cells incapable of differentiating

机译:免疫抑制剂FK506诱导MAP激酶持续活化并促进无法分化的PC12突变细胞中的神经突向外生长

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摘要

During the continuous culturing of neural PC12 cells, a drug hypersensitive PC12 mutant cell fine (PC12m3) was obtained, which demonstrated high neurite outgrowth when stimulated by various drugs. When the immunosuppressant drug FK506 and nerve growth factor (NGF) were introduced to the PC12m3 cells, the frequency of neurite outgrowth increased approximately 40-fold for NGF alone. However, the effect of FK506 on neuritogenesis in PC12 parental and drug insensitive PC12m1 mutant cells was much lower than in PC12m3 cells. The sustained activation of mitogen-activated protein (MAP) kinase plays an important role in neurite outgrowth of PC12 cells. Interestingly, the drug hypersensitive PC12m3 cells exhibited the sustained activation of MAP kinase with FK506 in comparison to low or no activities in PC12 parental or drug insensitive PC12m1 cells. These results indicate that PC12m3 cells have a novel FK506-induced MAP kinase pathway for neuritogenesis. [References: 26]
机译:在神经PC12细胞的连续培养过程中,获得了药物超敏PC12突变细胞细粒(PC12m3),当受到多种药物刺激时,神经突向外生长。当将免疫抑制剂FK506和神经生长因子(NGF)引入PC12m3细胞时,仅NGF可使神经突生长的频率增加约40倍。但是,FK506对PC12亲本和药物不敏感的PC12m1突变细胞中神经形成的影响远低于PC12m3细胞。丝裂原活化蛋白(MAP)激酶的持续活化在PC12细胞的神经突生长中起重要作用。有趣的是,与PC12亲本或对药物不敏感的PC12m1细胞中的低活性或无活性相比,药物超敏PC12m3细胞表现出FK506对MAP激酶的持续活化作用。这些结果表明,PC12m3细胞具有新型的FK506诱导的MAP激酶通路,用于神经发生。 [参考:26]

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