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首页> 外文期刊>Neuroreport >JNK pathway is required for retinoic acid-induced neurite outgrowth of human neuroblastoma, SH-SY5Y.
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JNK pathway is required for retinoic acid-induced neurite outgrowth of human neuroblastoma, SH-SY5Y.

机译:维甲酸诱导人神经母细胞瘤SH-SY5Y的神经突生长需要JNK通路。

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摘要

Neurite outgrowth is a central event of neuronal differentiation that proceeds in multiple processes requiring various cellular factors. Here we demonstrated that c-Jun N-terminal kinase 1 (JNK1) plays an essential role in RA-induced neurite outgrowth of SH-SY5Y cells. Treatment of SH-SY5Y cells with RA induced a strong activation of JNK1 within 10 min, and the immediate increase of JNK1 activity returned to the basal level in an hour. The second surge of JNK1 activity was observed around 1 day after RA treatment, which coincided with the period of extensive neurite outgrowth. Interestingly, phospho-JNK was concentrated in the nucleus of cells during the early induction, whereas it was distributed into neurite processes during the delayed second activation period. In SH-SY5Y carrying a dominant negative form of SEK1, an upstream kinase of JNK1, both early and late inductions of JNK1 activity were repressed along with RA-induced neurite outgrowth. These results suggest that JNK1 plays an essential role in RA-induced neuronal differentiation of SH-SY5Y cells.
机译:神经突生长是神经元分化的中心事件,其在需要各种细胞因子的多个过程中进行。在这里,我们证明了c-Jun N末端激酶1(JNK1)在RA诱导的SH-SY5Y细胞神经突向外生长中起重要作用。用RA处理SH-SY5Y细胞可在10分钟内诱导JNK1的强烈活化,并且JNK1活性的立即增加在一个小时内恢复到基础水平。在RA治疗后约1天观察到JNK1活性的第二次激增,这与广泛的神经突增生期相吻合。有趣的是,磷酸化-JNK在早期诱导过程中集中在细胞核中,而在延迟的第二个激活期中分布到神经突过程中。在SH-SY5Y带有一个主要的负型SEK1,JNK1的上游激酶,JNK1活性的早期和晚期诱导以及RA诱导的神经突生长均被抑制。这些结果表明,JNK1在RA诱导的SH-SY5Y细胞的神经元分化中起重要作用。

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