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以CREB作为潜在靶点的p38丝裂原活化蛋白激酶对少突胶质细胞分化的调控

p38 MAP kinase regulation of oligodendrocyte differentiation with CREB as a potential target.

作者信息

Bhat Narayan R, Zhang Peisheng, Mohanty Sangeeta B

机构信息

Department of Neurosciences, Medical University of South Carolina, 171 Ashley Avenue, Charleston, SC 29425, USA.

出版信息

Neurochem Res. 2007 Feb;32(2):293-302. doi: 10.1007/s11064-006-9274-9. Epub 2007 Jan 19.

Abstract

Despite a substantial understanding of the factors regulating oligodendrocyte differentiation, the signaling mechanisms involved in this process are not well-understood. This study elaborates on the findings (Bhat NR, Zhang P (1997) FASEB J 11:A925; Baron W, Metz B, Bansal R, Hoekstra D, de Vries H (2000) Mol Cell Neurosci 15:314-329) of a role for p38 MAP kinase signaling in oligodendrocyte differentiation and myelin gene expression. When proliferating oligodendrocyte progenitors were switched to a growth factor-free differentiation medium, there was a rapid activation of p38 kinase that correlated with an increased phosphorylation of CREB, a down-stream target and a factor involved in oligodendrocyte differentiation. Addition of forskolin, a known inducer of intracellular c-AMP and of oligodendrocyte differentiation, also stimulated CREB phosphorylation in a p38 kinase dependent way. Pharmacological inhibition of p38 interfered with the morphological and antigenic changes associated with differentiating oligodendrocytes as well as with the developmental and forskolin-induced expression of myelin basic protein, thereby supporting an essential role for p38 MAPK pathway in oligodendrocyte differentiation.

摘要

尽管对调节少突胶质细胞分化的因素已有相当多的了解,但该过程中涉及的信号传导机制仍未得到充分理解。本研究详细阐述了p38丝裂原活化蛋白激酶(MAPK)信号传导在少突胶质细胞分化和髓鞘基因表达中的作用这一研究结果(Bhat NR,Zhang P(1997年)《美国实验生物学会联合会杂志》11:A925;Baron W,Metz B,Bansal R,Hoekstra D,de Vries H(2000年)《分子与细胞神经科学》15:314 - 329)。当增殖的少突胶质前体细胞转换至无生长因子的分化培养基时,p38激酶迅速激活,这与下游靶点CREB(一种参与少突胶质细胞分化的因子)磷酸化增加相关。添加福斯可林(一种已知的细胞内c - AMP诱导剂和少突胶质细胞分化诱导剂)也以p38激酶依赖的方式刺激CREB磷酸化。p38的药理学抑制干扰了与分化中的少突胶质细胞相关的形态学和抗原性变化,以及髓鞘碱性蛋白的发育性和福斯可林诱导性表达,从而支持p38 MAPK通路在少突胶质细胞分化中起关键作用。

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