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p38丝裂原活化蛋白激酶通路在少突胶质细胞增殖和分化过程中调控基因。

p38 Mitogen-Activated Protein Kinase Pathway Regulates Genes during Proliferation and Differentiation in Oligodendrocytes.

作者信息

Haines Jeffery D, Fulton Debra L, Richard Stephane, Almazan Guillermina

机构信息

Department of Pharmacology and Therapeutics, McGill University, 3655 Sir William Osler Promenade, Montreal, Quebec, Canada, H3G 1Y6.

Department of Neurology and Neurosurgery, Montreal Neurological Institute and Hospital, McGill University, 3801 University St, Montreal, Quebec, Canada, H3A 2B4.

出版信息

PLoS One. 2015 Dec 29;10(12):e0145843. doi: 10.1371/journal.pone.0145843. eCollection 2015.

Abstract

We have previously shown that p38 mitogen-activated protein kinase (p38 MAPK) is important for oligodendrocyte (OLG) differentiation and myelination. However, the precise cellular mechanisms by which p38 regulates OLG differentiation remain largely unknown. To determine whether p38 functions in part through transcriptional events in regulating OLG identity, we performed microarray analysis on differentiating oligodendrocyte progenitors (OLPs) treated with a p38 inhibitor. Consistent with a role in OLG differentiation, pharmacological inhibition of p38 down-regulated the transcription of genes that are involved in myelin biogenesis, transcriptional control and cell cycle. Proliferation assays showed that OLPs treated with the p38 inhibitor retained a proliferative capacity which could be induced upon application of mitogens demonstrating that after two days of p38-inhibition OLGs remained poised to continue mitosis. Together, our results suggest that the p38 pathway regulates gene transcription which can coordinate OLG differentiation. Our microarray dataset will provide a useful resource for future studies investigating the molecular mechanisms by which p38 regulates oligodendrocyte differentiation and myelination.

摘要

我们之前已经表明,p38丝裂原活化蛋白激酶(p38 MAPK)对少突胶质细胞(OLG)的分化和髓鞘形成很重要。然而,p38调节OLG分化的确切细胞机制在很大程度上仍然未知。为了确定p38是否部分通过转录事件在调节OLG特性中发挥作用,我们对用p38抑制剂处理的分化少突胶质前体细胞(OLP)进行了微阵列分析。与在OLG分化中的作用一致,p38的药理学抑制下调了参与髓鞘生物合成、转录控制和细胞周期的基因的转录。增殖试验表明,用p38抑制剂处理的OLP保留了增殖能力,在施加有丝分裂原后这种能力可以被诱导,这表明在p38抑制两天后,OLG仍准备好继续有丝分裂。总之,我们的结果表明p38途径调节基因转录,这可以协调OLG分化。我们的微阵列数据集将为未来研究p38调节少突胶质细胞分化和髓鞘形成的分子机制提供有用的资源。

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