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使用SB202190和SB203580抑制p38丝裂原活化蛋白激酶诱导培养的成熟少突胶质细胞凋亡。

Inhibition of p38 mitogen-activated protein kinase-induced apoptosis in cultured mature oligodendrocytes using SB202190 and SB203580.

作者信息

Hamanoue Makoto, Sato Kenichiro, Takamatsu Ken

机构信息

Department of Physiology, Toho University School of Medicine, 5-21-16 Ohmori-nishi, Tokyo 143-8540, Japan.

出版信息

Neurochem Int. 2007 Jul;51(1):16-24. doi: 10.1016/j.neuint.2007.03.005. Epub 2007 Mar 21.

Abstract

p38 Mitogen-activated protein kinase (p38 MAPK) is expressed in the oligodendrocyte lineage, and its activity has been implicated in the proliferation and transition of early progenitors into late progenitors. Although p38 MAPK expression has been found in the myelin sheath, however, its role in mature oligodendrocytes remains unknown. In the present study, in order to address the role of p38 MAPK in mature oligodendrocytes, selective inhibitors of p38 MAPK, SB202190, and SB203580 were added to primary cultures of mature oligodendrocytes. After 24h of exposure to the inhibitors, the appearance, and number of A2B5-positive progenitors were unchanged. However, the 2',3'-cyclic nucleotide-3'-phosphohydrolase-positive mature oligodendrocytes disappeared, and the numbers of living cells decreased in comparison to the control cells treated with SB202474, a negative analog of SB203580. Increases in the number of terminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling-positive nuclei and in the activity of caspase-3/7 were detected 16 h after exposure to the inhibitors, thus causing the mature oligodendrocytes to die due to apoptosis. Similar results were obtained using a differentiated rat oligodendrocyte precursor cell (OPC) line, central glia-4 (CG-4). These findings indicate that p38 MAPK is vital for mature oligodendrocyte survival.

摘要

p38丝裂原活化蛋白激酶(p38 MAPK)在少突胶质细胞谱系中表达,其活性与早期祖细胞向晚期祖细胞的增殖和转变有关。然而,尽管已在髓鞘中发现p38 MAPK的表达,但其在成熟少突胶质细胞中的作用仍不清楚。在本研究中,为了探讨p38 MAPK在成熟少突胶质细胞中的作用,将p38 MAPK的选择性抑制剂SB202190和SB203580添加到成熟少突胶质细胞的原代培养物中。在暴露于抑制剂24小时后,A2B5阳性祖细胞的外观和数量没有变化。然而,2',3'-环核苷酸-3'-磷酸水解酶阳性的成熟少突胶质细胞消失了,与用SB203580的阴性类似物SB202474处理的对照细胞相比,活细胞数量减少。在暴露于抑制剂16小时后,检测到末端脱氧核苷酸转移酶介导的dUTP缺口末端标记阳性细胞核数量增加以及caspase-3/7活性增加,从而导致成熟少突胶质细胞因凋亡而死亡。使用分化的大鼠少突胶质前体细胞(OPC)系中枢神经胶质-4(CG-4)也获得了类似的结果。这些发现表明p38 MAPK对成熟少突胶质细胞的存活至关重要。

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