Chemical inhibitors of cyclin-dependent kinases control proliferation, apoptosis and differentiation of oligodendroglial cells

被引:8
作者
Nguyen, L
Malgrange, B
Rocher, V
Hans, G
Moonen, G
Rigo, JM
Belachew, S
机构
[1] Univ Liege, Ctr Cellular & Mol Neurobiol, B-4020 Liege, Belgium
[2] Univ Liege, CHU Sart Tilman, Dept Neurol, B-4000 Liege, Belgium
关键词
roscovitine; cell cycle; oligodendroglia; differentiation; apoptosis; rat cerebral cortex;
D O I
10.1016/S0736-5748(03)00075-3
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Since cyclin-dependent kinases (Cdks) and their endogenous inhibitors (Cdkis) play an essential role as regulators of cell cycle withdrawal and onset of differentiation within oligodendroglial cells, we assessed here the effects of exogenous chemical Cdk inhibitors (CKIs) on cultured rat cortical oligodendrocyte progenitor cells (OPCs). We showed that purine derivatives and especially roscovitine strongly inhibited OPCs proliferation. In the presence of mitogenic signals, roscovitine synergized with thyroid hormone to stimulate oligodendrocyte differentiation. Roscovitine also prevented oligodendroglial apoptosis induced by growth factor deprivation. We thus demonstrated that small molecular weight chemical CKIs have important effects on crucial events of oligodendroglial development in vitro. This might open prospects for using these apparently well tolerated agents in remyelination strategies. (C) 2003 ISDN. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:321 / 326
页数:6
相关论文
共 25 条
[1]  
AvellanaAdalid V, 1996, J NEUROSCI RES, V45, P558, DOI 10.1002/(SICI)1097-4547(19960901)45:5<558::AID-JNR6>3.0.CO
[2]  
2-B
[3]  
Belachew S, 2002, J NEUROSCI, V22, P8553
[4]   Glycine triggers an intracellular calcium influx in oligodendrocyte progenitor cells which is mediated by the activation of both the ionotropic glycine receptor and Na+ -: dependent transporters [J].
Belachew, S ;
Malgrange, B ;
Rigo, JM ;
Rogister, B ;
Leprince, P ;
Hans, G ;
Nguyen, L ;
Moonen, G .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2000, 12 (06) :1924-1930
[5]  
Casaccia-Bonnefil P, 2000, GLIA, V29, P124, DOI 10.1002/(SICI)1098-1136(20000115)29:2<124::AID-GLIA5>3.0.CO
[6]  
2-O
[7]  
Durand B, 2000, BIOESSAYS, V22, P64
[8]   Progression from extrinsic to intrinsic signaling in cell fate specification: A view from the nervous system [J].
Edlund, T ;
Jessell, TM .
CELL, 1999, 96 (02) :211-224
[9]  
Ghiani CA, 1999, DEVELOPMENT, V126, P1077
[10]  
Ghiani CA, 2001, J NEUROSCI, V21, P1274