The Rho/ROCK pathway mediates neurite growth-inhibitory activity associated with the chondroitin sulfate proteoglycans of the CNS glial scar

被引:360
作者
Monnier, PP
Sierra, A
Schwab, JM
Henke-Fahle, S
Mueller, BK
机构
[1] Migragen AG, D-72076 Tubingen, Germany
[2] Univ Tubingen, Dept Ophthalmol, D-72076 Tubingen, Germany
关键词
D O I
10.1016/S1044-7431(02)00035-0
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Axons fail to regenerate in the central nervous system after injury. Chondroitin sulfate proteoglycans (CSPG) expressed in the scar significantly contribute to the nonpermissive properties of the central nervous system environment. To examine the inhibitory activity of a CSPG mixture on retina ganglion cell (RGC) axon growth, we employed both a stripe assay and a nerve fiber outgrowth assay. We show that the inhibition exerted by CSPGs in vitro can be blocked by application of either C3 transferase, a specific inhibitor of the Rho GTPase, or Y27632, a specific inhibitor of the Rho kinase. These results demonstrate that CSPG-associated inhibition of neurite outgrowth is mediated by the Rho/ROCK signaling pathway. Consistent with these results, we found that retina ganglion cell axon growth on glial scar tissue was enhanced in the presence of C3 transferase and Y27632, respectively. In addition, we show that the recently identified inhibitory CSPG Te38 is upregulated in the lesioned spinal cord. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:319 / 330
页数:12
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