Monnier Philippe P, Sierra Ana, Schwab Jan M, Henke-Fahle Sigrid, Mueller Bernhard K
Migragen AG, Spemannstrasse 34, D-72076 Tübingen, Germany.
Mol Cell Neurosci. 2003 Mar;22(3):319-30. doi: 10.1016/s1044-7431(02)00035-0.
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.
轴突在损伤后的中枢神经系统中无法再生。瘢痕中表达的硫酸软骨素蛋白聚糖(CSPG)显著促成了中枢神经系统环境的抑制特性。为了检测CSPG混合物对视网膜神经节细胞(RGC)轴突生长的抑制活性,我们采用了条纹试验和神经纤维生长试验。我们发现,在体外,CSPG施加的抑制作用可被Rho GTP酶的特异性抑制剂C3转移酶或Rho激酶的特异性抑制剂Y27632所阻断。这些结果表明,CSPG相关的神经突生长抑制是由Rho/ROCK信号通路介导的。与这些结果一致,我们发现,分别在存在C3转移酶和Y27632的情况下,视网膜神经节细胞轴突在胶质瘢痕组织上的生长得到了增强。此外,我们表明,最近鉴定出的抑制性CSPG Te38在损伤的脊髓中上调。