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首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >Repulsion of cerebellar granule neurons by chondroitin sulfate proteoglycans is mediated by MAPK pathway.
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Repulsion of cerebellar granule neurons by chondroitin sulfate proteoglycans is mediated by MAPK pathway.

机译:硫酸软骨素蛋白聚糖对小脑颗粒神经元的排斥作用是由MAPK途径介导的。

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摘要

Inhibitory molecules associated with myelin and glial scar formation inhibit axon regeneration after an injury to the central nervous system (CNS). Chondroitin sulfate proteoglycans (CSPGs) that are expressed in the scar contribute to the non-permissive properties of the CNS environment. Here, we employed a spot substrate assay and demonstrated that CSPGs have a repulsive effect on cell bodies as well as neurites of the postnatal cerebellar granule neurons (CGNs) in vitro. Through a brief inhibitor screen, we observed that the effects of CSPGs were abolished in the presence of mitogen-activated protein kinase (MAPK) inhibitor or epidermal growth factor receptor (EGFR) inhibitor. The MAPK pathway was activated in the neurons treated with CSPGs, and this activation was dependent on EGFR. Thus, CSPGs triggered the inhibition of CGNs through the activation of the EGFR-mediated MAPK pathway.
机译:与髓磷脂和神经胶质瘢痕形成相关的抑制分子抑制中枢神经系统(CNS)损伤后的轴突再生。瘢痕中表达的硫酸软骨素蛋白聚糖(CSPG)导致CNS环境的非许可性质。在这里,我们采用了斑点底物测定法,并证明了CSPG在体外对细胞体以及产后小脑颗粒神经元(CGN)的神经突具有排斥作用。通过简短的抑制剂筛选,我们观察到在有丝分裂原激活的蛋白激酶(MAPK)抑制剂或表皮生长因子受体(EGFR)抑制剂的存在下,CSPG的作用被消除。在用CSPGs处理的神经元中,MAPK通路被激活,这种激活取决于EGFR。因此,CSPG通过激活EGFR介导的MAPK途径来触发CGN的抑制。

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