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The Nogo66 receptor pathway and CNS axon regeneration: new hopes for treating CNS injuries and neurodegeneration

机译:Nogo66受体途径与中枢神经系统轴突再生:治疗中枢神经系统损伤和神经变性的新希望

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摘要

The neuronal leucine-rich repeat Nogo66 receptor (NgR) interacts with the myelin proteins Nogo66, myelin associated glycoprotein and oligodendro-cyte myelin glycoprotein to inhibit axon growth. Modulation of these cell surface NgR-dependent interactions or the inhibitory intracellular signalling pathways may promote axon growth in the CNS after injury and present an attractive axon regeneration platform for treating CNS injuries or even neu-rodegenerative disorders. Multiple NgR antagonism approaches, including soluble NgR proteins, anti-NgR antibodies, a Nogo-derived antagonist peptide and NgR signal transduction modulators, have demonstrated striking efficacies in promoting functional recoveries in animal models of spinal cord injury, stroke and multiple sclerosis. This review summarises the neurobiology of the NgR pathway and the various drug discovery strategies that are specifically based on modulation of the myelin-NgR interaction.
机译:富含亮氨酸的神经元重复Nogo66受体(NgR)与髓磷脂蛋白Nogo66,髓磷脂相关糖蛋白和少突胶质细胞髓磷脂糖蛋白相互作用,以抑制轴突生长。这些细胞表面依赖NgR的相互作用或抑制性细胞内信号传导途径的调节可促进损伤后中枢神经系统中轴突的生长,并呈现出有吸引力的轴突再生平台,用于治疗中枢神经系统损伤甚至神经退行性疾病。多种NgR拮抗方法,包括可溶性NgR蛋白,抗NgR抗体,Nogo衍生的拮抗剂肽和NgR信号转导调节剂,在促进脊髓损伤,中风和多发性硬化的动物模型中的功能恢复方面显示出惊人的功效。这篇综述总结了NgR途径的神经生物学和各种药物发现策略,这些策略特别基于对髓磷脂-NgR相互作用的调节。

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