Receptors in neurodegenerative diseases

Wolfgang Froestl
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引用次数: 6

Abstract

The ability of trophic factors to regulate developmental neuronal survival and adult nervous system plasticity suggests the use of these molecules to treat neurodegeneration associated with human diseases, such as Alzheimer's, Huntington's and Parkinson's disease, of amyotrophic lateral sclerosis and peripheral sensory neuropathies. Recent biological data on the neutrotrophins NGF and BDNF, on GDNF, CNTF and IGF-I are discussed together with first results from clinical trials. Literature is presented on the three-dimensional structures of these trophic factors and on models proposed for ligand–receptor interactions. Substantial progress has been made in the understanding of the mechanisms of apoptosis. The cascade consisting of interaction of apoptosis-inducing ligands with death receptors, the coupling of this complex to adaptor proteins via death domains, the further recruitment of procaspases via death effector or caspase recruitment domains and the execution of cell death via the effector caspases is briefly outlined.

神经退行性疾病中的受体
营养因子调节发育性神经元存活和成人神经系统可塑性的能力表明,这些分子可用于治疗与人类疾病相关的神经变性,如阿尔茨海默氏症、亨廷顿氏病和帕金森病、肌萎缩侧索硬化症和周围感觉神经病变。本文讨论了中性粒细胞NGF和BDNF、GDNF、CNTF和IGF-I的最新生物学数据以及临床试验的初步结果。文献介绍了这些营养因子的三维结构和提出的配体-受体相互作用的模型。对细胞凋亡机制的认识已取得实质性进展。该级联包括凋亡诱导配体与死亡受体的相互作用,该复合物通过死亡结构域与衔接蛋白的偶联,通过死亡效应或半胱天冬酶募集结构域进一步募集原半胱天冬酶,以及通过效应半胱天冬酶执行细胞死亡。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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