p75神经营养因子受体的逆行凋亡信号。

Q4 Neuroscience Neuronal signaling Pub Date : 2017-02-24 eCollection Date: 2017-02-01 DOI:10.1042/NS20160007
Amrita Pathak, Bruce D Carter
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引用次数: 8

摘要

神经营养因子是哺乳动物神经系统发育和维持所必需的靶源因子。它们通常由神经元靶组织产生,并与轴突末梢的受体相互作用。因此,局部产生的神经营养因子信号必须从轴突传递回细胞体。神经营养因子结合Trk受体的逆行生存信号已被广泛研究。然而,神经营养因子也与p75受体结合,可在多种情况下诱导细胞凋亡。在远端轴突末端选择性激活p75已被证明产生逆行凋亡信号,尽管所涉及的机制尚不清楚。本文综述了逆行促凋亡信号传导的现有证据,特别是p75受体的作用,并讨论了该领域尚未解决的问题。深入了解逆行凋亡信号传导的机制对于理解许多疾病和损伤中神经退行性变的病因至关重要。
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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Retrograde apoptotic signaling by the p75 neurotrophin receptor.

Neurotrophins are target-derived factors necessary for mammalian nervous system development and maintenance. They are typically produced by neuronal target tissues and interact with their receptors at axonal endings. Therefore, locally generated neurotrophin signals must be conveyed from the axon back to the cell soma. Retrograde survival signaling by neurotrophin binding to Trk receptors has been extensively studied. However, neurotrophins also bind to the p75 receptor, which can induce apoptosis in a variety of contexts. Selective activation of p75 at distal axon ends has been shown to generate a retrograde apoptotic signal, although the mechanisms involved are poorly understood. The present review summarizes the available evidence for retrograde proapoptotic signaling in general and the role of the p75 receptor in particular, with discussion of unanswered questions in the field. In-depth knowledge of the mechanisms of retrograde apoptotic signaling is essential for understanding the etiology of neurodegeneration in many diseases and injuries.

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来源期刊
CiteScore
4.60
自引率
0.00%
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0
审稿时长
14 weeks
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