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瞬时受体电位通道与程序性细胞死亡

TRPC Channels and Programmed Cell Death.

作者信息

Zhou Jian, Jia Yichang

机构信息

Laboratory of Neural Signal Transduction, Institute of Neuroscience, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, 320 Yueyang Road, Shanghai, 200031, China.

School of Medicine, Tsinghua University, Medical Science Building, Room D204, Beijing, 100084, China.

出版信息

Adv Exp Med Biol. 2017;976:47-60. doi: 10.1007/978-94-024-1088-4_5.

Abstract

Neurotrophins, including nerve growth factor (NGF) and brain-derived neurotrophic factor (BDNF), bind to their high-affinity receptors to promote neuronal survival during brain development. One of the key downstream pathways is the phospholipase C (PLC) pathway, which not only plays a central role in calcium release from internal store but also in activation of TRPC channels coupled with neurotrophin receptors. TRPC channels are required for the neurotrophin-mediated neuronal protective effects. In addition, activation of TRPC channels is able to protect neurons in the absence of neurotrophin. In some circumstances, TRPC channels coupled with metabotropic glutamate receptor may mediate the excitotoxicity by calcium overload. One of the key questions in the field is the channel gating mechanisms; understanding of which would help design compounds to modulate the channel properties. The development and identification of TRPC channel agonists or blockers are promising and may unveil new therapeutic drugs for the treatment of neurodegenerative diseases and epilepsy.

摘要

神经营养因子,包括神经生长因子(NGF)和脑源性神经营养因子(BDNF),与它们的高亲和力受体结合,以促进大脑发育过程中的神经元存活。关键的下游途径之一是磷脂酶C(PLC)途径,它不仅在从内部储存释放钙方面起核心作用,而且在与神经营养因子受体偶联的瞬时受体电位阳离子通道(TRPC)通道的激活中也起核心作用。TRPC通道是神经营养因子介导的神经元保护作用所必需的。此外,在没有神经营养因子的情况下,TRPC通道的激活能够保护神经元。在某些情况下,与代谢型谷氨酸受体偶联的TRPC通道可能通过钙超载介导兴奋性毒性。该领域的关键问题之一是通道门控机制;对其的理解将有助于设计调节通道特性的化合物。TRPC通道激动剂或阻滞剂的开发和鉴定前景广阔,可能会揭示用于治疗神经退行性疾病和癫痫的新治疗药物。

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