TRPC Channels and Programmed Cell Death

被引:6
作者
Zhou, Jian [1 ]
Jia, Yichang [2 ,3 ,4 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Biol Sci, Inst Neurosci, Lab Neural Signal Transduct, 320 Yueyang Rd, Shanghai 200031, Peoples R China
[2] Tsinghua Univ, Sch Med, Med Sci Bldg,Room D204, Beijing 100084, Peoples R China
[3] Peking Tsinghua Joint Ctr Life Sci, Beijing 100084, Peoples R China
[4] IDG McGovern Inst Brain Res Tsinghua, Beijing 100084, Peoples R China
来源
TRANSIENT RECEPTOR POTENTIAL CANONICAL CHANNELS AND BRAIN DISEASES | 2017年 / 976卷
关键词
TRPC channels; Neurotrophins; Programmed cell death; EPIDERMAL-GROWTH-FACTOR; RECEPTOR POTENTIAL CHANNELS; NEUROTROPHIC FACTOR; CATION CHANNEL; NERVOUS-SYSTEM; DOPAMINERGIC-NEURONS; CRYSTAL-STRUCTURE; CA2+ ENTRY; BRAIN; KINASE;
D O I
10.1007/978-94-024-1088-4_5
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
引用
收藏
页码:47 / 60
页数:14
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