TRPM2: a candidate therapeutic target for treating neurological diseases.

TRPM2: a candidate therapeutic target for treating neurological diseases.
复制标题

DOI:
10.1038/aps.2018.31
复制
发表时间:
2018-05
影响因子:
8.2
通讯作者:
Jackson MF
Jackson MF
中科院分区:
医学1区
文献类型:
--
作者:
Belrose JC;Jackson MF

文献摘要

参考文献

被引文献

相似文献

瞬时受体电位 melastatin 2 (TRPM2) 是一种钙 (Ca2+) 渗透性非选择性阳离子通道,属于 TRP 离子通道家族。氧化应激诱导的 TRPM2 激活会引起包括神经元在内的多种细胞类型的异常细胞内 Ca2+ 积累和细胞死亡。 TRPM2 功能异常与多种神经系统疾病有关,包括缺血/中风、阿尔茨海默病、神经性疼痛、帕金森病和双相情感障碍。除了确定 TRPM2 在疾病中的作用的研究之外,在确定 TRPM2 在大脑中的生理功能方面也取得了进展,包括最近的证据表明 TRPM2 对于诱导 N-甲基-D-天冬氨酸 (NMDA) 受体依赖性长期抑郁是必需的,这是谷氨酸突触突触可塑性的一种重要形式。在这里,我们总结了 TRPM2 在中枢神经系统 (CNS) 健康和疾病中作用的最新证据,并讨论了靶向 TRPM2 的潜在治疗意义。总的来说,这些研究表明 TRPM2 代表了神经系统疾病的前瞻性新型治疗靶点。
Transient receptor potential melastatin 2 (TRPM2) is a calcium (Ca2+)-permeable non-selective cation channel belonging to the TRP ion channel family. Oxidative stress-induced TRPM2 activation provokes aberrant intracellular Ca2+ accumulation and cell death in a variety of cell types, including neurons. Aberrant TRPM2 function has been implicated in several neurological disorders including ischemia/stroke, Alzheimer's disease, neuropathic pain, Parkinson's disease and bipolar disorder. In addition to research identifying a role for TRPM2 in disease, progress has been made in the identification of physiological functions of TRPM2 in the brain, including recent evidence that TRPM2 is necessary for the induction of N-methyl-D-aspartate (NMDA) receptor-dependent long-term depression, an important form of synaptic plasticity at glutamate synapses. Here, we summarize recent evidence on the role of TRPM2 in the central nervous system (CNS) in health and disease and discuss the potential therapeutic implications of targeting TRPM2. Collectively, these studies suggest that TRPM2 represents a prospective novel therapeutic target for neurological disorders.
DOI: 10.1038/sj.bjp.0705914
发表时间: 2004-09-01
影响因子: 7.3
作者:
Fonfria, E;Marshall, ICB;McNulty, S
通讯作者: McNulty, S
DOI: 10.1074/jbc.m114.620922
发表时间: 2014-12-26
影响因子: 4.8
作者:
Chen, Shu-jen;Hoffman, Nicholas E.;Miller, Barbara A.
通讯作者: Miller, Barbara A.
DOI: 10.1038/nn1609
发表时间: 2006-01-01
影响因子: 25
作者:
Aoyama, K;Suh, SW;Swanson, RA
通讯作者: Swanson, RA
DOI: 10.1007/s00018-010-0533-1
发表时间: 2011-04
影响因子: 8
作者:
Blenn, C.;Wyrsch, P.;Bader, J.;Bollhalder, M.;Althaus, Felix R.
通讯作者: Althaus, Felix R.
DOI: 10.1085/jgp.200910254
发表时间: 2009-12
期刊: The Journal of general physiology
影响因子: --
作者:
Du J;Xie J;Yue L
通讯作者: Yue L