Acidosis, Acid-Sensing Ion Channels, and Neuronal Cell Death

被引:51
作者
Wang, Yi-Zhi [1 ,2 ,3 ]
Xu, Tian-Le [1 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Med, Div Neurosci, Dept Biochem & Mol Cell Biol,Inst Med Sci, Shanghai 200025, Peoples R China
[2] Chinese Acad Sci, Inst Neurosci, Shanghai 200031, Peoples R China
[3] Chinese Acad Sci, State Key Lab Neurosci, Shanghai Inst Biol Sci, Shanghai 200031, Peoples R China
基金
中国国家自然科学基金;
关键词
Acidosis; ASIC1a; Neuronal cell death; Spermine; Ischemic stroke; EXTRACELLULAR ACIDOSIS; H-1-NMR SPECTROSCOPY; HUNTINGTONS-DISEASE; SYNAPTIC-TRANSMISSION; SPREADING DEPRESSION; HIPPOCAMPAL-NEURONS; PARKINSONS-DISEASE; ALZHEIMERS-DISEASE; ENDOTHELIAL-CELLS; GABA(A) RECEPTORS;
D O I
10.1007/s12035-011-8204-2
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Acidosis is a common feature of many neuronal diseases and often accompanied with adverse consequences such as pain and neuronal injury. Before the discovery of acid-sensing ion channels (ASICs), protons were usually considered as a modulator of other ion channels, such as voltage-gated calcium channels, N-methyl-d-aspartate, and gamma-amino butyric acid(A) receptor channels. Accordingly, the functional effects of acidosis were considered as consequences of modulations of these channels. Since the first cloning of ASICs in 1997, the conventional view on acidosis-mediated pain and cell injury has been dramatically changed. To date, ASICs, which are directly activated by extracellular protons, are shown to mediate most of the acidosis-associated physiological and pathological functions. For example, ASIC1a channels are reported to mediate acidosis-induced ischemic neuronal death. In this article, we will review the possible mechanisms that underlie ASIC1a channel-mediated neuronal death and discuss ASIC1a channel modulators involved in this process.
引用
收藏
页码:350 / 358
页数:9
相关论文
共 95 条
[1]   Modulation of ASIC channels in rat cerebellar Purkinje neurons by ischaemia-related signals [J].
Allen, NJ ;
Attwell, D .
JOURNAL OF PHYSIOLOGY-LONDON, 2002, 543 (02) :521-529
[2]   Amiloride is neuroprotective in an MPTP model of Parkinson's disease [J].
Arias, Robert L. ;
Sung, Mei-Li A. ;
Vasylyev, Dmytro ;
Zhang, Mei-Yi ;
Albinson, Kristin ;
Kubek, Katie ;
Kagan, Natasha ;
Beyer, Chad ;
Lin, Qian ;
Dwyer, Jason M. ;
Zaleska, Margaret M. ;
Bowlby, Mark R. ;
Dunlop, John ;
Monaghan, Michael .
NEUROBIOLOGY OF DISEASE, 2008, 31 (03) :334-341
[3]   Dramatic aggregation of Alzheimer Aβ by Cu(II) is induced by conditions representing physiological acidosis [J].
Atwood, CS ;
Moir, RD ;
Huang, XD ;
Scarpa, RC ;
Bacarra, NME ;
Romano, DM ;
Hartshorn, MK ;
Tanzi, RE ;
Bush, AI .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (21) :12817-12826
[4]   Protons act as a transmitter for muscle contraction in C-elegans [J].
Beg, Asim A. ;
Ernstrom, Glen G. ;
Nix, Paola ;
Davis, M. Wayne ;
Jorgensen, Erik M. .
CELL, 2008, 132 (01) :149-160
[5]   The neurotoxic MEC-4(d) DEG/ENaC sodium channel conducts calcium:: implications for necrosis initiation [J].
Bianchi, L ;
Gerstbrein, B ;
Frokjær-Jensen, C ;
Royal, DC ;
Mukherjee, G ;
Royal, MA ;
Xue, J ;
Schafer, WR ;
Driscoll, M .
NATURE NEUROSCIENCE, 2004, 7 (12) :1337-1344
[6]  
BOWEN BC, 1995, AM J NEURORADIOL, V16, P61
[7]   Effects of acidosis on the distribution and processing of the beta-amyloid precursor protein in cultured hippocampal neurons [J].
Brewer, GJ .
MOLECULAR AND CHEMICAL NEUROPATHOLOGY, 1997, 31 (02) :171-186
[8]   Activation of Acid-sensing Ion Channel 1a (ASIC1a) by Surface Trafficking [J].
Chai, Sunghee ;
Li, Minghua ;
Branigan, Deborah ;
Xiong, Zhi-Gang ;
Simon, Roger P. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2010, 285 (17) :13002-13011
[9]   ALKALINE EXTRACELLULAR PH SHIFTS GENERATED BY 2 TRANSMITTER-DEPENDENT MECHANISMS [J].
CHESLER, M ;
CHEN, JCT .
CANADIAN JOURNAL OF PHYSIOLOGY AND PHARMACOLOGY, 1992, 70 :S286-S292
[10]   Regulation and modulation of pH in the brain [J].
Chesler, M .
PHYSIOLOGICAL REVIEWS, 2003, 83 (04) :1183-1221