Role of connexin43 in central nervous system injury

被引:134
作者
Chew, Shenton S. L. [1 ]
Johnson, Cameron S. [1 ]
Green, Colin R. [1 ]
Danesh-Meyer, Helen V. [1 ]
机构
[1] Univ Auckland, Dept Ophthalmol, Fac Med & Hlth Sci, Auckland 1, New Zealand
关键词
Gap junctions; Ischemia; Trauma; Neuroprotection; ASTROCYTIC GAP-JUNCTIONS; RAT SPINAL-CORD; CELL-DEATH; INTERCELLULAR COMMUNICATION; KAINIC ACID; NEURONAL VULNERABILITY; NEUROPROTECTIVE ROLE; EFFECTIVE REDUCTION; OXIDATIVE STRESS; RODENT MODEL;
D O I
10.1016/j.expneurol.2010.07.014
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Gap junctions are specialized cell-to-cell contacts that provide direct intercellular communication. In the central nervous system (CNS), gap junction coupling occurs between both neurons and glial cells. One of the most abundant gap junction proteins in the CNS is connexin43 (Cx43). The functional syncytium formed by astrocytes via Cx43 gap junction intercellular communication has, for example, been implicated in maintaining the homeostasis of the extracellular milieu of neurons. In particular, astrocytes are involved in the spatial buffering of many ions, signalling molecules and energy sources. In this review, the role of Cx43 following CNS injury is examined by combining evidence surrounding the response of Cx43 to CNS injury and the effects of Cx43 gap junction blockade on neuronal survival in various models of injury. Combined evidence suggests that transient blockade targeting the window of initial Cx43 upregulation observed following injury is potentially therapeutic. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:250 / 261
页数:12
相关论文
共 89 条
[1]
Gap junction-mediated bystander effect in primary cultures of human malignant gliomas with recombinant expression of the HSVtk gene [J].
Asklund, T ;
Appelskog, IB ;
Ammerpohl, O ;
Langmoen, IA ;
Dilber, MS ;
Aints, A ;
Ekström, TJ ;
Almqvist, PM .
EXPERIMENTAL CELL RESEARCH, 2003, 284 (02) :185-195
[2]
New roles for astrocytes:: Gap junction hemichannels have something to communicate [J].
Bennett, MVL ;
Contreras, JE ;
Bukauskas, FF ;
Sáez, JC .
TRENDS IN NEUROSCIENCES, 2003, 26 (11) :610-617
[3]
Blanc EM, 1998, J NEUROCHEM, V70, P958
[4]
Endothelins regulate astrocyte gap junctions in rat hippocampal slices [J].
Blomstrand, F ;
Venance, L ;
Sirén, AL ;
Ezan, P ;
Hanse, E ;
Glowinski, J ;
Ehrenreich, H ;
Giaume, C .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2004, 19 (04) :1005-1015
[5]
Altered connexin expression after peripheral nerve injury [J].
Chandross, KJ ;
Kessler, JA ;
Cohen, RI ;
Simburger, E ;
Spray, DC ;
Bieri, P ;
Dermietzel, R .
MOLECULAR AND CELLULAR NEUROSCIENCE, 1996, 7 (06) :501-518
[6]
Nerve injury induces gap junctional coupling among axotomized adult motor neurons [J].
Chang, QA ;
Pereda, A ;
Pinter, MJ ;
Balice-Gordon, RJ .
JOURNAL OF NEUROSCIENCE, 2000, 20 (02) :674-684
[7]
INTERCELLULAR CALCIUM SIGNALING VIA GAP-JUNCTIONS IN GLIOMA-CELLS [J].
CHARLES, AC ;
NAUS, CCG ;
ZHU, DG ;
KIDDER, GM ;
DIRKSEN, ER ;
SANDERSON, MJ .
JOURNAL OF CELL BIOLOGY, 1992, 118 (01) :195-201
[8]
Role of connexin-based gap junction channels and hemichannels in ischemia-induced cell death in nervous tissue [J].
Contreras, JE ;
Sánchez, HA ;
Véliz, LP ;
Bukauskas, FF ;
Bennett, MVL ;
Sáez, JC .
BRAIN RESEARCH REVIEWS, 2004, 47 (1-3) :290-303
[9]
Metabolic inhibition induces opening of unapposed connexin 43 gap junction hemichannels and reduces gap junctional communication in cortical astrocytes in culture [J].
Contreras, JE ;
Sánchez, HA ;
Eugenin, EA ;
Speidel, D ;
Theis, M ;
Willecke, K ;
Bukauskas, FF ;
Bennett, MVL ;
Sáez, JC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (01) :495-500
[10]
Cotrina ML, 1998, J NEUROSCI, V18, P2520