A novel mechanism of depression: role for connexins

被引:38
作者
Xia, Cong-Yuan [1 ,2 ,3 ]
Wang, Zhen-Zhen [1 ,2 ,3 ]
Yamakuni, Tohru [5 ]
Chen, Nai-Hong [1 ,2 ,3 ,4 ]
机构
[1] Chinese Acad Med Sci, Inst Mat Med, State Key Lab Bioact Subst & Funct Nat Med, Beijing 100050, Peoples R China
[2] Chinese Acad Med Sci, Neurosci Ctr, Beijing 100050, Peoples R China
[3] Peking Union Med Coll, Beijing 100050, Peoples R China
[4] Hunan Univ Chinese Med, Coll Pharm, Changsha 410208, Hunan, Peoples R China
[5] Tohoku Univ, Grad Sch Pharmaceut Sci, Sendai, Miyagi 9808578, Japan
基金
中国国家自然科学基金; 中国博士后科学基金; 北京市自然科学基金;
关键词
Depression; Connexins; Gap junction; Hemichannels; GAP-JUNCTION CHANNELS; INTERCELLULAR CALCIUM WAVE; DEPENDENT PROTEIN-KINASE; MOUSE PREFRONTAL CORTEX; ISCHEMIC BRAIN-INJURY; NECROSIS-FACTOR-ALPHA; MITOCHONDRIAL CONNEXIN-43; GLIAL-CELLS; ELECTRICAL SYNAPSES; ACTIVATED MICROGLIA;
D O I
10.1016/j.euroneuro.2018.01.009
中图分类号
R74 [神经病学与精神病学];
学科分类号
100204 [神经病学];
摘要
Major depressive disorder (MDD) is a chronic and debilitating illness that affects over 350 million people worldwide; however, current treatments have failed to cure or prevent the progress of depression. Increasing evidence suggests a crucial role for connexins in MDD. In this review, we have summarised recent accomplishments regarding the role of connexins, gap junctions, and hemichannels in the aetiology of MDD, and discussed the limitations of current research. A blockage of gap junctions or hemichannels induces depressive behaviour. Possible underlying mechanisms include the regulation of neurosecretory functions and synaptic activity by gap junctions and hemichannels. Gap junctions are functionally inhibited under stress conditions. Conversely, hemichannel permeability is increased. Antidepressants inhibit hemichannel permeability; however, they have contrasting effects on the function of gap junctions under normal conditions and can protect them against stress. In conclusion, the blockage of hemichannels concurrent with improvements in gap junction functionality might be potential targets for depression treatment. (C) 2018 Elsevier B.V. and ECNP. All rights reserved.
引用
收藏
页码:483 / 498
页数:16
相关论文
共 174 条
[51]
Injury-triggered Akt phosphorylation of Cx43: a ZO-1-driven molecular switch that regulates gap junction size [J].
Dunn, Clarence A. ;
Lampe, Paul D. .
JOURNAL OF CELL SCIENCE, 2014, 127 (02) :455-464
[52]
Dysfunction of Astrocyte Connexins 30 and 43 in Dorsal Lateral Prefrontal Cortex of Suicide Completers [J].
Ernst, Carl ;
Nagy, Corina ;
Kim, Sangyheon ;
Yang, Jennie P. ;
Deng, Xiaoming ;
Hellstrom, Ian C. ;
Choi, Kwang Ho ;
Gershenfeld, Howard ;
Meaney, Michael J. ;
Turecki, Gustavo .
BIOLOGICAL PSYCHIATRY, 2011, 70 (04) :312-319
[53]
Microglia at brain stab wounds express connexin 43 and in vitro form functional gap junctions after treatment with interferon-γ and tumor necrosis factor-α [J].
Eugenín, EA ;
Eckardt, D ;
Theis, M ;
Willecke, K ;
Bennett, MVL ;
Sáez, JC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (07) :4190-4195
[54]
ATP-sensitive potassium channels: uncovering novel targets for treating depression [J].
Fan, Yi ;
Kong, Hui ;
Ye, Xinhai ;
Ding, Jianhua ;
Hu, Gang .
BRAIN STRUCTURE & FUNCTION, 2016, 221 (06) :3111-3122
[55]
Chronic psychotropic drug treatment causes differential expression of connexin 43 and GFAP in frontal cortex of rats [J].
Fatemi, S. Hossein ;
Folsom, Timothy D. ;
Reutiman, Teri J. ;
Pandian, Twinkle ;
Braun, Natalie N. ;
Haug, Kari .
SCHIZOPHRENIA RESEARCH, 2008, 104 (1-3) :127-134
[56]
Psychiatric comorbidity in 36 adults with mitochondrial cytopathies [J].
Fattal, Omar ;
Link, Jessica ;
Quinn, Kathleen ;
Cohen, Bruce H. ;
Franco, Kathleen .
CNS SPECTRUMS, 2007, 12 (06) :429-438
[57]
Gap junctional control of glial glutamate transporter expression [J].
Figiel, Maciej ;
Allritz, Claudia ;
Lehmann, Claudia ;
Engele, Juergen .
MOLECULAR AND CELLULAR NEUROSCIENCE, 2007, 35 (01) :130-137
[58]
EGF induces efficient Cx43 gap junction endocytosis in mouse embryonic stem cell colonies via phosphorylation of Ser262, Ser279/282, and Ser368 [J].
Fong, John T. ;
Nimlamool, Wutigri ;
Falk, Matthias M. .
FEBS LETTERS, 2014, 588 (05) :836-844
[59]
The Liver Connexin32 Interactome Is a Novel Plasma Membrane-Mitochondrial Signaling Nexus [J].
Fowler, Stephanie L. ;
Akins, Mark ;
Zhou, Hu ;
Figeys, Daniel ;
Bennett, Steffany A. L. .
JOURNAL OF PROTEOME RESEARCH, 2013, 12 (06) :2597-2610
[60]
Gadicherla A. K., 2017, MITOCHONDRIAL C 43 H, V112, P27