The gap junction proteome and its relationship to disease

被引:217
作者
Laird, Dale W. [1 ]
机构
[1] Univ Western Ontario, Dept Anat & Cell Biol & Physiol & Pharmacol, London, ON N6A 5C1, Canada
基金
加拿大健康研究院;
关键词
DENTO-DIGITAL DYSPLASIA; DOWN-REGULATION; OCCLUDENS-1; AND-2; PLASMA-MEMBRANE; LIFE-CYCLE; CONNEXIN-43; CHANNELS; CX43; PHOSPHORYLATION; INTERNALIZATION;
D O I
10.1016/j.tcb.2009.11.001
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In recent years our understanding of connexins has advanced from viewing them simply as proteins with a surprisingly short lifespan that form gap junction channels. Connexins are now known to be multifaceted proteins at the core of many multiprotein complexes that link to structural junctional complexes and cytoskeletal elements, and also to the cellular machinery that facilitates their transport, assembly, function and internalization. Collectively, these connexin-binding proteins can be termed the 'gap junction proteome'. The mechanistic understanding of the gap junction proteome with regards to the dynamic life cycle of connexins has grown further in importance in light of the large number of human diseases attributed to connexin gene mutations and regulatory changes in connexin spatial localization and expression levels.
引用
收藏
页码:92 / 101
页数:10
相关论文
共 92 条
[1]   Connexin 43 downregulation and dephosphorylation in nonischemic heart failure is associated with enhanced colocalized protein phosphatase type 2A [J].
Ai, X ;
Pogwizd, SM .
CIRCULATION RESEARCH, 2005, 96 (01) :54-63
[2]   Molecular cloning and functional analysis of a novel Cx43 partner protein CIP150 [J].
Akiyama, M ;
Ishida, N ;
Ogawa, T ;
Yogo, K ;
Takeya, T .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2005, 335 (04) :1264-1271
[3]   The TSG101 protein binds to connexins and is involved in connexin degradation [J].
Auth, Tanja ;
Schlueter, Sharazad ;
Urschel, Stephanie ;
Kussmann, Petra ;
Sonntag, Stephan ;
Hoeher, Thorsten ;
Kreuzberg, Maria M. ;
Dobrowolski, Radoslaw ;
Willecke, Klaus .
EXPERIMENTAL CELL RESEARCH, 2009, 315 (06) :1053-1062
[4]   Hemichannels in Cerebral Ischemia [J].
Bargiotas, Panagiotis ;
Monyer, Hannah ;
Schwaninger, Markus .
CURRENT MOLECULAR MEDICINE, 2009, 9 (02) :186-194
[5]   Dephosphorylation and intracellular redistribution of ventricular connexin43 during electrical uncoupling induced by ischemia [J].
Beardslee, MA ;
Lerner, DL ;
Tadros, PN ;
Laing, JG ;
Beyer, EC ;
Yamada, KA ;
Kléber, AG ;
Schuessler, RB ;
Saffitz, JE .
CIRCULATION RESEARCH, 2000, 87 (08) :656-662
[6]   GJA12 mutations in children with recessive hypomyelinating leukoencephalopathy [J].
Bugiani, M. ;
Al Shahwan, S. ;
Lamantea, E. ;
Bizzi, A. ;
Bakhsh, E. ;
Moroni, I. ;
Balestrini, M. R. ;
Uziel, G. ;
Zeviani, M. .
NEUROLOGY, 2006, 67 (02) :273-279
[7]   Drebrin is a novel connexin-43 binding partner that links gap junctions to the submembrane cytoskeleton [J].
Butkevich, E ;
Hülsmann, S ;
Wenzel, D ;
Shirao, T ;
Duden, R ;
Majoul, I .
CURRENT BIOLOGY, 2004, 14 (08) :650-658
[8]   Gap Junctions and Cancer: New Functions for an Old Story [J].
Cronier, Laurent ;
Crespin, Sophie ;
Strale, Pierre-Olivier ;
Defamie, Norah ;
Mesnil, Marc .
ANTIOXIDANTS & REDOX SIGNALING, 2009, 11 (02) :323-338
[9]  
DAS S, 2008, CELL COMMUN ADHES, V15, P65
[10]   ERp29 Restricts Connexin43 Oligomerization in the Endoplasmic Reticulum [J].
Das, Shamie ;
Smith, Tekla D. ;
Das Sarma, Jayasri ;
Ritzenthaler, Jeffrey D. ;
Maza, Jose ;
Kaplan, Benjamin E. ;
Cunningham, Leslie A. ;
Suaud, Laurence ;
Hubbard, Michael J. ;
Rubenstein, Ronald C. ;
Koval, Michael .
MOLECULAR BIOLOGY OF THE CELL, 2009, 20 (10) :2593-2604