Managing the complexity of communication: regulation of gap junctions by post-translational modification

被引:99
作者
Axelsen, Lene N. [1 ,2 ]
Calloe, Kirstine [3 ]
Holstein-Rathlou, Niels-Henrik [1 ,2 ]
Nielsen, Morten S. [1 ,2 ]
机构
[1] Univ Copenhagen, Fac Med & Hlth Sci, Dept Biomed Sci, DK-2200 Copenhagen, Denmark
[2] Univ Copenhagen, Fac Med & Hlth Sci, Danish Natl Res Fdn Ctr Cardiac Arrhythmia, DK-2200 Copenhagen, Denmark
[3] Univ Copenhagen, Fac Med & Hlth Sci, Dept Vet Clin & Anim Sci, DK-2200 Copenhagen, Denmark
基金
新加坡国家研究基金会;
关键词
connexin; post translational modification; phosphorylation; sumoylation; nitrosylation; methylation; acetylation; ubiquitination; PROTEIN-KINASE-C; PROTEASOME-DEPENDENT DEGRADATION; MICROVASCULAR ENDOTHELIAL-CELLS; V-SRC; INTRACELLULAR-TRANSPORT; PHOSPHORYLATION SITES; S-NITROSYLATION; DOWN-REGULATION; IN-VIVO; CONNEXIN-43; PHOSPHORYLATION;
D O I
10.3389/fphar.2013.00130
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Gap junctions are comprised of connexins that form cell-to-cell channels which couple neighboring cells to accommodate the exchange of information. The need for communication does, however, change over time and therefore must be tightly controlled. Although the regulation of connexin protein expression by transcription and translation is of great importance, the trafficking, channel activity and degradation are also under tight control. The function of connexins can be regulated by several post translational modifications, which affect numerous parameters; including number of channels, open probability, single channel conductance or selectivity. The most extensively investigated post translational modifications are phosphorylations, which have been documented in all mammalian connexins. Besides phosphorylations, some connexins are known to be ubiquitinated, SUMOylated, nitrosylated, hydroxylated, acetylated, methylated, and y-carboxyglutamated. The aim of the present review is to summarize our current knowledge of post translational regulation of the connexin family of proteins.
引用
收藏
页数:18
相关论文
共 161 条
[41]   Phosphorylated carboxy terminal serine residues stabilize the mouse gap junction protein connexin45 against degradation [J].
Hertlein, B ;
Butterweck, A ;
Haubrich, S ;
Willecke, K ;
Traub, O .
JOURNAL OF MEMBRANE BIOLOGY, 1998, 162 (03) :247-257
[42]   Regulation by S-Nitrosylation of Protein Post-translational Modification [J].
Hess, Douglas T. ;
Stamler, Jonathan S. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2012, 287 (07) :4411-4418
[43]   Protein S-nitrosylation:: Purview and parameters [J].
Hess, DT ;
Matsumoto, A ;
Kim, SO ;
Marshall, HE ;
Stamler, JS .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2005, 6 (02) :150-166
[44]   Phosphatidylinositol-bisphosphate regulates intercellular coupling in cardiac myocytes [J].
Hofgaard, Johannes P. ;
Banach, Kathrin ;
Mollerup, Sarah ;
Jorgensen, Helene Korvenius ;
Olesen, Soren Peter ;
Holstein-Rathlou, Niels-Henrik ;
Nielsen, Morten Schak .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 2008, 457 (02) :303-313
[45]   Effects of streptozotocin-induced diabetes on connexin43 mRNA and protein expression in ventricular muscle [J].
Howarth, F. C. ;
Chandler, N. J. ;
Kharche, S. ;
Tellez, J. O. ;
Greener, I. D. ;
Yamanushi, T. T. ;
Billeter, R. ;
Boyett, M. R. ;
Zhang, H. ;
Dobrzynski, H. .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 2008, 319 (1-2) :105-114
[46]   Identification of CaMKII Phosphorylation Sites in Connexin43 by High-Resolution Mass Spectrometry [J].
Huang, Richard Y-C. ;
Laing, James G. ;
Kanter, Evelyn M. ;
Berthoud, Viviana M. ;
Bao, Mingwei ;
Rohrs, Henry W. ;
Townsend, R. Reid ;
Yamada, Kathryn A. .
JOURNAL OF PROTEOME RESEARCH, 2011, 10 (03) :1098-1109
[47]   A FAMILY OF PROTEINS STRUCTURALLY AND FUNCTIONALLY RELATED TO THE E6-AP UBIQUITIN-PROTEIN LIGASE (VOL 92, PG 2563, 1995) [J].
HUIBREGTSE, JM ;
SCHEFFNER, M ;
BEAUDENON, S ;
HOWLEY, PM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (11) :5249-5249
[48]  
Ikeda F, 2008, EMBO REP, V9, P536, DOI 10.1038/embor.2008.93
[49]   PI3K/Akt signaling is involved in the disruption of gap junctional communication caused by v-Src and TNF-α [J].
Ito, Satoko ;
Hyodo, Toshinori ;
Hasegawa, Hitoki ;
Yuan, Hong ;
Hamaguchi, Michinari ;
Senga, Takeshi .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2010, 400 (02) :230-235
[50]   Ischemia-induced dephosphorylation of cardiomyocyte connexin-43 is reduced by okadaic acid and calyculin A but not fostriecin [J].
Jeyaraman, M ;
Tanguy, S ;
Fandrich, RR ;
Lukas, A ;
Kardami, E .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 2003, 242 (1-2) :129-134