Literature DB >> 26073311

Connexin 43 is an emerging therapeutic target in ischemia/reperfusion injury, cardioprotection and neuroprotection.

Rainer Schulz1, Philipp Maximilian Görge2, Anikó Görbe3, Péter Ferdinandy4, Paul D Lampe5, Luc Leybaert6.   

Abstract

Connexins are widely distributed proteins in the body that are crucially important for heart and brain functions. Six connexin subunits form a connexon or hemichannel in the plasma membrane. Interactions between two hemichannels in a head-to-head arrangement result in the formation of a gap junction channel. Gap junctions are necessary to coordinate cell function by passing electrical current flow between heart and nerve cells or by allowing exchange of chemical signals and energy substrates. Apart from its localization at the sarcolemma of cardiomyocytes and brain cells, connexins are also found in the mitochondria where they are involved in the regulation of mitochondrial matrix ion fluxes and respiration. Connexin expression is affected by age and gender as well as several pathophysiological alterations such as hypertension, hypertrophy, diabetes, hypercholesterolemia, ischemia, post-myocardial infarction remodeling or heart failure, and post-translationally connexins are modified by phosphorylation/de-phosphorylation and nitros(yl)ation which can modulate channel activity. Using knockout/knockin technology as well as pharmacological approaches, one of the connexins, namely connexin 43, has been identified to be important for cardiac and brain ischemia/reperfusion injuries as well as protection from it. Therefore, the current review will focus on the importance of connexin 43 for irreversible injury of heart and brain tissues following ischemia/reperfusion and will highlight the importance of connexin 43 as an emerging therapeutic target in cardio- and neuroprotection.
Copyright © 2015 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Brain; Cardioprotection; Connexin 43; Heart; Mitochondria; Neuroprotection

Mesh:

Substances:

Year:  2015        PMID: 26073311      PMCID: PMC4599355          DOI: 10.1016/j.pharmthera.2015.06.005

Source DB:  PubMed          Journal:  Pharmacol Ther        ISSN: 0163-7258            Impact factor:   12.310


  337 in total

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5.  Cyclic mechanical stretch induces cardiomyocyte orientation and polarization of the gap junction protein connexin43.

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6.  Inhibiting N-cadherin-mediated adhesion affects gap junction communication in isolated rat hearts.

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Journal:  Cell Death Differ       Date:  2008-09-26       Impact factor: 15.828

8.  Ischemic preconditioning preserves connexin 43 phosphorylation during sustained ischemia in pig hearts in vivo.

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Journal:  Exp Clin Cardiol       Date:  2004

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  84 in total

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Review 3.  Current Modalities and Mechanisms Underlying Cardioprotection by Ischemic Conditioning.

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Review 5.  The role of glycine in regulated cell death.

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6.  The gap junction modifier ZP1609 decreases cardiomyocyte hypercontracture following ischaemia/reperfusion independent from mitochondrial connexin 43.

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Review 7.  Regulation of cardiac gap junctions by protein phosphatases.

Authors:  Ashleigh R Hood; Xun Ai; Steven M Pogwizd
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Review 8.  Tumor-targeted nanotherapeutics: overcoming treatment barriers for glioblastoma.

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9.  The SH3-binding domain of Cx43 participates in loop/tail interactions critical for Cx43-hemichannel activity.

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10.  Modulating cardiac conduction during metabolic ischemia with perfusate sodium and calcium in guinea pig hearts.

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