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Updated: Mar 31, 2026

Perturbing Endothelial Biomechanics via Connexin 43 Structural Disruption
Published on: October 4, 2019
Role of connexin 43 in cardiovascular diseases
Pecoraro Michela1, Verrilli Velia1, Pinto Aldo1
1Department of Pharmacy, University of Salerno, Italy.
Insights
Cardiac gap junctions, particularly Connexin 43 (Cx43), are vital for heart function. Remodeling of these junctions is linked to various cardiac diseases, including heart failure and ischemia.
Area of Science:
- Cardiovascular Biology
- Cellular Communication
- Mitochondrial Function
Background:
- Gap junctions (GJs) facilitate intercellular communication essential for cardiac rhythm, vascular tone, and endothelial function.
- Connexin 43 (Cx43) is the predominant GJ isoform in cardiomyocytes, enabling cell-to-cell transfer of molecules and signals.
- Cx43 is also found in mitochondria, playing a role in ischemic preconditioning.
Purpose of the Study:
- To review the current understanding of cardiac gap junction remodeling in the context of cardiovascular diseases.
- To explore the role of Connexin 43 (Cx43) in both intercellular communication and mitochondrial function within the heart.
Main Methods:
- Literature review of studies on cardiac gap junctions and cardiovascular pathology.
- Analysis of research on Connexin 43 (Cx43) expression, distribution, and function.
- Synthesis of findings related to GJ remodeling in conditions like hypertrophy, heart failure, and ischemia.
Main Results:
- Alterations in Cx43 expression and localization are hallmarks of myocardial diseases.
- Mitochondrial Cx43 is implicated in cardioprotective mechanisms such as ischemic preconditioning.
- Remodeling of cardiac gap junctions significantly impacts cardiac health and disease progression.
Conclusions:
- Cardiac gap junctions, especially Cx43, are critical for maintaining cardiovascular homeostasis.
- Dysfunctional gap junctions and Cx43 alterations are strongly associated with the pathogenesis of heart diseases.
- Targeting gap junction remodeling may offer therapeutic strategies for cardiovascular conditions.
Abstract:
Gap junctions (GJs) channels provide the basis for intercellular communication in the cardiovascular system for maintenance of the normal cardiac rhythm, regulation of vascular tone and endothelial function as well as metabolic interchange between the cells. They allow the transfer of small molecules and may enable slow calcium wave spreading, transfer of "death" or of "survival" signals. In the cardiomyocytes the most abundant isoform is Connexin 43 (Cx43). Alterations in Cx43 expression and distribution were observed in myocardium disease; i.e. in hypertrophic cardiomyopathy, heart failure and ischemia. Recent reports suggest the presence of Cx43 in the mitochondria as well, at least in the inner mitochondrial membrane, where it plays a central role in ischemic preconditioning. In this review, the current knowledge on the relationship between the remodeling of cardiac gap junctions and cardiac diseases are summarized.
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