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Updated: Feb 5, 2026

Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
Connexin 43: a New Therapeutic Target Against Chronic Kidney Disease
Niki Prakoura1, Panagiotis Kavvadas1, Christos E Chadjichristos1,2
1Institut National de la Santé Et de la Recherche Médicale UMRS 1155, Tenon Hospital, Paris, France.
Abstract:
Chronic kidney disease is an incurable to date pathology with a continuously growing incidence that contributes to the increase of the number of deaths worldwide. With currently no efficient prognostic or therapeutic options being available, the only possibility for treatment of end-stage renal disease is renal replacement therapy through dialysis or transplantation. Understanding the molecular mechanisms participating in the progression of renal diseases and uncovering the pathways implicated will permit the identification of novel and more efficient targets of therapy. Connexin43 was recently identified as a novel player in the development of chronic kidney disease. It was found de novo expressed and/or differentially localized in various renal cell populations during progression of renal disease, indicating an abnormal connexin signaling, both in patients and animal models. Subsequent in vivo studies demonstrated that connexin43 is involved in mediating inflammatory and fibrotic processes contributing to renal damage. Genetic, pharmaco-genetic or peptide-based inhibition of connexin43 in animal models and cell culture systems was successful in preventing the progression of the pathology and preserving the cell phenotypes. This review will summarize the recent advances on connexin43 in the field of kidney diseases and discuss the potential of future connexin43-based therapies against chronic kidney disease.
Insights
Chronic kidney disease (CKD) involves abnormal connexin43 signaling, contributing to inflammation and fibrosis. Inhibiting connexin43 in studies prevented CKD progression, suggesting it as a therapeutic target.
Area of Science:
- Nephrology
- Molecular Biology
- Pathology
Background:
- Chronic kidney disease (CKD) is a growing global health issue with limited treatment options.
- Current treatments for end-stage renal disease (ESRD) include dialysis and transplantation.
- Understanding CKD's molecular mechanisms is crucial for developing new therapies.
Purpose of the Study:
- To review recent advances in understanding connexin43's role in kidney disease.
- To discuss the potential of connexin43-based therapies for CKD.
Main Methods:
- Review of existing literature on connexin43 in kidney disease.
- Analysis of studies involving connexin43 expression and localization in renal cells.
- Examination of in vivo and cell culture studies on connexin43 inhibition.
Main Results:
- Connexin43 is aberrantly expressed and localized in renal cells during CKD progression.
- Connexin43 mediates inflammatory and fibrotic processes in the kidney.
- Inhibition of connexin43 in preclinical models prevented CKD progression and preserved renal cell phenotypes.
Conclusions:
- Connexin43 is a significant factor in CKD development and progression.
- Targeting connexin43 offers a promising therapeutic strategy for managing chronic kidney disease.
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