cAMP: A master regulator of cadherin‐mediated binding in endothelium, epithelium and myocardium

• Published in: Acta Physiologica 2023-08, Vol.238 (4), p.e14006-n/a
• Main Authors: Vielmuth, Franziska, Radeva, Mariya Y., Yeruva, Sunil, Sigmund, Anna M., Waschke, Jens
• Format: Article
• Language: English
• Subjects: adherens junction; Adherens junctions; cadherin; Cadherins; Cadherins - metabolism; Cadherins - pharmacology; cAMP; Cardiomyocytes; Cardiomyopathy; Catenin; Cell adhesion; Cell adhesion & migration; Cell Adhesion - physiology; Cyclic AMP; desmosome; Desmosomes - metabolism; Endothelium; Endothelium - metabolism; Epithelial cells; Epithelium; Epithelium - metabolism; Humans; Keratinocytes; Kinases; Molecular modelling; Myocardium; Myocardium - metabolism; Pemphigus; Pemphigus - metabolism; Pemphigus - pathology; Phosphodiesterase IV; Phosphorylation; Protein kinase A; Proteins; Therapeutic targets
• ISSN: 1748-1708; 1748-1716
• DOI: 10.1111/apha.14006

Regulation of cadherin‐mediated cell adhesion is crucial not only for maintaining tissue integrity and barrier function in the endothelium and epithelium but also for electromechanical coupling within the myocardium. Therefore, loss of cadherin‐mediated adhesion causes various disorders, including vascular inflammation and desmosome‐related diseases such as the autoimmune blistering skin dermatosis pemphigus and arrhythmogenic cardiomyopathy. Mechanisms regulating cadherin‐mediated binding contribute to the pathogenesis of diseases and may also be used as therapeutic targets. Over the last 30 years, cyclic adenosine 3′,5′‐monophosphate (cAMP) has emerged as one of the master regulators of cell adhesion in endothelium and, more recently, also in epithelial cells as well as in cardiomyocytes. A broad spectrum of experimental models from vascular physiology and cell biology applied by different generations of researchers provided evidence that not only cadherins of endothelial adherens junctions (AJ) but also desmosomal contacts in keratinocytes and the cardiomyocyte intercalated discs are central targets in this scenario. The molecular mechanisms involve protein kinase A‐ and exchange protein directly activated by cAMP‐mediated regulation of Rho family GTPases and S665 phosphorylation of the AJ and desmosome adaptor protein plakoglobin. In line with this, phosphodiesterase 4 inhibitors such as apremilast have been proposed as a therapeutic strategy to stabilize cadherin‐mediated adhesion in pemphigus and may also be effective to treat other disorders where cadherin‐mediated binding is compromised.