Intercalated discs: cellular adhesion and signaling in heart health and diseases

• Published in: Heart failure reviews 2019, Vol.24 (1), p.115-132
• Main Authors: Zhao, Guangze, Qiu, Ye, Zhang, Huifang M., Yang, Decheng
• Format: Article
• Language: English
• Subjects: Actin; Adherens Junctions - chemistry; Adherens Junctions - genetics; Adherens Junctions - metabolism; Animals; Calcineurin; Cardiology; Cardiomyocytes; Cardiomyopathy; Cell Adhesion; Cell adhesion & migration; Cell membranes; Coronary artery disease; Cytoplasm; Cytoskeleton; Desmosomes; Desmosomes - chemistry; Desmosomes - genetics; Desmosomes - metabolism; Dilated cardiomyopathy; Gap junctions; Gap Junctions - chemistry; Gap Junctions - genetics; Gap Junctions - metabolism; Heart diseases; Heart Diseases - genetics; Heart Diseases - metabolism; Heart failure; Humans; Kinases; MAP kinase; Medicine; Medicine & Public Health; Mutation; Mutation, Missense; Myocardium; Myocardium - metabolism; Myocytes, Cardiac - metabolism; NF-AT protein; Serum response factor; Signal Transduction; Ventricle; Wnt protein; β-Catenin
• ISSN: 1382-4147; 1573-7322
• DOI: 10.1007/s10741-018-9743-7

Intercalated discs (ICDs) are highly orchestrated structures that connect neighboring cardiomyocytes in the heart. Three major complexes are distinguished in ICD: desmosome, adherens junction (AJ), and gap junction (GJ). Desmosomes are major cell adhesion junctions that anchor cell membrane to the intermediate filament network; AJs connect the actin cytoskeleton of adjacent cells; and gap junctions metabolically and electrically connect the cytoplasm of adjacent cardiomyocytes. All these complexes work as a single unit, the so-called area composita, interdependently rather than individually. Mutation or altered expression of ICD proteins results in various cardiac diseases, such as ARVC (arrhythmogenic right ventricular cardiomyopathy), dilated cardiomyopathy, and hypotrophy cardiomyopathy, eventually leading to heart failure. In this article, we first review the recent findings on the structural organization of ICD and their functions and then focus on the recent advances in molecular pathogenesis of the ICD-related heart diseases, which include two major areas: i) the ICD gene mutations in cardiac diseases, and ii) the involvement of ICD proteins in signal transduction pathways leading to myocardium remodeling and eventual heart failure. These major ICD-related signaling pathways include Wnt/β-catenin pathway, p38 MAPK cascade, Rho-dependent serum response factor (SRF) signaling, calcineurin/NFAT signaling, Hippo kinase cascade, etc., which are differentially regulated in pathological conditions.