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Review
. 2009 Aug;19(6):182-90.
doi: 10.1016/j.tcm.2009.12.001.

Cell-cell connection to cardiac disease

Affiliations
Review

Cell-cell connection to cardiac disease

Farah Sheikh et al. Trends Cardiovasc Med. 2009 Aug.

Abstract

Intercalated disks (ICDs) are highly organized cell-cell adhesion structures, which connect cardiomyocytes to one another. They are composed of three major complexes: desmosomes, fascia adherens, and gap junctions. Desmosomes and fascia adherens junction are necessary for mechanically coupling and reinforcing cardiomyocytes, whereas gap junctions are essential for rapid electrical transmission between cells. Because human genetics and mouse models have revealed that mutations and/or deficiencies in various ICD components can lead to cardiomyopathies and arrhythmias, considerable attention has focused on the biologic function of the ICD. This review will discuss recent scientific developments related to the ICD and focus on its role in regulating cardiac muscle structure, signaling, and disease.

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Figures

Figure 1
Figure 1
Transmission electron micrograph of the major junctional components within the ICD of an adult mouse heart. Fa indicates fascia adherens junction; Ds, desmosome; and Gj, gap junction. White bar represents 500 nm.
Figure 2
Figure 2
Schemata of the major complexes and components found in the cardiac ICD.

References

    1. Alcalai R, et al. A recessive mutation in desmoplakin causes arrhythmogenic right ventricular dysplasia, skin disorder, and woolly hair. J Am Coll Cardiol. 2003;42:319–327. - PubMed
    1. Antoniades L, et al. Arrhythmogenic right ventricular cardiomyopathy caused by deletions in plakophilin-2 and plakoglobin (Naxos disease) in families from Greece and Cyprus: genotype-phenotype relations, diagnostic features and prognosis. Eur Heart J. 2006;27:2208–2216. - PubMed
    1. Asimaki A, et al. A novel dominant mutation in plakoglobin causes arrhythmogenic right ventricular cardiomyopathy. Am J Hum Genet. 2007;81:964–973. - PMC - PubMed
    1. Bauce B, et al. Clinical profile of four families with arrhythmogenic right ventricular cardiomyopathy caused by dominant desmoplakin mutations. Eur Heart J. 2005;26:1666–1675. - PubMed
    1. Beffagna G, et al. Missense mutations in desmocollin-2 N-terminus, associated with arrhythmogenic right ventricular cardiomyopathy, affect intracellular localization of desmocollin-2 in vitro. BMC Med Genet. 2007;8:65. - PMC - PubMed

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