Editorials |
From the Department of Pharmacology, College of Physicians and Surgeons, Columbia University, New York, NY.
Correspondence to Heather S. Duffy, Department of Pharmacology, College of Physicians and Surgeons, Columbia University, 630 W 168th St, New York, NY 10032. E-mail hsd2102@columbia.edu
See related article, pages 646655
Key Words: arrhythmogenic right ventricular dysplasia/cardiomyopathy carvajal syndrome desmosomes cell adhesion
An extract of the first 250 words of the full text is provided, because this article has no abstract. |
Two cardiomyopathies ascribed to desmosomal mutations have been described: Naxos disease which gives rise to arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C),1 and Carvajal syndrome,2 in which the cardiac pathology is primarily left-sided. How do mutations in a single junctional type lead to such disparate results? In this edition of Circulation Research, Yang et al3 describe a novel desmosomal protein mutation that may shed some light on this perplexing question.
Desmosomes were originally given the name "mechanical" or "attachment junctions" describing what was thought to be their main role, cell stabilization. They were called the "glue" that held the tissue together. It has long been assumed that the loss of the "glue" causes disease by providing weak cellcell interactions in tissues that require strong connections. Desmosomes are comprised of multiple proteins which interact to form a macromolecular complex4 that links the intermediate filaments (desmin in cardiac myocytes) of one cell to the intermediate filaments of the adjacent cells through the transmembrane proteins (Figure, A). The transmembrane domain portion is formed from 2 distinct cadherin proteins, desmocollin and desmoglein which bind to the intracellular linker protein, plakoglobin. Then, via its amino-terminal domain, desmoplakin binds to plakoglobin. The link to the cytoskeleton occurs with the binding of the intermediate filaments with the carboxyl-terminal domain of desmoplakin, an event required for tissue stability. Another cohort protein, plakophilin, also binds plakoglobin and is thought to be important in desmosomal stability. Some component proteins of the desmosome have been shown to be involved in
Related Article:
Circ. Res. 2006 99: 646-655.
|
Circulation Research Home | Subscriptions | Archives | Feedback | Authors | Help | AHA Journals Home | Search Copyright © 2006 American Heart Association, Inc. All rights reserved. Unauthorized use prohibited. |