Cell-cell connectivity: desmosomes and disease

被引:141
作者
Brooke, Matthew A. [1 ]
Nitoiu, Daniela [1 ]
Kelsell, David P. [1 ]
机构
[1] Queen Mary Univ London, Barts & London Sch Med & Dent, Blizard Inst, Ctr Cutaneous Res, London E1 2AT, England
关键词
desmosome; cadherins; desmoplakin; hyperadhesion; proteases; pemphigus; cystatin A; ADAM17; ARVC; PEMPHIGUS-VULGARIS-IGG; RIGHT-VENTRICULAR CARDIOMYOPATHY; TIGHT-JUNCTION PROTEIN; HEART-MUSCLE CELLS; ECTODERMAL DYSPLASIA; BULLOUS IMPETIGO; SKIN-DISEASE; BETA-CATENIN; PALMOPLANTAR KERATODERMA; COMPOUND HETEROZYGOSITY;
D O I
10.1002/path.3027
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Cell-cell connectivity is an absolute requirement for the correct functioning of cells, tissues and entire organisms. At the level of the individual cell, direct cell-cell adherence and communication is mediated by the intercellular junction complexes: desmosomes, adherens, tight and gap junctions. A broad spectrum of inherited, infectious and auto-immune diseases can affect the proper function of intercellular junctions and result in either diseases affecting specific individual tissues or widespread syndromic conditions. A particularly diverse group of diseases result from direct or indirect disruption of desmosomes-a consequence of their importance in tissue integrity, their extensive distribution, complex structure, and the wide variety of functions their components accomplish. As a consequence, disruption of desmosomal assembly, structure or integrity disrupts not only their intercellular adhesive function but also their functions in cell communication and regulation, leading to such diverse pathologies as cardiomyopathy, epidermal and mucosal blistering, palmoplantar keratoderma, woolly hair, keratosis, epidermolysis bullosa, ectodermal dysplasia and alopecia. Here, as well as describing the importance of the other intercellular junctions, we focus primarily on the desmosome, its structure and its role in disease. We will examine the various pathologies that result from impairment of desmosome function and thereby demonstrate the importance of desmosomes to tissues and to the organism as a whole. Copyright (C) 2011 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.
引用
收藏
页码:158 / 171
页数:14
相关论文
共 185 条
[1]
Plakoglobin Is Required for Effective Intermediate Filament Anchorage to Desmosomes [J].
Acehan, Devrim ;
Petzold, Christopher ;
Gumper, Iwona ;
Sabatini, David D. ;
Mueller, Eliane J. ;
Cowin, Pamela ;
Stokes, David L. .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2008, 128 (11) :2665-2675
[2]
CONFORMATIONAL EPITOPES OF PEMPHIGUS ANTIGENS (DSG1 AND DSG3) ARE CALCIUM-DEPENDENT AND GLYCOSYLATION INDEPENDENT [J].
AMAGAI, M ;
ISHII, K ;
HASHIMOTO, T ;
GAMOU, S ;
SHIMIZU, N ;
NISHIKAWA, T .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1995, 105 (02) :243-247
[3]
Toxin in bullous impetigo and staphylococcal scalded-skin syndrome targets desmoglein 1 [J].
Amagai, M ;
Matsuyoshi, N ;
Wang, ZH ;
Andl, C ;
Stanley, JR .
NATURE MEDICINE, 2000, 6 (11) :1275-1277
[4]
AUTOANTIBODIES AGAINST A NOVEL EPITHELIAL CADHERIN IN PEMPHIGUS-VULGARIS, A DISEASE OF CELL-ADHESION [J].
AMAGAI, M ;
KLAUSKOVTUN, V ;
STANLEY, JR .
CELL, 1991, 67 (05) :869-877
[5]
Staphylococcal exfoliative toxin B specifically cleaves desmoglein 1 [J].
Amagai, M ;
Yamaguchi, T ;
Hanakawa, Y ;
Nishifuji, K ;
Sugai, M ;
Stanley, JR .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2002, 118 (05) :845-850
[6]
Physiology and Function of the Tight Junction [J].
Anderson, James M. ;
Van Itallie, Christina M. .
COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY, 2009, 1 (02) :a002584
[7]
ANGST BD, 1990, J CELL SCI, V97, P247
[8]
Binding of pemphigus vulgaris IgG to antigens in desmosome core domains excludes immune complexes rather than directly splitting desmosomes [J].
Aoyama, Y. ;
Nagai, M. ;
Kitajima, Y. .
BRITISH JOURNAL OF DERMATOLOGY, 2010, 162 (05) :1049-1055
[10]
A novel dominant mutation in plakoglobin causes Arrhythmogenic right ventricular cardiomyopathy [J].
Asimaki, Angeliki ;
Syrris, Petros ;
Wichter, Thomas ;
Matthias, Paul ;
Saffitz, Jeffrey E. ;
McKenna, William J. .
AMERICAN JOURNAL OF HUMAN GENETICS, 2007, 81 (05) :964-973