Experimental Human Cell and Tissue Models of Pemphigus

被引:12
作者
van der Wier, Gerda [1 ]
Pas, Hendri H. [1 ]
Jonkman, Marcel F. [1 ]
机构
[1] Univ Groningen, Univ Med Ctr Groningen, Ctr Blistering Dis, Dept Dermatol, Hanzeplein 1,POB 30001, NL-9700 RB Groningen, Netherlands
关键词
D O I
10.1155/2010/143871
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Pemphigus is a chronic mucocutaneous autoimmune bullous disease that is characterized by loss of cell-cell contact in skin and/or mucous membranes. Past research has successfully identified desmosomes as immunological targets and has demonstrated that acantholysis is initiated through direct binding of IgG. The exact mechanisms of acantholysis, however, are still missing. Experimental model systems have contributed considerably to today's knowledge and are still a favourite tool of research. In this paper we will describe to what extent human cell and tissue models represent the in vivo situation, for example, organ cultures of human skin, keratinocyte cultures, and human skin grafted on mice and, furthermore, how suitable they are to study the pathogenesis of pemphigus. Organ cultures closely mimic the architecture of the epidermis but are less suitable to answer posed biochemical questions. Cultured keratinocyte monolayers are convenient in this respect, but their desmosomal make-up in terms of adhesion molecules does not exactly reflect the in vivo situation. Reconstituted skin is a relatively new model that approaches organ culture. In models of human skin grafted on mice, acantholysis can be studied in actual human skin but now with all the advantages of an animal model.
引用
收藏
页数:8
相关论文
共 64 条
[1]   Pemphigus vulgaris IgG causes a rapid depletion of desmoglein 3 (Dsg3) from the Triton X-100 soluble pools, leading to the formation of Dsg3-depleted desmosomes in a human squamous carcinoma cell line, DJM-1 cells [J].
Aoyama, Y ;
Kitajima, Y .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1999, 112 (01) :67-71
[2]   HUMAN-EPIDERMIS RECONSTRUCTED BY CULTURE - IS IT NORMAL [J].
ASSELINEAU, D ;
BERNARD, BA ;
BAILLY, C ;
DARMON, M ;
PRUNIERAS, M .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1986, 86 (02) :181-186
[3]   Pemphigus serum and captopril induce heat shock protein 70 and inducible nitric oxide synthase overexpression, triggering apoptosis in human keratinocytes [J].
Baroni, A ;
Buommino, E ;
Paoletti, I ;
Orlando, M ;
Ruocco, E ;
Ruocco, V .
BRITISH JOURNAL OF DERMATOLOGY, 2004, 150 (06) :1070-1080
[4]   Desmosome signaling - Inhibition of p38MAPK prevents pemphigus vulgaris IgG-induced cytoskeleton reorganization [J].
Berkowitz, P ;
Hu, PQ ;
Liu, Z ;
Diaz, LA ;
Enghild, JJ ;
Chua, MP ;
Rubenstein, DS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (25) :23778-23784
[5]  
BEUTNER EH, 1964, P SOC EXP BIOL MED, V117, P505
[6]   A novel explanation for acantholysis in pemphigus vulgaris: The basal cell shrinkage hypothesis [J].
Bystryn, JC ;
Grando, SA .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2006, 54 (03) :513-516
[7]   Desmoglein endocytosis and desmosome disassembly are coordinated responses to pemphigus autoantibodies [J].
Calkins, CC ;
Setzer, SV ;
Jennings, JM ;
Summers, S ;
Tsunoda, K ;
Amagai, M ;
Kowalczyk, AP .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (11) :7623-7634
[8]   Desmoglein versus non-desmoglein signaling in pemphigus acantholysis -: Characterization of novel signaling pathways downstream of pemphigus vulgaris antigens [J].
Chernyavsky, Alex I. ;
Arredondo, Juan ;
Kitajima, Yasuo ;
Sato-Nagai, Miki ;
Grando, Sergei A. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (18) :13804-13812
[9]   Cleavage of desmoglein 3 can explain its depletion from keratinocytes in pemphigus vulgaris [J].
Cirillo, Nicola ;
Campisi, Giuseppina ;
Gombos, Fernando ;
Perillo, Letizia ;
Femiano, Felice ;
Lanza, Alessandro .
EXPERIMENTAL DERMATOLOGY, 2008, 17 (10) :858-863
[10]   If pemphigus vulgaris IgG are the cause of acantholysis, new IgG-Independent mechanisms are the concause [J].
Cirillo, Nicola ;
Lanza, Michele ;
Femiano, Felice ;
Gaeta, Giovanni Maria ;
De Rosa, Alfredo ;
Gombos, Fernando ;
Lanza, Alessandro .
JOURNAL OF CELLULAR PHYSIOLOGY, 2007, 212 (03) :563-567