Fas ligand in pemphigus sera induces keratinocyte apoptosis through the activation of caspase-8

被引:109
作者
Puviani, M
Marconi, A
Cozzani, E
Pincelli, C
机构
[1] Univ Modena & Reggio Emilia, Dermatol Sect, Dept Internal Med, I-41100 Modena, Italy
[2] Univ Genoa, Inst Dermatol, Genoa, Italy
关键词
acantholysis; anoikis; corticosteroids; Fas;
D O I
10.1046/j.1523-1747.2003.12014.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
The Fas/Fas ligand system triggers the extrinsic apoptotic pathway and is involved in several inflammatory conditions, also at the skin level. The Fas/Fas ligand cell death pathway plays a major role in anoikis, a type of apoptosis characterized by cell detachment. As pemphigus is characterized by loss of cell to cell adhesion, we evaluated the role of anoikis and Fas ligand in this bullous disease. We report that, in suprabasal epidermis from perilesional pemphigus skin, most keratinocytes are apoptotic. Moreover, Fas ligand levels are markedly increased in sera from pemphigus patients, whereas they are undetectable in sera from patients undergoing steroid treatment. Sera from untreated patients but not from patients under steroids induce keratinocyte apoptosis. Pemphigus-sera-induced cell death is partially inhibited by pretreatment with anti-Fas ligand antibodies and by incubation with caspase-8 inhibitor Z-IETD-FMK. Finally, caspase-8 is activated in keratinocytes provided with sera from pemphigus patients, whereas cleavage is partially blocked by pretreatment of sera with anti-Fas ligand antibody. These results suggest that increased Fas ligand in pemphigus sera is responsible for keratinocyte apoptosis, which occurs through the activation of a caspase-8-driven extrinsic apoptotic pathway.
引用
收藏
页码:164 / 167
页数:4
相关论文
共 24 条
[1]   Matrix attachment regulates Fas-induced apoptosis in endothelial cells: A role for c-Flip and implications for anoikis [J].
Aoudjit, F ;
Vuori, K .
JOURNAL OF CELL BIOLOGY, 2001, 152 (03) :633-643
[2]   Elevated serum level of Fas ligand correlates with the asymptomatic stage of human immunodeficiency virus infection [J].
Bahr, GM ;
Capron, A ;
Dewulf, J ;
Nagata, S ;
Tanaka, M ;
Bourez, JM ;
Mouton, Y .
BLOOD, 1997, 90 (02) :896-898
[3]   Mouse proximal tubular cell-cell adhesion inhibits apoptosis by a cadherin-dependent mechanism [J].
Bergin, E ;
Levine, JS ;
Koh, JS ;
Lieberthal, W .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2000, 278 (05) :F758-F768
[4]   DISRUPTION OF EPITHELIAL CELL-MATRIX INTERACTIONS INDUCES APOPTOSIS [J].
FRISCH, SM ;
FRANCIS, H .
JOURNAL OF CELL BIOLOGY, 1994, 124 (04) :619-626
[5]   Evidence for a function of death-receptor-related, death-domain-containing proteins in anoikis [J].
Frisch, SM .
CURRENT BIOLOGY, 1999, 9 (18) :1047-1049
[6]   Anoikis mechanisms [J].
Frisch, SM ;
Screaton, RA .
CURRENT OPINION IN CELL BIOLOGY, 2001, 13 (05) :555-562
[7]   Transduction - Integrin signaling [J].
Giancotti, FG ;
Ruoslahti, E .
SCIENCE, 1999, 285 (5430) :1028-1032
[8]   Relationship between keratinocyte adhesion and death: anoikis in acantholytic diseases [J].
Gniadecki, R ;
Jemec, GBE ;
Thomsen, BM ;
Hansen, M .
ARCHIVES OF DERMATOLOGICAL RESEARCH, 1998, 290 (10) :528-532
[9]  
Grossmann J, 2001, CELL GROWTH DIFFER, V12, P147
[10]   Essential requirement for caspase-8/FLICE in the initiation of the Fas-induced apoptotic cascade [J].
Juo, P ;
Kuo, CJ ;
Yuan, JY ;
Blenis, J .
CURRENT BIOLOGY, 1998, 8 (18) :1001-1008