The majority of lamina propria CD4+ T-cells from scid mice with colitis undergo Fas-mediated apoptosis in vivo

被引:9
作者
Bregenholt, S [1 ]
Petersen, TR [1 ]
Claesson, MH [1 ]
机构
[1] Univ Copenhagen, Panum Inst, Dept Med Anat, Expt Immunol Lab, DK-2200 Copenhagen N, Denmark
关键词
Fas; apoptosis; colitis; scid mice; mucosal immunity;
D O I
10.1016/S0165-2478(01)00240-1
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We have previously shown that adoptively transferred CD4(+) T-cells mediate an chronic colitis in severe combined immune deficient (scid) mice. Colitis is accompanied by activation and apoptosis of Fas ligand and TNF-alpha expressing CD4(+) T-cells in the diseased colonic lamina propria (Eur. J. Immunol. 28:3655 (1998)). Here we investigate the apoptosis-inducing mechanism in these lamina propria infiltrating CD4(+) T-cells. We observe that freshly isolated lamina propria CD4(+) T-cells can kill Fas transfected P815 mastocytoma cells in a TCR/CD3 redirected chromium-release assay, but do not express TNF-a mediated cytotoxicity. Pre-incubation of the isolated lamina propria CD4(+) T-cells with an anti-FasL antiserum partially blocked killing of the Fas transfected target cells, indicating a role for the Fas-FasL system in the killing process. Treatment of scid mice with colitis with anti-FasL antiserum for 12 h blocked the apoptotic process in lamina propria CD4(+) T-cells by more than 65%,, compared to mice treated with control antiserum. Together, these results point towards the Fas-FasL and not the TNF-alpha -TNF-alpha receptor system as the primary apoptosis-inducing mechanism of lamina propria CD4(+) T-cells in this model of murine chronic colitis, and suggest an important role for the Fas-FasL system in the maintenance of homeostasis of locally proliferating T-cells. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:7 / 12
页数:6
相关论文
共 28 条
[1]   Cellular environments and apoptosis: Tissue microenvironments control activated T-cell death [J].
Akbar, AN ;
Salmon, M .
IMMUNOLOGY TODAY, 1997, 18 (02) :72-76
[2]   Oral administration of recombinant cholera toxin subunit B inhibits IL-12-mediated murine experimental (trinitrobenzene sulfonic acid) colitis [J].
Boirivant, M ;
Fuss, IJ ;
Ferroni, L ;
De Pascale, M ;
Strober, W .
JOURNAL OF IMMUNOLOGY, 2001, 166 (05) :3522-3532
[3]   REGIONAL SPECIALIZATION OF INTRAEPITHELIAL T-CELLS IN THE MURINE SMALL AND LARGE-INTESTINE [J].
BOLL, G ;
RUDOLPHI, A ;
SPIESS, S ;
REIMANN, J .
SCANDINAVIAN JOURNAL OF IMMUNOLOGY, 1995, 41 (02) :103-113
[4]   Cytotoxic reactivity of gut lamina propria CD4(+) alpha beta T cells in SCID mice, with colitis [J].
Bonhagen, K ;
Thoma, S ;
Bland, P ;
Bregenholt, S ;
Rudolphi, A ;
Claesson, MH ;
Reimann, J .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1996, 26 (12) :3074-3083
[5]  
Bonhagen K, 1998, CLIN EXP IMMUNOL, V112, P443
[6]  
Bregenholt S, 1996, J IMMUNOL, V157, P993
[7]   Cells and cytokines in the pathogenesis of inflammatory bowel disease: New insights from mouse T cell transfer models [J].
Bregenholt, S .
EXPERIMENTAL AND CLINICAL IMMUNOGENETICS, 2000, 17 (03) :115-129
[8]   T-cell transfer and cytokine/TCR gene deletion models in the study of inflammatory bowel disease [J].
Bregenholt, S ;
Delbro, D ;
Claesson, MH .
APMIS, 1997, 105 (09) :655-662
[9]  
Bregenholt S, 1998, CLIN EXP IMMUNOL, V114, P19
[10]  
Bregenholt S, 1998, EUR J IMMUNOL, V28, P3655, DOI 10.1002/(SICI)1521-4141(199811)28:11<3655::AID-IMMU3655>3.0.CO