CTLA-4-/- mice display T cell-apoptosis resistance resembling that ascribed to autoimmune-prone non-obese diabetic (NOD) mice

被引:32
作者
Bergman, ML
Cilio, CM
Penha-Gonçalves, C
Lamhamedi-Cherradi, SE
Löfgren, A
Colucci, F
Lejon, K
Garchon, HJ
Holmberg, D [1 ]
机构
[1] Umea Univ, Umea Ctr Mol Med, S-90187 Umea, Sweden
[2] Umea Univ, Dept Cell & Mol Biol, S-90187 Umea, Sweden
[3] Gulbenkian Inst Sci, P-2780 Oeiras, Portugal
[4] Hop Necker Enfants Malad, INSERM, U25, F-75743 Paris, France
关键词
gamma-irradiation; apoptosis; costimulation; autoimmunity; type; 1; diabetes;
D O I
10.1006/jaut.2000.0474
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The genes conferring susceptibility to autoimmune (insulin-dependent) diabetes mellitus (IDDM) are, in most cases, not defined. Among the loci so far identified as associated with murine IDDM (Idd1-19), only the nature of Idd1 has been assessed. Here we show that thymocytes and peripheral lymphocytes of the non-obese diabetic (NOD) mouse are relatively resistant to apoptosis induced by gamma -irradiation. By linkage analysis of F2 progeny mice, we map this trait to a locus on chromosome 1 containing the Idd5 diabetes susceptibility region. By the use of congenic mice, we confirm the linkage data and map this locus to a 6 cM region on proximal chromosome 1. Ctla4, being localized in this chromosomal region and mediating crucial functions in T cell biology, is a logical candidate gene in the Idd5 susceptibility region. In line with this, we demonstrate that T cells from Ctla4(-/-) deficient mice show a similar resistance to gamma -irradiation-induced apoptosis as observed in the NOD mice. This reinforces the notion that CTLA-4 contributes to the pathogenesis of autoimmune diabetes. (C) 2001 Academic Press.
引用
收藏
页码:105 / 113
页数:9
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