Apoptosis resistance of nonobese diabetic peripheral lymphocytes linked to the Idd5 diabetes susceptibility region

被引:97
作者
Colucci, F [1 ]
Bergman, ML [1 ]
PenhaGoncalves, C [1 ]
Cilio, CM [1 ]
Holmberg, D [1 ]
机构
[1] UMEA UNIV,DEPT CELL & MOL BIOL,S-90187 UMEA,SWEDEN
关键词
D O I
10.1073/pnas.94.16.8670
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Defects in lymphocyte apoptosis may lead to autoimmune disorders and contribute to the pathogenesis of type 1 diabetes. Lymphocytes of nonobese diabetic (NOD) mice, an animal model of autoimmune diabetes, hare been found resistant to various apoptosis signals, including the alkylating drug cyclophosphamide. Using an F-2 intercross between the apoptosis-resistant NOD mouse and the apoptosis-susceptible C57BL/6 mouse, we define a major locus controlling the apoptosis-resistance phenotype and demonstrate its linkage (logarithm of odds score = 3.9) to a group of medial markers on chromosome 1, The newly defined gene cannot be dissociated from Ctla4 and Cd28 and in fact marks a 20-centimorgan region encompassing Idd5, a previously postulated diabetes susceptibility locus, Interestingly, we find that the CTLA-4 (cytotoxic T lymphocyte-associated antigen 4) and the CD28 costimulatory molecules are defectively expressed in NOD mice, suggesting that one or both of these molecules may be involved in (he control of apoptosis resistance and, in turn, in diabetes susceptibility.
引用
收藏
页码:8670 / 8674
页数:5
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