Dendritic cell apoptosis in the maintenance of immune tolerance

被引:272
作者
Chen, M [1 ]
Wang, YH
Wang, YH
Huang, L
Sandoval, H
Liu, YJ
Wang, J
机构
[1] Baylor Coll Med, Dept Immunol, Houston, TX 77030 USA
[2] Univ Texas, MD Anderson Canc Ctr, Dept Immunol, Houston, TX 77030 USA
关键词
D O I
10.1126/science.1122545
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
Apoptosis in the immune system is critical for maintaining self-tolerance and preventing autoimmunity. Nevertheless, inhibiting apoptosis in lymphocytes is not alone sufficient to break self-tolerance, suggesting the involvement of other cell types. We investigated whether apoptosis in dendritic cells (DCs) helps regulate self-tolerance by generating transgenic mice expressing the baculoviral caspase inhibitor, p35, in DCs (DC-p35). DC-p35 mice displayed defective DC apoptosis, resulting in their accumulation and, in turn, chronic lymphocyte activation and systemic autoimmune manifestations. The observation that a defect in DC apoptosis can independently lead to autoimmunity is consistent with a central rote for these cells in maintaining immune self-tolerance.
引用
收藏
页码:1160 / 1164
页数:5
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