自身免疫
细胞凋亡
平衡
细胞生物学
造血
Bcl-2家族
生物
细胞因子
免疫学
程序性细胞死亡
干细胞
免疫系统
遗传学
作者
Philippe Bouillet,Donald Metcalf,David C.S. Huang,David M. Tarlinton,Tom Kay,Frank Köntgen,Jerry M. Adams,Andreas Strasser
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:1999-11-26
卷期号:286 (5445): 1735-1738
被引量:1498
标识
DOI:10.1126/science.286.5445.1735
摘要
Apoptosis can be triggered by members of the Bcl-2 protein family, such as Bim, that share only the BH3 domain with this family. Gene targeting in mice revealed important physiological roles for Bim. Lymphoid and myeloid cells accumulated, T cell development was perturbed, and most older mice accumulated plasma cells and succumbed to autoimmune kidney disease. Lymphocytes were refractory to apoptotic stimuli such as cytokine deprivation, calcium ion flux, and microtubule perturbation but not to others. Thus, Bim is required for hematopoietic homeostasis and as a barrier to autoimmunity. Moreover, particular death stimuli appear to activate apoptosis through distinct BH3-only proteins.
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