Proapoptotic Bcl-2 Relative Bim Required for Certain Apoptotic Responses, Leukocyte Homeostasis, and to Preclude Autoimmunity

Philippe Bouillet(Walter and Eliza Hall Institute of Medical Research), Donald Metcalf(Walter and Eliza Hall Institute of Medical Research), David C.S. Huang(Walter and Eliza Hall Institute of Medical Research), David M. Tarlinton(Walter and Eliza Hall Institute of Medical Research), Tom Kay(Walter and Eliza Hall Institute of Medical Research), Frank Köntgen(Walter and Eliza Hall Institute of Medical Research), Jerry M. Adams(Walter and Eliza Hall Institute of Medical Research), Andreas Strasser(Walter and Eliza Hall Institute of Medical Research)
Science
November 26, 1999
Cited by 1,497

Abstract

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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