Synergistic Bcl-2 inhibition by ABT-737 and cyclosporine A

被引:10
作者
Cippa, Pietro E. [1 ,2 ]
Kamarashev, Jivko [3 ]
Chen, Jin [1 ,2 ]
Kraus, Anna K. [1 ,2 ]
Segerer, Stephan [2 ,4 ]
Feldmeyer, Laurence [3 ]
Fehr, Thomas [1 ,2 ]
机构
[1] Univ Zurich, Inst Physiol, Zurich, Switzerland
[2] Univ Zurich Hosp, Div Nephrol, CH-8091 Zurich, Switzerland
[3] Univ Zurich Hosp, Dept Dermatol, CH-8091 Zurich, Switzerland
[4] Univ Zurich, Dept Anat, Zurich, Switzerland
基金
瑞士国家科学基金会;
关键词
Bcl-2; ABT-737; Calcineurin; Cyclosporine A; Lymphocyte; Melanocyte; FAMILY ANTAGONIST ABT-737; T-LYMPHOCYTES; BCL-2-DEFICIENT MICE; CELL-DEATH; APOPTOSIS; CALCINEURIN; HOMEOSTASIS; MECHANISMS; RESISTANCE; PROTEINS;
D O I
10.1007/s10495-012-0778-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Survival of lymphocytes and melanocyte stem cells critically depends on B cell lymphoma 2 (Bcl-2). In T lymphocytes, a basal calcineurin activity maintains Bcl-2 expression in na < ve cells, and the activation of the calcineurin pathway orchestrates the regulation of the intrinsic apoptosis pathway after antigen recognition. Therefore, calcineurin inhibitors might potentiate the pro-apoptotic effect of pharmacological Bcl-2 inhibitors on lymphatic cells. In vitro, a reduced Bcl-2 expression in lymphocytes exposed to calcineurin inhibitors increased their sensitivity to the small molecule Bcl-2 inhibitor ABT-737. This correlated with an augmented pro-apoptotic activity of ABT-737 on lymphocytes in combination with cyclosporine A in na < ve mice in vivo. Interestingly, similar processes were observed in melanocytes. ABT-737 induced a fur depigmentation at the site of injection, and this effect was expanded to a generalized depigmentation in combination with cyclosporine A. Thus, inhibiting calcineurin increases the pro-apoptotic potency of ABT-737 in cells depending on Bcl-2 for survival. The increased efficacy of Bcl-2 inhibitors in combination with cyclosporine A might be relevant to exploit their anti-neoplastic and immuno-modulatory properties.
引用
收藏
页码:315 / 323
页数:9
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