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萝卜硫素(一种十字花科蔬菜来源的癌症化学预防剂)诱导细胞凋亡需要Bax和Bak。

Bax and Bak are required for apoptosis induction by sulforaphane, a cruciferous vegetable-derived cancer chemopreventive agent.

作者信息

Choi Sunga, Singh Shivendra V

机构信息

Department of Pharmacology and University of Pittsburgh Cancer Institute, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania 15213, USA.

出版信息

Cancer Res. 2005 Mar 1;65(5):2035-43. doi: 10.1158/0008-5472.CAN-04-3616.

Abstract

Sulforaphane, a constituent of many edible cruciferous vegetables, including broccoli, effectively suppresses proliferation of cancer cells in culture and in vivo by causing apoptosis induction, but the sequence of events leading to cell death is poorly defined. Here, we show that multidomain proapoptotic Bcl-2 family members Bax and Bak play a critical role in apoptosis induction by sulforaphane. This conclusion is based on the following observations: (a) sulforaphane treatment caused a dose- and time-dependent increase in the protein levels of both Bax and Bak and conformational change and mitochondrial translocation of Bax in SV40-transformed mouse embryonic fibroblasts (MEF) derived from wild-type mice to trigger cytosolic release of apoptogenic molecules (cytochrome c and Smac/DIABLO), activation of caspase-9 and caspase-3, and ultimately cell death; (b) MEFs derived from Bax or Bak knockout mice resisted cell death by sulforaphane, and (c) MEFs derived from Bax and Bak double knockout mice exhibited even greater protection against sulforaphane-induced cytochrome c release, caspase activation, and apoptosis compared with wild-type or single knockout cells. Interestingly, sulforaphane treatment also caused a dose- and time-dependent increase in the protein level of Apaf-1 in wild-type, Bax-/-, and Bak-/- MEFs but not in double knockout, suggesting that Bax and Bak might regulate sulforaphane-mediated induction of Apaf-1 protein. A marked decline in the protein level of X-linked inhibitor of apoptosis on treatment with sulforaphane was also observed. Thus, it is reasonable to postulate that sulforaphane-induced apoptosis is amplified by a decrease in X-linked inhibitor of apoptosis level, which functions to block cell death by inhibiting activities of caspases. In conclusion, the results of the present study indicate that Bax and Bak proteins play a critical role in initiation of cell death by sulforaphane.

摘要

萝卜硫素是包括西兰花在内的许多可食用十字花科蔬菜的一种成分,它通过诱导细胞凋亡有效地抑制培养细胞和体内癌细胞的增殖,但导致细胞死亡的一系列事件却鲜为人知。在此,我们表明多结构域促凋亡Bcl-2家族成员Bax和Bak在萝卜硫素诱导的细胞凋亡中起关键作用。这一结论基于以下观察结果:(a) 萝卜硫素处理导致野生型小鼠来源的SV40转化小鼠胚胎成纤维细胞(MEF)中Bax和Bak的蛋白水平呈剂量和时间依赖性增加,Bax发生构象变化并转位至线粒体,从而触发凋亡分子(细胞色素c和Smac/DIABLO)的胞质释放,激活caspase-9和caspase-3,最终导致细胞死亡;(b) Bax或Bak基因敲除小鼠来源的MEF对萝卜硫素诱导的细胞死亡具有抗性;(c) 与野生型或单基因敲除细胞相比,Bax和Bak双基因敲除小鼠来源的MEF对萝卜硫素诱导的细胞色素c释放、caspase激活和细胞凋亡具有更强的抗性。有趣的是,萝卜硫素处理还导致野生型、Bax-/-和Bak-/- MEF中Apaf-1的蛋白水平呈剂量和时间依赖性增加,但在双基因敲除细胞中未出现这种情况,这表明Bax和Bak可能调节萝卜硫素介导的Apaf-1蛋白诱导。在用萝卜硫素处理后,还观察到X连锁凋亡抑制蛋白的蛋白水平显著下降。因此,合理的推测是,萝卜硫素诱导的细胞凋亡通过X连锁凋亡抑制蛋白水平的降低而被放大,X连锁凋亡抑制蛋白通过抑制caspase的活性来阻止细胞死亡。总之,本研究结果表明Bax和Bak蛋白在萝卜硫素引发的细胞死亡中起关键作用。

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