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活性氧非依赖的线粒体途径参与棉酚诱导的细胞凋亡

Involvement of reactive oxygen species-independent mitochondrial pathway in gossypol-induced apoptosis.

作者信息

Hou De-Xing, Uto Takuhiro, Tong Xuhui, Takeshita Toru, Tanigawa Shunsuke, Imamura Izumi, Ose Takashi, Fujii Makoto

机构信息

Department of Biochemical Science and Technology, Faculty of Agriculture, Kagoshima University, Korimoto 1-21-24, Kagoshima 890-0065, Japan.

出版信息

Arch Biochem Biophys. 2004 Aug 15;428(2):179-87. doi: 10.1016/j.abb.2004.06.007.

Abstract

Gossypol is a component present in cottonseeds and has been demonstrated to be an effective contraceptive drug in preventing spermatogenesis in mammalian species. In the present, we reported that gossypol could induce apoptosis in human promyelocytic leukemia cells (HL-60), as characterized by DNA fragmentation, poly(ADP) ribose polymerase (PARP) cleavage. The efficacious induction of apoptosis was observed at 50 microM for 6 h. Further molecular analysis showed that gossypol induced the truncation of Bid protein, the loss of mitochondrial membrane potential (DeltaPsi m), cytochrome c release from mitochondria into cytosol, and activation of caspase-3, -8, and -9. However, gossypol did not increase the level of reactive oxygen species (ROS), and antioxidants including N-acetyl cysteine (NAC) and catalase could not block gossypol-induced apoptosis in the HL-60 cells. These data suggest that gossypol induces apoptosis in HL-60 cells through ROS-independent mitochondrial dysfunction pathway.

摘要

棉酚是棉籽中的一种成分,已被证明是一种有效的避孕药物,可阻止哺乳动物物种的精子发生。在本研究中,我们报道棉酚可诱导人早幼粒细胞白血病细胞(HL-60)凋亡,其特征为DNA片段化、聚(ADP)核糖聚合酶(PARP)裂解。在50微摩尔浓度下作用6小时可观察到有效的凋亡诱导。进一步的分子分析表明,棉酚诱导Bid蛋白截断、线粒体膜电位(ΔΨm)丧失、细胞色素c从线粒体释放到细胞质中以及半胱天冬酶-3、-8和-9的激活。然而,棉酚并未增加活性氧(ROS)水平,包括N-乙酰半胱氨酸(NAC)和过氧化氢酶在内的抗氧化剂不能阻断棉酚诱导的HL-60细胞凋亡。这些数据表明,棉酚通过不依赖ROS的线粒体功能障碍途径诱导HL-60细胞凋亡。

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