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Mechanism of mitochondrial membrane permeabilization during apoptosis under Photofrin-mediated photodynamic therapy

机译:光敏蛋白介导的光动力疗法在细胞凋亡过程中线粒体膜通透性的机制

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摘要

Photofrin-mediated photodynamic therapy (PF-PDT) can induce cell apoptosis via the mitochondria/caspase-3 pathway. Here, we further investigate the mechanism involved in the mitochondrial apoptotic process induced by PF-PDT. A high-level intracellular reactive oxygen species (ROS) generation in mitochondria, mitochondrial swelling, and dissipation of mitochondrial transmembrane potential were observed immediately after irradiation, indicating that mitochondria were the major ROS generation sites and also the first oxidative damage sites after PF-PDT treatment. For mitochondrial permeability detection, the decrease of calcein fluorescence emission intensity and release of cytochrome c were observed immediately after PF-PDT treatment, indicating the occurrence of mitochondrial inner membrane permeabilization (MIMP) and the mitochondrial outer membrane permeabilization (MOMP). However, cytochrome c release was not prevented by cyclosporine (CsA), a specific inhibitor of mitochondrial permeability transition (MPT). Taken together, these results demonstrated that PF-PDT caused simultaneous onset of MIMP and MOMP immediately after the treatment, and MOMP was independent of the MPT. Besides, inducible mitochondrial ROS generation played key roles in PF-PDT-induced cell apoptosis. This study will be benefit for understanding the mechanism involved in the initial mitochondrial oxidative damage by PF-PDT.
机译:Photofrin介导的光动力疗法(PF-PDT)可以通过线粒体/ caspase-3途径诱导细胞凋亡。在这里,我们进一步调查参与PF-PDT诱导线粒体凋亡过程的机制。照射后立即观察到线粒体中高水平的细胞内活性氧(ROS)生成,线粒体肿胀和线粒体跨膜电位的耗散,这表明线粒体是主要的ROS生成位点,也是PF-PDT之后的第一个氧化损伤位点治疗。对于线粒体通透性检测,PF-PDT处理后立即观察到钙黄绿素荧光发射强度的降低和细胞色素c的释放,表明线粒体内膜通透性(MIMP)和线粒体外膜通透性(MOMP)的发生。但是,细胞色素c的释放并没有被环孢素(CsA)阻止,后者是线粒体通透性转变(MPT)的特异性抑制剂。综上所述,这些结果表明PF-PDT在治疗后立即引起MIMP和MOMP的同时发作,并且MOMP独立于MPT。此外,诱导型线粒体ROS的产生在PF-PDT诱导的细胞凋亡中起关键作用。这项研究将有助于了解PF-PDT引起的初始线粒体氧化损伤的机制。

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