Dubois Charlotte, Kondratskyi Artem, Bidaux Gabriel, Noyer Lucile, Vancauwenberghe Eric, Farfariello Valério, Toillon Robert-Allain, Roudbaraki Morad, Tierny Dominique, Bonnal Jean-Louis, Prevarskaya Natalia, Vanden Abeele Fabien
Univ. Lille, Inserm, U1003 - PHYCEL - Physiologie Cellulaire, 59000 Lille, France.
Univ. Lille, Inserm, U1003 - PHYCEL - Physiologie Cellulaire, 59000 Lille, France.
iScience. 2020 Jul 24;23(7):101263. doi: 10.1016/j.isci.2020.101263. Epub 2020 Jun 12.
Mitochondria are important cell death checkpoints, and mitochondrial Ca overload is considered as a potent apoptotic intrinsic pathway inducer. Here, we report that this Ca apoptosis link is largely ineffective in inducing cell-death just by itself and required a concomitant inhibition of autophagy to counteract its pro-survival action. In such condition, an acute mitochondrial stress revealed by a DRP1-mediated mitochondrial dynamic remodeling is observed concomitantly with mitochondrial depolarization, release of cytochrome c, and efficient apoptosis induction. We also uncover that mitochondrial Ca status modulates the function of autophagy as a sensitizer for chemotherapies. This priming mediated by mitochondrial Ca overload and inhibition of autophagy sensitizes many cancer cells types to different chemotherapies with independent mechanisms of action. Collectively, our results redefine an important cell signaling pathway, uncovering new combined therapies for the treatment of diseases associated with mitochondrial Ca homeostasis disorders such as cancer.
线粒体是重要的细胞死亡检查点,线粒体钙超载被认为是一种强大的凋亡内在途径诱导剂。在此,我们报告,这种钙凋亡联系仅靠自身在诱导细胞死亡方面大多无效,需要同时抑制自噬以抵消其促生存作用。在这种情况下,伴随着线粒体去极化、细胞色素c释放和有效的凋亡诱导,观察到由动力蛋白1(DRP1)介导的线粒体动态重塑所揭示的急性线粒体应激。我们还发现线粒体钙状态调节自噬作为化疗敏化剂的功能。由线粒体钙超载和自噬抑制介导的这种预处理使许多癌细胞类型对具有独立作用机制的不同化疗敏感。总体而言,我们的结果重新定义了一条重要的细胞信号通路,揭示了用于治疗与线粒体钙稳态紊乱相关疾病(如癌症)的新联合疗法。