Ježek Jan, Cooper Katrina F, Strich Randy
Department of Molecular Biology, Rowan University Graduate School of Biomedical Sciences, Stratford, NJ 08084, USA.
Antioxidants (Basel). 2018 Jan 16;7(1):13. doi: 10.3390/antiox7010013.
Mitochondria are organelles with a highly dynamic ultrastructure maintained by a delicate equilibrium between its fission and fusion rates. Understanding the factors influencing this balance is important as perturbations to mitochondrial dynamics can result in pathological states. As a terminal site of nutrient oxidation for the cell, mitochondrial powerhouses harness energy in the form of ATP in a process driven by the electron transport chain. Contemporaneously, electrons translocated within the electron transport chain undergo spontaneous side reactions with oxygen, giving rise to superoxide and a variety of other downstream reactive oxygen species (ROS). Mitochondrially-derived ROS can mediate redox signaling or, in excess, cause cell injury and even cell death. Recent evidence suggests that mitochondrial ultrastructure is tightly coupled to ROS generation depending on the physiological status of the cell. Yet, the mechanism by which changes in mitochondrial shape modulate mitochondrial function and redox homeostasis is less clear. Aberrant mitochondrial morphology may lead to enhanced ROS formation, which, in turn, may deteriorate mitochondrial health and further exacerbate oxidative stress in a self-perpetuating vicious cycle. Here, we review the latest findings on the intricate relationship between mitochondrial dynamics and ROS production, focusing mainly on its role in malignant disease.
线粒体是具有高度动态超微结构的细胞器,其裂变和融合速率之间的微妙平衡维持着这种结构。了解影响这种平衡的因素很重要,因为线粒体动力学的扰动可能导致病理状态。作为细胞营养物质氧化的终端场所,线粒体动力工厂在电子传递链驱动的过程中以ATP的形式获取能量。同时,在电子传递链中转移的电子会与氧气发生自发的副反应,产生超氧化物和各种其他下游活性氧(ROS)。线粒体衍生的ROS可以介导氧化还原信号传导,或者过量时会导致细胞损伤甚至细胞死亡。最近的证据表明,线粒体超微结构根据细胞的生理状态与ROS生成紧密相关。然而,线粒体形态变化调节线粒体功能和氧化还原稳态的机制尚不清楚。异常的线粒体形态可能导致ROS形成增加,进而可能使线粒体健康恶化,并在自我延续的恶性循环中进一步加剧氧化应激。在这里,我们综述了关于线粒体动力学与ROS产生之间复杂关系的最新发现,主要关注其在恶性疾病中的作用。