De Gaetano Anna, Gibellini Lara, Zanini Giada, Nasi Milena, Cossarizza Andrea, Pinti Marcello
Department of Life Sciences, University of Modena and Reggio Emilia, 41125 Modena, Italy.
Department of Medical and Surgical Sciences of Children and Adults, University of Modena and Reggio Emilia, 41125 Modena, Italy.
Antioxidants (Basel). 2021 May 17;10(5):794. doi: 10.3390/antiox10050794.
Mitochondrial dysfunction is a hallmark of aging. Dysfunctional mitochondria are recognized and degraded by a selective type of macroautophagy, named mitophagy. One of the main factors contributing to aging is oxidative stress, and one of the early responses to excessive reactive oxygen species (ROS) production is the induction of mitophagy to remove damaged mitochondria. However, mitochondrial damage caused at least in part by chronic oxidative stress can accumulate, and autophagic and mitophagic pathways can become overwhelmed. The imbalance of the delicate equilibrium among mitophagy, ROS production and mitochondrial damage can start, drive, or accelerate the aging process, either in physiological aging, or in pathological age-related conditions, such as Alzheimer's and Parkinson's diseases. It remains to be determined which is the prime mover of this imbalance, i.e., whether it is the mitochondrial damage caused by ROS that initiates the dysregulation of mitophagy, thus activating a vicious circle that leads to the reduced ability to remove damaged mitochondria, or an alteration in the regulation of mitophagy leading to the excessive production of ROS by damaged mitochondria.
线粒体功能障碍是衰老的一个标志。功能失调的线粒体通过一种名为线粒体自噬的选择性巨自噬类型被识别并降解。导致衰老的主要因素之一是氧化应激,对过量活性氧(ROS)产生的早期反应之一是诱导线粒体自噬以清除受损的线粒体。然而,至少部分由慢性氧化应激引起的线粒体损伤会积累,并且自噬和线粒体自噬途径可能不堪重负。线粒体自噬、ROS产生和线粒体损伤之间微妙平衡的失衡可以在生理衰老或与年龄相关的病理状况(如阿尔茨海默病和帕金森病)中启动、驱动或加速衰老过程。尚有待确定这种失衡的主要推动者是什么,即是否是由ROS引起的线粒体损伤引发了线粒体自噬的失调,从而激活一个恶性循环,导致清除受损线粒体的能力下降,还是线粒体自噬调节的改变导致受损线粒体过度产生ROS。