Department of Surgery, Washington University in St. Louis, St. Louis, MO 63110, USA.
Department of Cell Biology & Physiology, Washington University in St. Louis, St. Louis, MO 63110, USA.
Cells. 2022 Dec 16;11(24):4083. doi: 10.3390/cells11244083.
Mitochondrial autophagy (mitophagy) is a central catabolic event for mitochondrial quality control. Defective or insufficient mitophagy, thus, can result in mitochondrial dysfunction, and ultimately cell death. There is a strong causal relationship between ischemia/reperfusion (I/R) injury and mitochondrial dysfunction following liver resection and transplantation. Compared to young patients, elderly patients poorly tolerate I/R injury. Accumulation of abnormal mitochondria after I/R is more prominent in aged livers than in young counterparts. This review highlights how altered autophagy is mechanistically involved in age-dependent hypersensitivity to reperfusion injury.
线粒体自噬(mitophagy)是线粒体质量控制的核心分解事件。因此,线粒体自噬功能缺陷或不足可导致线粒体功能障碍,并最终导致细胞死亡。肝切除和肝移植后缺血/再灌注(I/R)损伤与线粒体功能障碍之间存在着很强的因果关系。与年轻患者相比,老年患者对 I/R 损伤的耐受性较差。与年轻供体相比,I/R 后异常线粒体在老年供体肝脏中的积累更为明显。本综述强调了自噬改变如何在机制上参与了与年龄相关的再灌注损伤的超敏反应。