Mammalian cells evacuate and shelter mitochondrial DNA from destruction following hypoxia response-induced mitophagy

Abstract

Cells use a specialized process called mitophagy to degrade mitochondria, and the conditions that induce mitophagy can endanger mitochondrial DNA (mtDNA). Here, we report a novel mechanism by which cells undergoing hypoxia response (HR)-induced mitophagy protect their mtDNA from destruction by segregating it into large mitochondria (Mito-L). Using time-lapse imaging, we found that Mito-L are formed when mitochondria undergo tubular-to-spherical transitions and then fuse together. Under HR-activating conditions, we found the mitophagy process itself is essential for Mito-L formation. When we fragmented mitochondria prior to inducing the HR, we observed fewer Mito-L and more mtDNA degradation. Thus, mammalian cells protect mtDNA against excessive mitophagy induced by HR, thereby preventing the loss of the genetic information. Hypoxia response-induced mitophagy triggers cells to shelter mitochondrial DNA (70 characters)