Autophagy Contributes to the Maintenance of Genomic Integrity by Reducing Oxidative Stress

• Published in: Oxidative medicine and cellular longevity Vol. 2020; no. 2020; pp. 1 - 14
• Main Authors: Shao, Changshun, Gong, Yaoqin, Zhang, Xiyu, Liu, Qiao, Wang, Jing, Yang, Tingting, Hao, Xiaohe, Bu, Wenqing, Li, Xi
• Format: Journal Article
• Language: English
• Published: Cairo, Egypt Hindawi Publishing Corporation 2020; Hindawi; Hindawi Limited
• Subjects: Antibodies; Antioxidants - pharmacology; Autophagy; Autophagy - drug effects; Autophagy - genetics; Cancer; Cell division; Cell Line, Tumor; Cellular Senescence - drug effects; Checkpoint Kinase 1 - metabolism; Deoxyribonucleic acid; DNA; DNA damage; Flow cytometry; Genomes; Genomic Instability - drug effects; Homeostasis; Humans; Mesenchymal Stem Cells - drug effects; Mesenchymal Stem Cells - metabolism; Micronuclei, Chromosome-Defective; Mutagens - toxicity; Oxidative stress; Oxidative Stress - drug effects; Oxidative Stress - genetics; Reactive Oxygen Species - metabolism; Sirolimus - pharmacology; Stem cells; United States > US; China
• ISSN: 1942-0900; 1942-0994
• DOI: 10.1155/2020/2015920

Autophagy has been well documented to play an important role in maintaining genomic stability. However, in addition to directly engulfing and digesting the damaged organelles and chromatin fragments, autophagy can affect many cellular processes including DNA damage response, regulation of redox homeostasis, and cell division; it remains to be determined to what extent each of those processes contributes to the maintenance of genomic stability. We here examined the role of autophagy-dependent redox regulation in the maintenance of genomic stability in two cancer cell lines (HT1080 and U2OS) and mesenchymal stem cells (MSCs) using micronuclei MN, also referred to as cytoplasmic chromatin fragments, as a marker. Our results showed that the spontaneous and genotoxic stress-induced frequencies of MN in cancer cells were significantly reduced by autophagy activators rapamycin and Torin1, and the reduction in MN was accompanied by a reduction in reactive oxygen species (ROS). Increased micronucleation in senescent MSCs, in which autophagic flux is blocked, was also attenuated by rapamycin, together with a reduction in ROS. Inhibition of autophagy by chloroquine (CQ) or ATG5 depletion, on the other hand, resulted in an increased frequency of MN, though a ROS elevation in response to autophagy inhibition was only observed in MSCs. Importantly, the induction of MN by autophagy inhibition in MSCs could be abrogated by antioxidant N-acetylcysteine (NAC). In contrast to the reported impairment of CHK1 activation in Atg7-deficient mouse embryonic fibroblasts, we found that the level of phosphorylated CHK1 was increased by CQ or ATG5 depletion but decreased by rapamycin or Torin1, suggesting that the increased genomic instability by defective autophagy is not caused by insufficient activation of CHK1-homologous recombination cascade. Together, our findings suggest that redox homeostasis regulated by autophagy contributes substantially to the maintenance of genomic stability in certain contexts.