PUBLICATION

ROS signaling-induced mitochondrial Sgk1 expression regulates epithelial cell renewal

Authors
Li, Y., Liu, C., Rolling, L., Sikora, V., Chen, Z., Gurwin, J., Barabell, C., Lin, J., Duan, C.
ID
ZDB-PUB-230606-36
Date
2023
Source
Proceedings of the National Academy of Sciences of the United States of America   120: e2216310120e2216310120 (Journal)
Registered Authors
Duan, Cunming, Liu, Chengdong
Keywords
F1Fo-ATP synthase, IGF/insulin signaling, mitochondrial membrane potential, reactive oxygen species, serum- and glucocorticoid-regulated kinase 1
MeSH Terms
  • Adenosine Triphosphate/metabolism
  • Animals
  • Epithelial Cells/metabolism
  • Humans
  • Mitochondria*/genetics
  • Mitochondria*/metabolism
  • Reactive Oxygen Species/metabolism
  • Zebrafish*/genetics
  • Zebrafish*/metabolism
PubMed
37276417 Full text @ Proc. Natl. Acad. Sci. USA
Abstract
Many types of differentiated cells can reenter the cell cycle upon injury or stress. The underlying mechanisms are still poorly understood. Here, we investigated how quiescent cells are reactivated using a zebrafish model, in which a population of differentiated epithelial cells are reactivated under a physiological context. A robust and sustained increase in mitochondrial membrane potential was observed in the reactivated cells. Genetic and pharmacological perturbations show that elevated mitochondrial metabolism and ATP synthesis are critical for cell reactivation. Further analyses showed that elevated mitochondrial metabolism increases mitochondrial ROS levels, which induces Sgk1 expression in the mitochondria. Genetic deletion and inhibition of Sgk1 in zebrafish abolished epithelial cell reactivation. Similarly, ROS-dependent mitochondrial expression of SGK1 promotes S phase entry in human breast cancer cells. Mechanistically, SGK1 coordinates mitochondrial activity with ATP synthesis by phosphorylating F1Fo-ATP synthase. These findings suggest a conserved intramitochondrial signaling loop regulating epithelial cell renewal.
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