Antioxidant defense in quiescent cells determines selectivity of electron transport chain inhibition-induced cell death

0481503 - BTÚ 2018 RIV US eng J - Článek v odborném periodiku
Blecha, Jan - Novais, Silvia Magalhaes - Rohlenová, Kateřina - Novotná, Eliška - Lettlová, Sandra - Schmitt, S. - Zischka, H. - Neužil, Jiří - Rohlena, Jakub
Antioxidant defense in quiescent cells determines selectivity of electron transport chain inhibition-induced cell death.
Free Radical Biology and Medicine. Roč. 112, NOV 2017 (2017), s. 253-266. ISSN 0891-5849. E-ISSN 1873-4596
Grant CEP: GA ČR GA16-22823S; GA ČR GA17-20904S; GA ČR GA16-12719S; GA MZd(CZ) NV16-31604A; GA MŠMT(CZ) LM2015062; GA MŠMT(CZ) LQ1604; GA MŠMT(CZ) ED1.1.00/02.0109
Institucionální podpora: RVO:86652036
Klíčová slova: Electron transport chain * Supercomplexes * Antioxidant defense * SOD2
Obor OECD: Biochemistry and molecular biology
Impakt faktor: 6.020, rok: 2017

Mitochondrial electron transport chain (ETC) targeting shows a great promise in cancer therapy. It is particularly effective in tumors with high ETC activity where ETC-derived reactive oxygen species (ROS) are efficiently induced. Why modern ETC-targeted compounds are tolerated on the organismal level remains unclear. As most somatic cells are in non-proliferative state, the features associated with the ETC in quiescence could account for some of the specificity observed. Here we report that quiescent cells, despite increased utilization of the ETC and enhanced supercomplex assembly, are less susceptible to cell death induced by ETC disruption when glucose is not limiting. Mechanistically, this is mediated by the increased detoxification of ETC-derived ROS by mitochondrial antioxidant defense, principally by the superoxide dismutase 2 thioredoxin axis. In contrast, under conditions of glucose limitation, cell death is induced preferentially in quiescent cells and is correlated with intracellular ATP depletion but not with ROS. This is related to the inability of quiescent cells to compensate for the lost mitochondrial ATP production by the upregulation of glucose uptake. Hence, elevated ROS, not the loss of mitochondrially-generated ATP, are responsible for cell death induction by ETC disruption in ample nutrients condition, e.g. in well perfused healthy tissues, where antioxidant defense imparts specificity. However, in conditions of limited glucose, e.g. in poorly perfused tumors, ETC disruption causes rapid depletion of cellular ATP, optimizing impact towards tumor-associated dormant cells. In summary, we propose that antioxidant defense in quiescent cells is aided by local glucose limitations to ensure selectivity of ETC inhibition-induced cell death.
Trvalý link: http://hdl.handle.net/11104/0277051