Mitochondrial respiration supports autophagy to provide stress resistance during quiescence
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Blecha, Jan
Naraine, Ravindra
Mikesova, Jana
Abaffy, Pavel
Pecinova, Alena
Milosevic, Mirko
Bohuslavova, Romana
Prochazka, Jan
Khan, Shawez
Novotna, Eliska
Sindelka, Radek
Machan, Radek
Dewerchin, Mieke
Neuzil, Jiri
et al.
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Abstract
Mitochondrial oxidative phosphorylation (OXPHOS) generates ATP, but OXPHOS also supports biosynthesis during proliferation. In contrast, the role of OXPHOS during quiescence, beyond ATP production, is not well understood. Using mouse models of inducible OXPHOS deficiency in all cell types or specifically in the vascular endothelium that negligibly relies on OXPHOS-derived ATP, we show that selectively during quiescence OXPHOS provides oxidative stress resistance by supporting macroautophagy/autophagy. Mechanistically, OXPHOS constitutively generates low levels of endogenous ROS that induce autophagy via attenuation of ATG4B activity, which provides protection from ROS insult. Physiologically, the OXPHOS-autophagy system (i) protects healthy tissue from toxicity of ROS-based anticancer therapy, and (ii) provides ROS resistance in the endothelium, ameliorating systemic LPS-induced inflammation as well as inflammatory bowel disease. Hence, cells acquired mitochondria during evolution to profit from oxidative metabolism, but also built in an autophagy-based ROS-induced protective mechanism to guard against oxidative stress associated with OXPHOS function during quiescence. Abbreviations: AMPK: AMP-activated protein kinase; AOX: alternative oxidase; Baf A: bafilomycin A1; CI, respiratory complexes I; DCF-DA: 2′,7′-dichlordihydrofluorescein diacetate; DHE: dihydroethidium; DSS: dextran sodium sulfate; ΔΨmi: mitochondrial inner membrane potential; EdU: 5-ethynyl-2’-deoxyuridine; ETC: electron transport chain; FA: formaldehyde; HUVEC; human umbilical cord endothelial cells; IBD: inflammatory bowel disease; LC3B: microtubule associated protein 1 light chain 3 beta; LPS: lipopolysaccharide; MEFs: mouse embryonic fibroblasts; MTORC1: mechanistic target of rapamycin kinase complex 1; mtDNA: mitochondrial DNA; NAC: N-acetyl cysteine; OXPHOS: oxidative phosphorylation; PCs: proliferating cells; PE: phosphatidylethanolamine; PEITC: phenethyl isothiocyanate; QCs: quiescent cells; ROS: reactive oxygen species; PLA2: phospholipase A2, WB: western blot.
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Autophagy
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© 2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way.
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Biochemistry and cell biology
Science & Technology
Life Sciences & Biomedicine
Cell Biology
ATG4B
biosynthesis
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Magalhaes-Novais, S; Blecha, J; Naraine, R; Mikesova, J; Abaffy, P; Pecinova, A; Milosevic, M; Bohuslavova, R; Prochazka, J; Khan, S; Novotna, E; Sindelka, R; Machan, R; Dewerchin, M; Vlcak, E; Kalucka, J; Stemberkova Hubackova, S; Benda, A; Goveia, J; Mracek, T; Barinka, C; Carmeliet, P; Neuzil, J; Rohlenova, K; Rohlena, J, Mitochondrial respiration supports autophagy to provide stress resistance during quiescence, Autophagy, 2022