Oxiapoptophagy: A type of cell death induced by some oxysterols.

Thomas Nury, Amira Zarrouk, Aline Yammine, John J Mackrill, Anne Vejux, Gérard Lizard

Journal: British journal of pharmacology 2021;178(16):3115-3123

PMID: 32579703

Abstract

Oxysterols are oxidized forms of cholesterol generated from cholesterol by auto-oxidation, enzymatic processes, or both. Some of them (7-ketocholesterol, 7β-hydroxycholesterol and 24(S)-hydroxycholesterol), when used at cytotoxic concentrations on different cell types from different species (mesenchymal bone marrow cells, monocytic cells and nerve cells), induce a type of cell death associated with OXIdative stress and several characteristics of APOPTOsis and autoPHAGY, defined as oxiapoptophagy. Oxidative stress is associated with overproduction of ROS, increased antioxidant enzyme activities, lipid peroxidation and protein carbonylation. Apoptosis is associated with activation of the mitochondrial pathway, opening of the mitochondrial permeability pore, loss of mitochondrial membrane potential, caspase-3 activation, PARP degradation, nuclear condensation and/or fragmentation. Autophagy is characterized by autophagic vacuoles revealed by monodansylcadaverine staining and transmission electron microscopy, plus increased ratio of LC-3II/LC-3I. In addition, morphological, topographical and functional changes of the peroxisome are observed. LINKED ARTICLES: This article is part of a themed issue on Oxysterols, Lifelong Health and Therapeutics. To view the other articles in this section visit http://onlinelibrary.wiley.com/doi/10.1111/bph.v178.16/issuetoc.

© 2020 The British Pharmacological Society.

Address: Team "Biochemistry of the Peroxisome, Inflammation and Lipid Metabolism" EA 7270/Inserm, University Bourgogne Franche-Comté, Dijon, France.; Faculty of Medicine, LR12ES05, Lab-NAFS "Nutrition - Functional Food & Vascular Health", University of Monastir, Monastir, Tunisia.; Laboratory of Biochemistry, Faculty of Medicine, University of Sousse, Sousse, Tunisia.; Team "Biochemistry of the Peroxisome, Inflammation and Lipid Metabolism" EA 7270/Inserm, University Bourgogne Franche-Comté, Dijon, France.; Bioactive Molecules Research Laboratory, Doctoral School of Sciences and Technologies, Faculty of Sciences, Lebanese University, Beirut, Lebanon.; Department of Physiology, School of Medicine, University College Cork, Cork, Ireland.

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