Oxysterols are potential physiological regulators of ageing.

Philippe de Medina, Sandrine Silvente-Poirot, Marc Poirot

Journal: Ageing research reviews 2022;77():101615

PMID: 35351610

Abstract

Delaying and even reversing ageing is a major public health challenge with a tremendous potential to postpone a plethora of diseases including cancer, metabolic syndromes and neurodegenerative disorders. A better understanding of ageing as well as the development of innovative anti-ageing strategies are therefore an increasingly important field of research. Several biological processes including inflammation, proteostasis, epigenetic, oxidative stress, stem cell exhaustion, senescence and stress adaptive response have been reported for their key role in ageing. In this review, we describe the relationships that have been established between cholesterol homeostasis, in particular at the level of oxysterols, and ageing. Initially considered as harmful pro-inflammatory and cytotoxic metabolites, oxysterols are currently emerging as an expanding family of fine regulators of various biological processes involved in ageing. Indeed, depending of their chemical structure and their concentration, oxysterols exhibit deleterious or beneficial effects on inflammation, oxidative stress and cell survival. In addition, stem cell differentiation, epigenetics, cellular senescence and proteostasis are also modulated by oxysterols. Altogether, these data support the fact that ageing is influenced by an oxysterol profile. Further studies are thus required to explore more deeply the impact of the "oxysterome" on ageing and therefore this cholesterol metabolic pathway constitutes a promising target for future anti-ageing interventions.

Copyright © 2022 Elsevier B.V. All rights reserved.

Address: Team INOV, Cancer Research Center of Toulouse, UMR 1037 Inserm, UMR 5071 CNRS, University of Toulouse 3, Toulouse, France. Electronic address: [email protected].; Team INOV, Cancer Research Center of Toulouse, UMR 1037 Inserm, UMR 5071 CNRS, University of Toulouse 3, Toulouse, France.; Team INOV, Cancer Research Center of Toulouse, UMR 1037 Inserm, UMR 5071 CNRS, University of Toulouse 3, Toulouse, France. Electronic address: [email protected].
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