Abstract
Oxysterol sulfates are emerging as key players in lipid homeostasis, inflammation and immunity. Despite this, knowledge on their basal levels in fluids, cells and tissues and any changes associated with age, gender and diet in health and disease; as well as their spatio-temporal distribution in cell membranes and organelles have been greatly hampered by the lack of commercially available pure synthetic standards. Expansion of the panel of pure oxysterol sulfates standards is pivotal to improve our understanding on the impact of oxysterol sulfates at the membrane level and their role in cellular events. While the clinical significance, biophysical implications and biological relevance of oxysterol sulfates in fluids, cells and tissues remains largely unknown, knowledge already gathered on the precursors of oxysterol sulfates (e.g. oxysterols and cholesterol sulfate) can be used to guide researchers on the most relevant aspects to search for when screening for oxysterol sulfates bioavailability in (patho)physiological conditions which are crucial in the design of biophysical and of cell-based assays. Herein, we provide a review on the brief knowledge involving oxysterol sulfate and an overview on the biophysical implications and biological relevance of oxysterols and cholesterol sulfate useful to redirect further investigations on the role of oxysterol sulfates in health and disease.
| Original language | English |
|---|---|
| Pages (from-to) | 401-410 |
| Number of pages | 10 |
| Journal | Essays in Biochemistry |
| Volume | 68 |
| Issue number | 4 |
| Early online date | 28 Mar 2024 |
| DOIs | |
| Publication status | Published - 4 Dec 2024 |
Bibliographical note
Copyright © 2024 The Author(s). This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY: https://creativecommons.org/licenses/by/4.0/).Funding
A.R. acknowledges funding from FCT - Fundacao para a Ciencia e a Tecnologia, I.P., within Norma Transitoria - DL 57/2016/CP1346/CT0006. I.H.K.D. would like to acknowledge the funding support by Alzheimer’s Association [grant number AARGD-22-926459]. This publication is based upon work from COST Action 19105-Pan-European Network in Lipidomics and EpiLipidomics (EpiLipidNET) supported by COST (European Cooperation in Science and Technology). Open access for this article was enabled by the participation of Aston University in an all-inclusive Read & Publish agreement with Portland Press and the Biochemical Society under a transformative agreement with JISC.
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