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Lookup NU author(s): Dr Jack LeslieORCiD, Professor Fiona OakleyORCiD
This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (CC BY-NC-ND).
ObjectiveNon-alcoholic fatty liver disease (NAFLD) is a silent pandemic associated with obesity and the Metabolic Syndrome, linked to increased cardiovascular- and cirrhosis-related morbidity and mortality. A complete understanding of the adaptive compensatory metabolic programs that modulate non-alcoholic steatohepatitis (NASH) progression is missing.Methods and ResultsTranscriptomics analysis of liver biopsies in patients with NASH revealed that NASH progression is associated with rewiring of metabolic pathways, including upregulation of the de novo lipid/cholesterol synthesis and fatty acid remodelling. The modulation of these metabolic programs was achieved through the activation of Sterol Regulatory Element-Binding Proteins (SREBPs) transcriptional networks; however, it is still debated whether, in the context of NASH, activation of SREBPs acts as a pathogenic driver of lipotoxicity, or promotes the biosynthesis of protective lipids that buffer excessive lipid accumulation, preventing inflammation and fibrosis. To elucidate the pathophysiological role of SCAP/SREBP’s in NASH and wound-healing response, we used an Insig1 deficient hyper-efficient SREBP activator murine model. Despite enhanced lipid and cholesterol biosynthesis the Insig1 KO mice had similar systemic metabolism and insulin sensitivity to Het/WT littermates. Moreover, the activation of SREBPs resulted in the remodelling of the lipidome, decreased hepatocellular damage, and improved wound-healing responses.ConclusionOur study provides actionable knowledge about the pathways and mechanisms involved in NAFLD pathogenesis, which may prove useful for the development of new therapeutic strategies. Moreover, our results suggest that the SCAP/SREBP/INSIG1 trio governs transcriptional programs aimed at protecting the liver from lipotoxic insults in NASH.Non-alcoholic fatty liver disease (NAFLD)de novolipogenesis (DNL)lipid remodellingwestern dietcarbon tetracholride (CCl4)liver regeneration
Author(s): Azzu V, Vacca M, Kamzolas I, Hall Z, Leslie J, Carobbio S, Virtue S, Davies SE, Lukasik A, Dale M, Bohooly-Y M, Acharjee A, Linden D, Bidualt G, Petsalaki E, Griffin Jl, Oakley F, Allison ME, Vidal-Puig A
Publication type: Article
Publication status: Published
Journal: Molecular Metabolism
Year: 2021
Volume: 48
Print publication date: 01/06/2021
Online publication date: 17/03/2021
Acceptance date: 06/03/2021
Date deposited: 09/11/2023
ISSN (electronic): 2212-8778
Publisher: Elsevier BV
URL: https://doi.org/10.1016/j.molmet.2021.101210
DOI: 10.1016/j.molmet.2021.101210
Data Access Statement: All of the raw data (FASTQ files) and relevant metadata are available in the Array Express database (www.ebi.ac.uk/arrayexpress) under accession numbers E-MTAB-9815 and E-MTAB-9864.
PubMed id: 33722690
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