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Expression of STING in Women with Morbid Obesity and Nonalcoholic Fatty Liver Disease

Authors :
Laia Bertran
Laia Adalid
Mercè Vilaró-Blay
Andrea Barrientos-Riosalido
Carmen Aguilar
Salomé Martínez
Fàtima Sabench
Daniel del Castillo
José Antonio Porras
Ajla Alibalic
Cristóbal Richart
Teresa Auguet
Source :
Metabolites, Vol 13, Iss 4, p 496 (2023)
Publication Year :
2023
Publisher :
MDPI AG, 2023.

Abstract

Nonalcoholic fatty liver disease (NAFLD) is the most prevalent chronic hepatic disease. Although mostly benign, this disease can evolve into nonalcoholic steatohepatitis (NASH). The stimulator of interferon genes (STING) plays an important role in the immune response against stressed cells, but this protein may also be involved in liver lipogenesis and microbiota composition. In this study, the role of STING in NAFLD was evaluated by RT–qPCR to analyze STING mRNA abundance and by immunohistochemical analysis to evaluate protein expression in liver biopsies from a cohort composed of 69 women with morbid obesity classified according to their liver involvement (normal liver, n = 27; simple steatosis (SS), n = 26; NASH, n = 16). The results showed that STING mRNA expression in the liver increases with the occurrence of NAFLD, specifically in the SS stage in which the degree of steatosis is mild or moderate. Protein analysis corroborated these results. Positive correlations were observed among hepatic STING mRNA abundance and gamma-glutamyl transferase and alkaline phosphatase levels, hepatic Toll-like receptor 9 expression and some circulating microbiota-derived bile acids. In conclusion, STING may be involved in the outcome and progression of NAFLD and may be related to hepatic lipid metabolism. However, further studies are needed to confirm these findings.

Details

Language :
English
ISSN :
22181989
Volume :
13
Issue :
4
Database :
Directory of Open Access Journals
Journal :
Metabolites
Publication Type :
Academic Journal
Accession number :
edsdoj.07d3fb6a59024e2cb7e70563b84ed45b
Document Type :
article
Full Text :
https://doi.org/10.3390/metabo13040496