Concerted regulation of non-alcoholic fatty liver disease progression by microRNAs in apolipoprotein E-deficient mice

Author:

López-Pastor Andrea R.1,Infante-Menéndez Jorge1,González-Illanes Tamara1,González-López Paula1,González-Rodríguez Águeda23ORCID,García-Monzón Carmelo23ORCID,Vega de Céniga Melina45,Esparza Leticia45,Gómez-Hernández Almudena1ORCID,Escribano Óscar1ORCID

Affiliation:

1. Laboratory of Hepatic and Cardiovascular Diseases, Biochemistry and Molecular Biology Department, School of Pharmacy, Complutense University of Madrid, 28040 Madrid, Spain

2. Liver Research Unit, Hospital Universitario Santa Cristina, Instituto de Investigación Sanitaria Princesa, 28009 Madrid, Spain

3. CIBER of Hepatic and Digestive Diseases (CIBERehd), 28029 Madrid, Spain

4. Department of Angiology and Vascular Surgery, Hospital de Galdakao-Usansolo, Galdakao, 48960 Bizkaia, Spain

5. Biocruces Bizkaia Health Research Institute, Barakaldo, 48903 Bizkaia, Spain

Abstract

ABSTRACT The prevalence of non-alcoholic fatty liver disease (NAFLD) is constantly increasing, and altered expression of microRNAs (miRNAs) fosters the development and progression of many pathologies, including NAFLD. Therefore, we explored the role of new miRNAs involved in the molecular mechanisms that trigger NAFLD progression and evaluated them as biomarkers for diagnosis. As a NAFLD model, we used apolipoprotein E-deficient mice administered a high-fat diet for 8 or 18 weeks. We demonstrated that insulin resistance and decreased lipogenesis and autophagy observed after 18 weeks on the diet are related to a concerted regulation carried out by miR-26b-5p, miR-34a-5p, miR-149-5p and miR-375-3p. We also propose circulating let-7d-5p and miR-146b-5p as potential biomarkers of early stages of NAFLD. Finally, we confirmed that circulating miR-34a-5p and miR-375-3p are elevated in the late stages of NAFLD and that miR-27b-3p and miR-122-5p are increased with disease progression. Our results reveal a synergistic regulation of key processes in NAFLD development and progression by miRNAs. Further investigation is needed to unravel the roles of these miRNAs for developing new strategies for NAFLD treatment. This article has an associated First Person interview with the joint first authors of the paper.

Funder

Ministerio de Ciencia, Innovación y Universidades

Universidad Complutense de Madrid

Comunidad de Madrid

European Social Fund

Publisher

The Company of Biologists

Subject

General Biochemistry, Genetics and Molecular Biology,Immunology and Microbiology (miscellaneous),Medicine (miscellaneous),Neuroscience (miscellaneous)

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