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

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 tri...

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Autores principales: López-Pastor, Andrea R., Infante-Menéndez, Jorge, González-Illanes, Tamara, González-López, Paula, González-Rodríguez, Águeda, García-Monzón, Carmelo, Vega de Céniga, Melina, Esparza, Leticia, Gómez-Hernández, Almudena, Escribano, Óscar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8713993/
https://www.ncbi.nlm.nih.gov/pubmed/34850865
http://dx.doi.org/10.1242/dmm.049173
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author López-Pastor, Andrea R.
Infante-Menéndez, Jorge
González-Illanes, Tamara
González-López, Paula
González-Rodríguez, Águeda
García-Monzón, Carmelo
Vega de Céniga, Melina
Esparza, Leticia
Gómez-Hernández, Almudena
Escribano, Óscar
author_facet López-Pastor, Andrea R.
Infante-Menéndez, Jorge
González-Illanes, Tamara
González-López, Paula
González-Rodríguez, Águeda
García-Monzón, Carmelo
Vega de Céniga, Melina
Esparza, Leticia
Gómez-Hernández, Almudena
Escribano, Óscar
author_sort López-Pastor, Andrea R.
collection PubMed
description 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.
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spelling pubmed-87139932021-12-29 Concerted regulation of non-alcoholic fatty liver disease progression by microRNAs in apolipoprotein E-deficient mice López-Pastor, Andrea R. Infante-Menéndez, Jorge González-Illanes, Tamara González-López, Paula González-Rodríguez, Águeda García-Monzón, Carmelo Vega de Céniga, Melina Esparza, Leticia Gómez-Hernández, Almudena Escribano, Óscar Dis Model Mech Research Article 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. The Company of Biologists Ltd 2021-12-24 /pmc/articles/PMC8713993/ /pubmed/34850865 http://dx.doi.org/10.1242/dmm.049173 Text en © 2021. Published by The Company of Biologists Ltd https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Article
López-Pastor, Andrea R.
Infante-Menéndez, Jorge
González-Illanes, Tamara
González-López, Paula
González-Rodríguez, Águeda
García-Monzón, Carmelo
Vega de Céniga, Melina
Esparza, Leticia
Gómez-Hernández, Almudena
Escribano, Óscar
Concerted regulation of non-alcoholic fatty liver disease progression by microRNAs in apolipoprotein E-deficient mice
title Concerted regulation of non-alcoholic fatty liver disease progression by microRNAs in apolipoprotein E-deficient mice
title_full Concerted regulation of non-alcoholic fatty liver disease progression by microRNAs in apolipoprotein E-deficient mice
title_fullStr Concerted regulation of non-alcoholic fatty liver disease progression by microRNAs in apolipoprotein E-deficient mice
title_full_unstemmed Concerted regulation of non-alcoholic fatty liver disease progression by microRNAs in apolipoprotein E-deficient mice
title_short Concerted regulation of non-alcoholic fatty liver disease progression by microRNAs in apolipoprotein E-deficient mice
title_sort concerted regulation of non-alcoholic fatty liver disease progression by micrornas in apolipoprotein e-deficient mice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8713993/
https://www.ncbi.nlm.nih.gov/pubmed/34850865
http://dx.doi.org/10.1242/dmm.049173
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