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

被引:11
作者
Lopez-Pastor, Andrea R. [1 ]
Infante-Menendez, Jorge [1 ]
Gonzalez-Illanes, Tamara [1 ]
Gonzalez-Lopez, Paula [1 ]
Gonzalez-Rodriguez, Agueda [2 ,3 ]
Garcia-Monzon, Carmelo [2 ,3 ]
Vega de Ceniga, Melina [4 ,5 ]
Esparza, Leticia [4 ,5 ]
Gomez-Hernandez, Almudena [1 ]
Escribano, Oscar [1 ]
机构
[1] Univ Complutense Madrid, Sch Pharm, Biochem & Mol Biol Dept, Lab Hepat & Cardiovasc Dis, Madrid 28040, Spain
[2] Hosp Univ Santa Cristina, Inst Invest Sanitaria Princesa, Liver Res Unit, Madrid 28009, Spain
[3] CIBER Hepat & Digest Dis CIBERehd, Madrid 28029, Spain
[4] Hosp Galdakao Usansolo, Dept Angiol & Vasc Surg, Bizkaia 48960, Spain
[5] Biocruces Bizkaia Hlth Res Inst, Bizkaia 48903, Spain
关键词
Non-alcoholic fatty liver disease; MicroRNAs; Lipid metabolism; Insulin resistance; Autophagy; Extracellular vesicles; INSULIN-RESISTANCE; HEPATIC STEATOSIS; MESSENGER-RNA; STEATOHEPATITIS; MECHANISMS; RECEPTOR; OBESITY; SIRT1; HEPATOCYTES; EXPRESSION;
D O I
10.1242/dmm.049173
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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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页数:15
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