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载脂蛋白 E 缺陷型小鼠中 microRNAs 对非酒精性脂肪性肝病进展的协同调控。

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

机构信息

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

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

出版信息

Dis Model Mech. 2021 Dec 1;14(12). doi: 10.1242/dmm.049173. Epub 2021 Dec 24.

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.

摘要

非酒精性脂肪性肝病(NAFLD)的患病率不断上升,而 microRNAs(miRNAs)的表达改变促进了许多病理学的发展和进展,包括 NAFLD。因此,我们探讨了参与触发 NAFLD 进展的分子机制的新 miRNAs 的作用,并将其评估为诊断的生物标志物。作为 NAFLD 模型,我们使用载脂蛋白 E 缺陷小鼠给予高脂肪饮食 8 或 18 周。我们证明,饮食 18 周后观察到的胰岛素抵抗和脂肪生成减少以及自噬减少与 miR-26b-5p、miR-34a-5p、miR-149-5p 和 miR-375-3p 的协同调节有关。我们还提出循环 let-7d-5p 和 miR-146b-5p 作为 NAFLD 早期阶段的潜在生物标志物。最后,我们证实循环 miR-34a-5p 和 miR-375-3p 在 NAFLD 的晚期阶段升高,而 miR-27b-3p 和 miR-122-5p 在疾病进展时增加。我们的结果揭示了 miRNAs 对 NAFLD 发展和进展中关键过程的协同调节。需要进一步研究来阐明这些 miRNAs 在开发 NAFLD 治疗新策略中的作用。本文有一篇与论文共同第一作者的相关第一人称采访。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66dd/8713993/19cf2c8b175c/dmm-14-049173-g1.jpg

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