miRNA-642a-3p protects β cells from glucolipotoxicity.

IF 6.1 2区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
Molecular Therapy. Nucleic Acids Pub Date : 2025-03-25 eCollection Date: 2025-06-10 DOI:10.1016/j.omtn.2025.102498
Sandra Sofia Pinhanços, João Teixeira de Oliveira, C Henrique Alves, Cláudia M Deus, Twan J J de Winter, Sofia Viana, Flávio Reis, Jorge Santos, Mijke Buitinga, Françoise Carlotti, Lino Ferreira, Martin Gotthardt, John Jones, Hugo Fernandes
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引用次数: 0

Abstract

The incidence of type 2 diabetes mellitus (T2DM) is tightly linked to obesity. High levels of circulating glucose and saturated free fatty acids (FFAs), known as glucolipotoxicity (GLT), is implicated in β cell dysfunction and/or death. This study aims to identify miRNAs capable of protecting β cells from GLT-induced cell death (GICD). A library of 2,080 human miRNA mimics was transfected in β cells followed by exposure to GLT. We identified 45 miRNAs capable of protecting β cells from GICD and selected miR-642a-3p for further studies. RNA-seq revealed that miR-642a-3p restored the expression of β cell identity genes and modulated pathways associated with cell survival and lipid metabolism. Moreover, we showed that transfection of β cells with miR-642a-3p protected them from GLT-induced changes in insulin secretion. Compared with the control, hypercaloric-fed mice showed a trend toward decreased expression of GLT-protective miRNAs. Notably, we demonstrated that miR-642a-3p expression was downregulated in human islets isolated from T2DM patients compared with non-diabetic controls. Importantly, in obese patients, the expression of GLT-protective miRNAs in plasma-derived extracellular vesicles was increased in non-diabetic patients. Overall, we have identified a potential dual role for miR-642a-3p as both a biomarker and a facilitator of β cell survival and function, offering a novel theranostic tool for the management of diabetes and/or obesity.

miRNA-642a-3p保护β细胞免受糖脂毒性。
2型糖尿病(T2DM)的发病率与肥胖密切相关。高水平的循环葡萄糖和饱和游离脂肪酸(FFAs),被称为糖脂毒性(GLT),与β细胞功能障碍和/或死亡有关。本研究旨在鉴定能够保护β细胞免受glt诱导的细胞死亡(GICD)的mirna。将2,080个人类miRNA模拟物库转染β细胞,然后暴露于GLT。我们鉴定了45种能够保护β细胞免受GICD的mirna,并选择了miR-642a-3p进行进一步研究。RNA-seq显示,miR-642a-3p恢复了β细胞身份基因的表达,并调节了与细胞存活和脂质代谢相关的途径。此外,我们发现转染miR-642a-3p可以保护β细胞免受glt诱导的胰岛素分泌变化。与对照组相比,高热量喂养小鼠glt保护性mirna的表达有降低的趋势。值得注意的是,我们证明了与非糖尿病对照组相比,从T2DM患者分离的人胰岛中miR-642a-3p的表达下调。重要的是,在肥胖患者中,非糖尿病患者血浆来源的细胞外囊泡中glt保护性mirna的表达增加。总的来说,我们已经确定了miR-642a-3p作为β细胞存活和功能的生物标志物和促进剂的潜在双重作用,为糖尿病和/或肥胖的治疗提供了一种新的治疗工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Molecular Therapy. Nucleic Acids
Molecular Therapy. Nucleic Acids MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
15.40
自引率
1.10%
发文量
336
审稿时长
20 weeks
期刊介绍: Molecular Therapy Nucleic Acids is an international, open-access journal that publishes high-quality research in nucleic-acid-based therapeutics to treat and correct genetic and acquired diseases. It is the official journal of the American Society of Gene & Cell Therapy and is built upon the success of Molecular Therapy. The journal focuses on gene- and oligonucleotide-based therapies and publishes peer-reviewed research, reviews, and commentaries. Its impact factor for 2022 is 8.8. The subject areas covered include the development of therapeutics based on nucleic acids and their derivatives, vector development for RNA-based therapeutics delivery, utilization of gene-modifying agents like Zn finger nucleases and triplex-forming oligonucleotides, pre-clinical target validation, safety and efficacy studies, and clinical trials.
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