Sou Yong Ling, Chilian William M, Ratnam Wickneswari, Zain Shamsul Mohd, Syed Abdul Kadir Sharifah Zamiah, Pan Yan, Pung Yuh-Fen
Division of Biomedical Science, Faculty of Science and Engineering, University of Nottingham Malaysia, Semenyih, Selangor 43500, Malaysia.
Department of Integrative Medical Sciences, Northeast Ohio Medical University, Rootstown, OH 44272, USA.
Precis Clin Med. 2024 Sep 20;7(3):pbae021. doi: 10.1093/pcmedi/pbae021. eCollection 2024 Sep.
Type 2 diabetes mellitus (T2DM) is a metabolic disease that is characterized by chronic hyperglycaemia. MicroRNAs (miRNAs) are single-stranded, small non-coding RNAs that play important roles in post-transcriptional gene regulation. They are negative regulators of their target messenger RNAs (mRNAs), in which they bind either to inhibit mRNA translation, or to induce mRNA decay. Similar to proteins, miRNAs exist in different isoforms (isomiRs). miRNAs and isomiRs are selectively loaded into small extracellular vesicles, such as the exosomes, to protect them from RNase degradation. In T2DM, exosomal miRNAs produced by different cell types are transported among the primary sites of insulin action. These interorgan crosstalk regulate various T2DM-associated pathways such as adipocyte inflammation, insulin signalling, and β cells dysfunction among many others. In this review, we first focus on the mechanism of exosome biogenesis, followed by miRNA biogenesis and isomiR formation. Next, we discuss the roles of exosomal miRNAs and isomiRs in the development of T2DM and provide evidence from clinical studies to support their potential roles as T2DM biomarkers. Lastly, we highlight the use of exosomal miRNAs and isomiRs in personalized medicine, as well as addressing the current challenges and future opportunities in this field. This review summarizes how research on exosomal miRNAs and isomiRs has developed from the very basic to clinical applications, with the goal of advancing towards the era of personalized medicine.
2型糖尿病(T2DM)是一种以慢性高血糖为特征的代谢性疾病。微小RNA(miRNA)是单链小非编码RNA,在转录后基因调控中发挥重要作用。它们是其靶信使RNA(mRNA)的负调节因子,通过与之结合来抑制mRNA翻译或诱导mRNA降解。与蛋白质类似,miRNA也存在不同的异构体(isomiR)。miRNA和isomiR被选择性地装载到小细胞外囊泡中,如外泌体,以保护它们免受核糖核酸酶降解。在T2DM中,不同细胞类型产生的外泌体miRNA在胰岛素作用的主要部位之间运输。这些器官间的相互作用调节多种与T2DM相关的途径,如脂肪细胞炎症、胰岛素信号传导以及β细胞功能障碍等。在本综述中,我们首先关注外泌体生物发生机制,接着是miRNA生物发生和isomiR形成。接下来,我们讨论外泌体miRNA和isomiR在T2DM发展中的作用,并提供临床研究证据以支持它们作为T2DM生物标志物的潜在作用。最后,我们强调外泌体miRNA和isomiR在个性化医疗中的应用,以及探讨该领域当前的挑战和未来机遇。本综述总结了外泌体miRNA和isomiR的研究如何从基础研究发展到临床应用,目标是迈向个性化医疗时代。