Tarlton Jamie M R, Patterson Steven, Graham Annette
Department of Biological and Biomedical Sciences, School of Health and Life Sciences, Glasgow Caledonian University, Glasgow G4 0BA, UK.
Biology (Basel). 2021 Jun 15;10(6):534. doi: 10.3390/biology10060534.
Alterations in lipid metabolism within beta cells and islets contributes to dysfunction and apoptosis of beta cells, leading to loss of insulin secretion and the onset of type 2 diabetes. Over the last decade, there has been an explosion of interest in understanding the landscape of gene expression which influences beta cell function, including the importance of small non-coding microRNA sequences in this context. This review sought to identify the microRNA sequences regulated by metabolic challenges in beta cells and islets, their targets, highlight their function and assess their possible relevance as biomarkers of disease progression in diabetic individuals. Predictive analysis was used to explore networks of genes targeted by these microRNA sequences, which may offer new therapeutic strategies to protect beta cell function and delay the onset of type 2 diabetes.
β细胞和胰岛内脂质代谢的改变会导致β细胞功能障碍和凋亡,进而导致胰岛素分泌丧失和2型糖尿病的发生。在过去十年中,人们对理解影响β细胞功能的基因表达格局产生了浓厚兴趣,其中包括小非编码微小RNA序列在这方面的重要性。本综述旨在确定β细胞和胰岛中受代谢挑战调控的微小RNA序列、它们的靶标,突出其功能,并评估它们作为糖尿病个体疾病进展生物标志物的潜在相关性。采用预测分析来探索这些微小RNA序列靶向的基因网络,这可能为保护β细胞功能和延缓2型糖尿病的发生提供新的治疗策略。