Xu Fei, Liu Jing, Na Lixin, Chen Linjun
Department of Microbiology and Immunology, Shanghai University of Medicine & Health Sciences, Shanghai, China.
Collaborative Innovation Center of Shanghai University of Medicine & Health Sciences, Shanghai, China.
Front Cell Dev Biol. 2020 Aug 28;8:748. doi: 10.3389/fcell.2020.00748. eCollection 2020.
Diabetes, a metabolic disease with multiple causes characterized by high blood sugar, has become a public health problem. Hyperglycaemia is caused by deficiencies in insulin secretion, impairment of insulin function, or both. The insulin secreted by pancreatic β cells is the only hormone in the body that lowers blood glucose levels and plays vital roles in maintaining glucose homeostasis. Therefore, investigation of the molecular mechanisms of pancreatic β cell differentiation and function is necessary to elucidate the processes involved in the onset of diabetes. Although numerous studies have shown that transcriptional regulation is essential for the differentiation and function of pancreatic β cells, increasing evidence indicates that epigenetic mechanisms participate in controlling the fate and regulation of these cells. Epigenetics involves heritable alterations in gene expression caused by DNA methylation, histone modification and non-coding RNA activity that does not result in DNA nucleotide sequence alterations. Recent research has revealed that a variety of epigenetic modifications play an important role in the development of diabetes. Here, we review the mechanisms by which epigenetic regulation affects β cell differentiation and function.
糖尿病是一种由多种原因引起的以高血糖为特征的代谢性疾病,已成为一个公共卫生问题。高血糖症是由胰岛素分泌不足、胰岛素功能受损或两者兼而有之引起的。胰腺β细胞分泌的胰岛素是体内唯一能降低血糖水平并在维持葡萄糖稳态中起重要作用的激素。因此,研究胰腺β细胞分化和功能的分子机制对于阐明糖尿病发病过程是必要的。尽管大量研究表明转录调控对于胰腺β细胞的分化和功能至关重要,但越来越多的证据表明表观遗传机制参与控制这些细胞的命运和调控。表观遗传学涉及由DNA甲基化、组蛋白修饰和非编码RNA活性引起的基因表达的可遗传改变,而这些改变不会导致DNA核苷酸序列的改变。最近的研究表明,多种表观遗传修饰在糖尿病的发生发展中起重要作用。在此,我们综述表观遗传调控影响β细胞分化和功能的机制。