Department of Cell and Development Biology, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Charles Perkins Centre, Faculty of Medicine and Health, University of Sydney, Camperdown, NSW, Australia.
Front Endocrinol (Lausanne). 2021 Apr 26;12:667170. doi: 10.3389/fendo.2021.667170. eCollection 2021.
Insulin-producing β-cells constitute the majority of the cells in the pancreatic islets. Dysfunction of these cells is a key factor in the loss of glucose regulation that characterizes type 2 diabetes. The regulation of many of the functions of β-cells relies on their close interaction with the intra-islet microvasculature, comprised of endothelial cells and pericytes. In addition to providing islet blood supply, cells of the islet vasculature directly regulate β-cell activity through the secretion of growth factors and other molecules. These factors come from capillary mural pericytes and endothelial cells, and have been shown to promote insulin gene expression, insulin secretion, and β-cell proliferation. This review focuses on the intimate crosstalk of the vascular cells and β-cells and its role in glucose homeostasis and diabetes.
产生胰岛素的β细胞构成了胰岛中大多数的细胞。这些细胞的功能障碍是 2 型糖尿病特征性葡萄糖调节丧失的关键因素。β细胞的许多功能的调节依赖于它们与胰岛内微血管的紧密相互作用,这些微血管由内皮细胞和周细胞组成。除了提供胰岛的血液供应外,胰岛血管系统的细胞还通过分泌生长因子和其他分子直接调节β细胞的活性。这些因子来自毛细血管壁周细胞和内皮细胞,并已被证明可促进胰岛素基因表达、胰岛素分泌和β细胞增殖。这篇综述主要关注血管细胞和β细胞之间的密切相互作用及其在葡萄糖稳态和糖尿病中的作用。