Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.
Diabetes Obes Metab. 2013 Sep;15 Suppl 3:130-6. doi: 10.1111/dom.12152.
β-Cell failure is crucial for the onset and progression of human type 2 diabetes, and a few studies have suggested that inflammation may play a role. Immune cell infiltration has been reported in subpopulations of islets in some cases of human type 2 diabetes, and altered gene expression of a few cytokines and chemokines has been observed in isolated islets and laser captured β-cells from diabetic subjects. Recent observations on the links between inflammation, apoptosis and autophagy are putting the focus on the possibility that modulating the autophagic processes could protect the β-cells from cytotoxicity induced by inflammatory mediators.
β 细胞衰竭是人类 2 型糖尿病发病和进展的关键,有几项研究表明炎症可能起作用。在某些人类 2 型糖尿病病例中,已经报道了胰岛亚群中的免疫细胞浸润,并且在分离的胰岛和激光捕获的糖尿病患者的 β 细胞中观察到少数细胞因子和趋化因子的基因表达改变。最近关于炎症、细胞凋亡和自噬之间联系的观察结果使人们关注到调节自噬过程可能保护 β 细胞免受炎症介质诱导的细胞毒性的可能性。