Department of Physiology and Pathophysiology, Peking University Diabetes Center, Peking University Health Science Center, Beijing 100191, China.
Int J Endocrinol. 2010;2010:515136. doi: 10.1155/2010/515136. Epub 2010 Nov 14.
The dysfunction of pancreatic β-cell and the reduction in β-cell mass are the decisive events in the progression of type 2 diabetes. There is increasing evidence that cytokines play important roles in the procedure of β-cell failure. Cytokines, such as IL-1β, IFN-γ, TNF-α, leptin, resistin, adiponectin, and visfatin, have been shown to diversely regulate pancreatic β-cell function. Recently, islet-derived cytokine PANcreatic DERived factor (PANDER or FAM3B) has also been demonstrated to be a regulator of islet β-cell function. The change in cytokine profile in islet and plasma is associated with pancreatic β-cell dysfunction and apoptosis. In this paper, we summarize and discuss the recent studies on the effects of certain important cytokines on pancreatic β-cell function. The imbalance in deleterious and protective cytokines plays pivotal roles in the development and progression of pancreatic β-cell dysfunction under insulin-resistant conditions.
胰岛β细胞功能障碍和β细胞质量减少是 2 型糖尿病进展的决定性事件。越来越多的证据表明细胞因子在β细胞衰竭过程中发挥重要作用。细胞因子,如白细胞介素-1β、干扰素-γ、肿瘤坏死因子-α、瘦素、抵抗素、脂联素和内脂素,已被证明可多样化调节胰岛β细胞功能。最近,胰岛衍生细胞因子 PANcreatic DERived factor (PANDER 或 FAM3B) 也被证明是胰岛β细胞功能的调节剂。胰岛和血浆中细胞因子谱的变化与胰岛β细胞功能障碍和细胞凋亡有关。本文总结和讨论了某些重要细胞因子对胰岛β细胞功能的影响的最新研究。在胰岛素抵抗条件下,有害和保护性细胞因子的失衡在胰岛β细胞功能障碍的发生和发展中起着关键作用。