Zhang Xiao-Xi, Pan Yan-Hong, Huang Yan-Mei, Zhao Hai-Lu
Xiao-Xi Zhang, Yan-Hong Pan, Yan-Mei Huang, Hai-Lu Zhao, Centre of Diabetic Systems Medicine, Guangxi Key Laboratory of Excellence, Guilin Medical University, Guilin 541004, Guangxi Zhuang Autonomous Region, China.
World J Diabetes. 2016 May 10;7(9):189-97. doi: 10.4239/wjd.v7.i9.189.
The neuroendocrine hormone amylin, also known as islet amyloid polypeptide, is co-localized, co-packaged and co-secreted with insulin from adult pancreatic islet β cells to maintain glucose homeostasis. Specifically, amylin reduces secretion of nutrient-stimulated glucagon, regulates blood pressure with an effect on renin-angiotensin system, and delays gastric emptying. The physiological actions of human amylin attribute to the conformational α-helix monomers whereas the misfolding instable oligomers may be detrimental to the islet β cells and further transform to β-sheet fibrils as amyloid deposits. No direct evidence proves that the amylin fibrils in amyloid deposits cause diabetes. Here we also have performed a systematic review of human amylin gene changes and reported the S20G mutation is minor in the development of diabetes. In addition to the metabolic effects, human amylin may modulate autoimmunity and innate inflammation through regulatory T cells to impact on both human type 1 and type 2 diabetes.
神经内分泌激素胰淀素,也称为胰岛淀粉样多肽,与胰岛素共同定位、共同包装并从成年胰腺胰岛β细胞共同分泌,以维持葡萄糖稳态。具体而言,胰淀素可减少营养刺激的胰高血糖素分泌,通过对肾素-血管紧张素系统的作用调节血压,并延迟胃排空。人胰淀素的生理作用归因于构象α-螺旋单体,而错误折叠的不稳定寡聚体可能对胰岛β细胞有害,并进一步转化为β-折叠原纤维形成淀粉样沉积物。没有直接证据证明淀粉样沉积物中的胰淀素纤维会导致糖尿病。在这里,我们还对人胰淀素基因变化进行了系统综述,并报告S20G突变在糖尿病发展中作用较小。除代谢作用外,人胰淀素可能通过调节性T细胞调节自身免疫和先天性炎症,从而影响人类1型和2型糖尿病。