Department of Medicine, University of Toronto, Toronto, ON, Canada.
Diabetologia. 2012 Apr;55(4):877-80. doi: 10.1007/s00125-012-2483-7. Epub 2012 Feb 4.
According to our current understanding of insulin exocytosis, insulin granules dock on the plasma membrane, undergo priming and then wait for calcium-triggered fusion. In this issue of Diabetologia, Hoppa et al (doi 10.1007/s00125-011-2400-5 ) report that cholinergic stimulation induces granule-granule, or multivesicular, fusion to effect more efficient insulin release. Other exocytotic modes of insulin secretion, particularly those induced by incretin stimulation, include orderly granule fusion with granules already fused with the plasma membrane, called sequential exocytosis, and recruitment of newcomer granules to fuse with plasma membrane with minimal time for docking and priming. The molecular machineries that mediate these distinct exocytotic modes of granule-granule fusion and newcomer granules remain undefined, but they could be therapeutically targeted to couple to cholinergic and incretin stimulation to rescue the deficient glucose-stimulated insulin secretion in diabetes.
根据我们目前对胰岛素胞吐作用的理解,胰岛素颗粒在与质膜融合之前,先停靠在质膜上,然后进行“引发”,再等待钙离子触发融合。在本期《糖尿病学》杂志中,Hoppa 等人(doi:10.1007/s00125-011-2400-5)报告称,胆碱能刺激诱导颗粒-颗粒或多泡体融合,从而更有效地释放胰岛素。胰岛素分泌的其他胞吐作用模式,特别是由肠促胰岛素刺激引起的模式,包括有序的颗粒融合与已经与质膜融合的颗粒,称为顺序胞吐作用,以及新颗粒的募集与质膜融合,在停靠和引发方面的时间最短。介导这些不同的颗粒-颗粒融合和新颗粒胞吐作用模式的分子机制尚不清楚,但可以作为治疗靶点,与胆碱能和肠促胰岛素刺激相偶联,以挽救糖尿病中葡萄糖刺激的胰岛素分泌不足。