Department of Chemistry and Molecular Biology, University of Gothenburg, Kemivägen 10, 41296, Gothenburg, Sweden.
Department of Physiology, Sahlgrenska Academy, University of Gothenburg, Medicinaregatan 11-13, 41390, Gothenburg, Sweden.
Angew Chem Int Ed Engl. 2021 Mar 29;60(14):7593-7596. doi: 10.1002/anie.202015902. Epub 2021 Feb 26.
Recent work has shown that chemical release during the fundamental cellular process of exocytosis in model cell lines is not all-or-none. We tested this theory for vesicular release from single pancreatic beta cells. The vesicles in these cells release insulin, but also serotonin, which is detectible with amperometric methods. Traditionally, it is assumed that exocytosis in beta cells is all-or-none. Here, we use a multidisciplinary approach involving nanoscale amperometric chemical methods to explore the chemical nature of insulin exocytosis. We amperometrically quantified the number of serotonin molecules stored inside of individual nanoscale vesicles (39 317±1611) in the cell cytoplasm before exocytosis and the number of serotonin molecules released from single cells (13 310±1127) for each stimulated exocytosis event. Thus, beta cells release only one-third of their granule content, clearly supporting partial release in this system. We discuss these observations in the context of type-2 diabetes.
最近的研究表明,在模型细胞系中胞吐这一基本细胞过程中,化学物质的释放并非全有或全无。我们针对从单个胰腺β细胞中囊泡释放来验证这一理论。这些细胞中的囊泡释放胰岛素,但也释放血清素,后者可以通过安培法检测到。传统上,人们认为β细胞中的胞吐作用是全有或全无的。在这里,我们使用涉及纳米安培化学方法的多学科方法来探索胰岛素胞吐的化学性质。我们通过安培法在胞吐作用之前量化了单个纳米囊泡(39317±1611 个)内储存的血清素分子数量,以及每个刺激胞吐作用事件中从单个细胞释放的血清素分子数量(13310±1127 个)。因此,β细胞仅释放其颗粒内容物的三分之一,这清楚地支持了该系统中的部分释放。我们在 2 型糖尿病的背景下讨论了这些观察结果。