Schönecker S, Kraushaar U, Guenther E, Gerst F, Ullrich S, Häring H-U, Königsrainer A, Barthlen W, Drews G, Krippeit-Drews P
Department of Electrophysiology, NMI Natural and Medical Sciences Institute at the University of Tübingen, Reutlingen.
Division of Endocrinology, Department of Internal Medicine and IDM, Diabetology, Vascular Medicine, Nephrology, and Clinical Chemistry, University of Tübingen.
Exp Clin Endocrinol Diabetes. 2015 May;123(5):296-8. doi: 10.1055/s-0035-1547217. Epub 2015 Apr 8.
This study demonstrates for the first time that the microelectrode array (MEA) technique allows analysis of electrical activity of islets isolated from human biopsies. We have shown before that this method, i.e., measuring beta cell electrical activity with extracellular electrodes, is a powerful tool to assess glucose responsiveness of isolated murine islets. In the present study, human islets were shown to exhibit glucose-dependent oscillatory electrical activity. The glucose responsiveness could be furthermore demonstrated by an increase of insulin secretion in response to glucose. Electrical activity was increased by tolbutamide and inhibited by diazoxide. In human islets bursts of electrical activity were markedly blunted by the Na(+) channel inhibitor tetrodotoxin which does not affect electrical activity in mouse islets. Thus, the MEA technique emerges as a powerful tool to decipher online the unique features of human islets.Additionally, this technique will enable research with human islets even if only a few islets are available and it will allow a fast and easy test of metabolic integrity of islets destined for transplantation.
本研究首次证明,微电极阵列(MEA)技术能够分析从人类活检组织中分离出的胰岛的电活动。我们之前已经表明,这种方法,即使用细胞外电极测量β细胞电活动,是评估分离的小鼠胰岛葡萄糖反应性的有力工具。在本研究中,人类胰岛表现出葡萄糖依赖性振荡电活动。此外,葡萄糖反应性可通过葡萄糖刺激后胰岛素分泌增加来证明。甲苯磺丁脲可增加电活动,而二氮嗪则抑制电活动。在人类胰岛中,电活动的爆发被钠通道抑制剂河豚毒素显著减弱,而河豚毒素并不影响小鼠胰岛的电活动。因此,MEA技术成为解读人类胰岛独特特征的有力工具。此外,即使只有少数胰岛可用,该技术也能用于人类胰岛研究,并且它将允许对用于移植的胰岛的代谢完整性进行快速简便的测试。