小岛
微流控
电生理学
联轴节(管道)
葡萄糖稳态
细胞培养
生物
细胞生物学
生物物理学
化学
胰岛素
纳米技术
内分泌学
材料科学
神经科学
医学
内科学
遗传学
冶金
胰岛素抵抗
作者
Marie Lallouet,Loïc Olçomendy,Julien Gaitan,Killian Montiège,Marie Monchablon,Antoine Pirog,Dorian Chapeau,Emilie Puginier,Sylvie Renaud,Matthieu Raoux,Jochen Lang
出处
期刊:Lab on a Chip
[Royal Society of Chemistry]
日期:2025-01-01
卷期号:25 (7): 1831-1841
被引量:3
摘要
Pancreatic islets play a major role in glucose homeostasis as well as in diabetes, and islets-on-chip devices have been mainly developed using optical means for on-line monitoring. In contrast, no well-characterized electrophysiological platform for on-line analysis with unrivalled temporal resolution has been reported. Extracellular electrophysiology monitors two crucial parameters, islet β-cell activity and β-to-β-cell coupling, does not require chemical or genetic probes with inherent potential bias, is non-invasive and permits repetitive long-term monitoring. We have now developed and characterized a microfluidic islets-on-chip for combined electrophysiology (on-line) and hormone monitoring (off-line) with two chambers for concomitant monitoring. Fabrication of the device, based on commercial or easily manufacturable components, is within the reach of non-specialized laboratories. The chip permits convenient loading as well as long-term culture with comparable glucose kinetics and low shear stress in both chambers. An optimized flow rate did not alter islet β-cell electrical activity or coupling in response to glucose. Culturing for up to 8 days did not change islet survival as well as glucose-induced electrical or secretory kinetics of islet β-cells. The addition of a physiological amino acid mix, in the presence of elevated glucose, made a considerable change in the functional organisation of islet β-cell activity in terms of frequency and coupling, which explains the ensuing strong increase in insulin secretion. This device thus allows reliable long-term multiparametric on-line monitoring in two islet populations. The ease of fabrication, assembly and handling should permit widespread long-term on-line monitoring of islet activity in native micro-organs (e.g. controls/mutants), pseudo-islets or stem-cell-derived islet-like organoids.
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