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• W2062783006 abstract "The pancreatic islet is a highly coupled, multicellular system that exhibits complex spatiotemporal electrical activity in response to elevated glucose levels. The emergent properties of islets, which differ from those arising in isolated islet cells, are believed to arise in part by gap junctional coupling, but the mechanisms through which this coupling occurs are poorly understood. To uncover these mechanisms, we have used both high-speed imaging and theoretical modeling of the electrical activity in pancreatic islets under a reduction in the gap junction mediated electrical coupling. Utilizing islets from a gap junction protein connexin 36 knockout mouse model together with chemical inhibitors, we can modulate the electrical coupling in the islet in a precise manner and quantify this modulation by electrophysiology measurements. We find that after a reduction in electrical coupling, calcium waves are slowed as well as disrupted, and the number of cells showing synchronous calcium oscillations is reduced. This behavior can be reproduced by computational modeling of a heterogeneous population of beta-cells with heterogeneous levels of electrical coupling. The resulting quantitative agreement between the data and analytical models of islet connectivity, using only a single free parameter, reveals the mechanistic underpinnings of the multicellular behavior of the islet." @default.
• W2062783006 created "2016-06-24" @default.
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• W2062783006 date "2008-12-01" @default.
• W2062783006 modified "2023-10-12" @default.
• W2062783006 title "Gap Junction Coupling and Calcium Waves in the Pancreatic Islet" @default.
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• W2062783006 doi "https://doi.org/10.1529/biophysj.108.140863" @default.
• W2062783006 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/2586567" @default.
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