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<metadata xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dc="http://purl.org/dc/elements/1.1/"><dc:title>The relationship between membrane potential and calcium dynamics in glucose-stimulated beta cell syncytium in acute mouse pancreas tissue slices</dc:title><dc:creator>Dolenšek,	Jurij	(Avtor)
	</dc:creator><dc:creator>Stožer,	Andraž	(Avtor)
	</dc:creator><dc:creator>Skelin,	Maša	(Avtor)
	</dc:creator><dc:creator>Miller,	Evan	(Avtor)
	</dc:creator><dc:creator>Rupnik,	Marjan	(Avtor)
	</dc:creator><dc:subject>glucose</dc:subject><dc:subject>pancreas</dc:subject><dc:subject>mice</dc:subject><dc:description>Oscillatory electrical activity is regarded as a hallmark of the pancreatic beta cell glucose-dependent excitability pattern. Electrophysiologically recorded membrane potential oscillations in beta cells are associated with in-phase oscillatory cytosolic calcium activity ([Ca2+]i) measured with fluorescent probes. Recent high spatial and temporal resolution confocal imaging revealed that glucose stimulation of beta cells in intact islets within acute tissue slices produces a [Ca2+]i change with initial transient phase followed by a plateau phase with highly synchronized [Ca2+]i oscillations. Here, we aimed to correlate the plateau [Ca2+]i oscillations with the oscillations of membrane potential using patch-clamp and for the first time high resolution voltage-sensitive dye based confocal imaging. Our results demonstrated that the glucose-evoked membrane potential oscillations spread over the islet in a wave-like manner, their durations and wave velocities being comparable to the ones for [Ca2+]i oscillations and waves. High temporal resolution simultaneous records of membrane potential and [Ca2+]i confirmed tight but nevertheless limited coupling of the two processes, with membrane depolarization preceding the [Ca2+]i increase. The potassium channel blocker tetraethylammonium increased the velocity at which oscillations advanced over the islet by several-fold while, at the same time, emphasized differences in kinetics of the membrane potential and the [Ca2+]i. The combination of both imaging techniques provides a powerful tool that will help us attain deeper knowledge of the beta cell network.</dc:description><dc:date>2013</dc:date><dc:date>2017-06-19 13:31:19</dc:date><dc:type>Znanstveno delo</dc:type><dc:identifier>66303</dc:identifier><dc:identifier>ISSN: 1932-6203</dc:identifier><dc:identifier>UDK: 612.349.7</dc:identifier><dc:identifier>OceCobissID: 2005896</dc:identifier><dc:identifier>COBISS_ID: 512362552</dc:identifier><dc:identifier>DOI: 10.1371/journal.pone.0082374</dc:identifier><dc:identifier>ISSN pri članku: 1932-6203</dc:identifier><dc:identifier>NUK URN: URN:SI:UM:DK:H6SGPS3R</dc:identifier><dc:language>sl</dc:language></metadata>
