Beta Cell Store-Operated Ion Channels

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Islets of Langerhans, 2. ed.

Abstract

Signaling molecules produced in the pancreatic β-cell following mitochondrial oxidation of glycolytic intermediate metabolites and oxidative phosphorylation trigger Ca2+-dependent signaling pathways that regulate insulin exocytosis. Much is known about ATP-sensitive K+ and voltage-gated Ca2+ currents that contribute to Ca2+-dependent signal transduction in β-cells and insulin secretion, but relatively little is known about other Ca2+ channels that regulate β-cell Ca2+ signaling dynamics and insulin secretion. In a wide range of eukaryotic cells, store-operated Ca2+ entry (SOCE) plays a critical role regulating spatial and temporal changes in cytoplasmic Ca2+ concentration, endoplasmic reticulum (ER) Ca2+ homeostasis, gene expression, protein biosynthesis, and cell viability. Although SOCE has been proposed to play important roles in β-cell Ca2+ signaling and insulin secretion, the underlying molecular mechanisms remain undefined. In this chapter, we provide both an overview of our current understanding of ionic currents regulated by ER Ca2+ stores in insulin-secreting cells and a review of studies in other cell systems that have identified the molecular basis and regulation of SOCE.

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Acknowledgments

Research in the authors’ laboratories was supported by the American Diabetes Association Research Award 1-12-BS-109 (CAL) and by the National Institutes of Health R01 grants DK074966 and DK092616 (MWR).

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Correspondence to Michael Wm. Roe .

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Leech, C.A., Kopp, R.F., Philipson, L.H., Roe, M.W. (2014). Beta Cell Store-Operated Ion Channels . In: Islam, M. (eds) Islets of Langerhans, 2. ed.. Springer, Dordrecht. https://doi.org/10.1007/978-94-007-6884-0_40-2

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  • DOI: https://doi.org/10.1007/978-94-007-6884-0_40-2

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