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Please use this identifier to cite or link to this item: http://hdl.handle.net/10261/39106
Title: Pancreatic islet cells: a model for calcium-dependent peptide release
Authors: Soria Escoms, Bernat; Hmadcha, Abdelkrim; Martín, Franz; Quesada, Ivan
Issue Date: Apr-2010
Publisher: Human frontier science program
Citation: HFSP Journal 4(2): 52-60 (2010)
Abstract: In mammals the concentration of blood glucose is kept close to 5 mmol/l. Different cell types in the islet of Langerhans participate in the control of glucose homeostasis. β-cells, the most frequent type in pancreatic islets, are responsible for the synthesis, storage, and release of insulin. Insulin, released with increases in blood glucose promotes glucose uptake into the cells. In response to glucose changes, pancreatic α-, β-, and δ-cells regulate their electrical activity and Ca2+ signals to release glucagon, insulin, and somatostatin, respectively. While all these signaling steps are stimulated in hypoglycemic conditions in α-cells, the activation of these events require higher glucose concentrations in β and also in δ-cells. The stimulus-secretion coupling process and intracellular Ca2+ ([Ca2+]i) dynamics that allow β-cells to secrete is well-accepted. Conversely, the mechanisms that regulate α- and δ-cell secretion are still under study. Here, we will consider the glucose-induced signaling mechanisms in each cell type and the mathematical models that explain Ca2+ dynamics.
Description: 9 páginas, 4 figuras.-- et al.
Publisher version (URL): http://dx.doi.org/10.2976/1.3364560
URI: http://hdl.handle.net/10261/39106
DOI: 10.2976/1.3364560
ISSN: 1955-2068
E-ISSN: 1955-205X
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