Protein-Mediated Interactions of Pancreatic Islet Cells

The islets of Langerhans collectively form the endocrine pancreas, the organ that is soley responsible for insulin secretion in mammals, and which plays a prominent role in the control of circulating glucose and metabolism. Normal function of these islets implies the coordination of different types...

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Main Author: Paolo Meda
Format: Article
Language:English
Published: Wiley 2013-01-01
Series:Scientifica
Online Access:http://dx.doi.org/10.1155/2013/621249
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author Paolo Meda
author_facet Paolo Meda
author_sort Paolo Meda
collection DOAJ
description The islets of Langerhans collectively form the endocrine pancreas, the organ that is soley responsible for insulin secretion in mammals, and which plays a prominent role in the control of circulating glucose and metabolism. Normal function of these islets implies the coordination of different types of endocrine cells, noticeably of the beta cells which produce insulin. Given that an appropriate secretion of this hormone is vital to the organism, a number of mechanisms have been selected during evolution, which now converge to coordinate beta cell functions. Among these, several mechanisms depend on different families of integral membrane proteins, which ensure direct (cadherins, N-CAM, occludin, and claudins) and paracrine communications (pannexins) between beta cells, and between these cells and the other islet cell types. Also, other proteins (integrins) provide communication of the different islet cell types with the materials that form the islet basal laminae and extracellular matrix. Here, we review what is known about these proteins and their signaling in pancreatic β-cells, with particular emphasis on the signaling provided by Cx36, given that this is the integral membrane protein involved in cell-to-cell communication, which has so far been mostly investigated for effects on beta cell functions.
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spelling doaj-art-cb64c3cfe48e4d27894220745b9483a12025-02-03T00:59:27ZengWileyScientifica2090-908X2013-01-01201310.1155/2013/621249621249Protein-Mediated Interactions of Pancreatic Islet CellsPaolo Meda0Department of Cell Physiology and Metabolism, University of Geneva School of Medicine, 1 rue Michel-Servet, 1211 Geneva 4, SwitzerlandThe islets of Langerhans collectively form the endocrine pancreas, the organ that is soley responsible for insulin secretion in mammals, and which plays a prominent role in the control of circulating glucose and metabolism. Normal function of these islets implies the coordination of different types of endocrine cells, noticeably of the beta cells which produce insulin. Given that an appropriate secretion of this hormone is vital to the organism, a number of mechanisms have been selected during evolution, which now converge to coordinate beta cell functions. Among these, several mechanisms depend on different families of integral membrane proteins, which ensure direct (cadherins, N-CAM, occludin, and claudins) and paracrine communications (pannexins) between beta cells, and between these cells and the other islet cell types. Also, other proteins (integrins) provide communication of the different islet cell types with the materials that form the islet basal laminae and extracellular matrix. Here, we review what is known about these proteins and their signaling in pancreatic β-cells, with particular emphasis on the signaling provided by Cx36, given that this is the integral membrane protein involved in cell-to-cell communication, which has so far been mostly investigated for effects on beta cell functions.http://dx.doi.org/10.1155/2013/621249
spellingShingle Paolo Meda
Protein-Mediated Interactions of Pancreatic Islet Cells
Scientifica
title Protein-Mediated Interactions of Pancreatic Islet Cells
title_full Protein-Mediated Interactions of Pancreatic Islet Cells
title_fullStr Protein-Mediated Interactions of Pancreatic Islet Cells
title_full_unstemmed Protein-Mediated Interactions of Pancreatic Islet Cells
title_short Protein-Mediated Interactions of Pancreatic Islet Cells
title_sort protein mediated interactions of pancreatic islet cells
url http://dx.doi.org/10.1155/2013/621249
work_keys_str_mv AT paolomeda proteinmediatedinteractionsofpancreaticisletcells