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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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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Hindawi Publishing Corporation
2013
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3820362/ https://www.ncbi.nlm.nih.gov/pubmed/24278783 http://dx.doi.org/10.1155/2013/621249 |
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author | Meda, Paolo |
author_facet | Meda, Paolo |
author_sort | Meda, Paolo |
collection | PubMed |
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. |
format | Online Article Text |
id | pubmed-3820362 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-38203622013-11-25 Protein-Mediated Interactions of Pancreatic Islet Cells Meda, Paolo Scientifica (Cairo) Review Article 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. Hindawi Publishing Corporation 2013 2013-01-08 /pmc/articles/PMC3820362/ /pubmed/24278783 http://dx.doi.org/10.1155/2013/621249 Text en Copyright © 2013 Paolo Meda. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Meda, Paolo Protein-Mediated Interactions of Pancreatic Islet Cells |
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 |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3820362/ https://www.ncbi.nlm.nih.gov/pubmed/24278783 http://dx.doi.org/10.1155/2013/621249 |
work_keys_str_mv | AT medapaolo proteinmediatedinteractionsofpancreaticisletcells |