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Chemical Methods to Induce Beta-Cell Proliferation
Pancreatic beta-cell regeneration, for example, by inducing proliferation, remains an important goal in developing effective treatments for diabetes. However, beta cells have mainly been considered quiescent. This “static” view has recently been challenged by observations of relevant physiological c...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3395230/ https://www.ncbi.nlm.nih.gov/pubmed/22811709 http://dx.doi.org/10.1155/2012/925143 |
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author | Vetere, Amedeo Wagner, Bridget K. |
author_facet | Vetere, Amedeo Wagner, Bridget K. |
author_sort | Vetere, Amedeo |
collection | PubMed |
description | Pancreatic beta-cell regeneration, for example, by inducing proliferation, remains an important goal in developing effective treatments for diabetes. However, beta cells have mainly been considered quiescent. This “static” view has recently been challenged by observations of relevant physiological conditions in which metabolic stress is compensated by an increase in beta-cell mass. Understanding the molecular mechanisms underlining these process could open the possibility of developing novel small molecules to increase beta-cell mass. Several cellular cell-cycle and signaling proteins provide attractive targets for high throughput screening, and recent advances in cell culture have enabled phenotypic screening for small molecule-induced beta-cell proliferation. We present here an overview of the current trends involving small-molecule approaches to induce beta-cell regeneration by proliferation. |
format | Online Article Text |
id | pubmed-3395230 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-33952302012-07-18 Chemical Methods to Induce Beta-Cell Proliferation Vetere, Amedeo Wagner, Bridget K. Int J Endocrinol Review Article Pancreatic beta-cell regeneration, for example, by inducing proliferation, remains an important goal in developing effective treatments for diabetes. However, beta cells have mainly been considered quiescent. This “static” view has recently been challenged by observations of relevant physiological conditions in which metabolic stress is compensated by an increase in beta-cell mass. Understanding the molecular mechanisms underlining these process could open the possibility of developing novel small molecules to increase beta-cell mass. Several cellular cell-cycle and signaling proteins provide attractive targets for high throughput screening, and recent advances in cell culture have enabled phenotypic screening for small molecule-induced beta-cell proliferation. We present here an overview of the current trends involving small-molecule approaches to induce beta-cell regeneration by proliferation. Hindawi Publishing Corporation 2012 2012-06-28 /pmc/articles/PMC3395230/ /pubmed/22811709 http://dx.doi.org/10.1155/2012/925143 Text en Copyright © 2012 A. Vetere and B. K. Wagner. 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 Vetere, Amedeo Wagner, Bridget K. Chemical Methods to Induce Beta-Cell Proliferation |
title | Chemical Methods to Induce Beta-Cell Proliferation |
title_full | Chemical Methods to Induce Beta-Cell Proliferation |
title_fullStr | Chemical Methods to Induce Beta-Cell Proliferation |
title_full_unstemmed | Chemical Methods to Induce Beta-Cell Proliferation |
title_short | Chemical Methods to Induce Beta-Cell Proliferation |
title_sort | chemical methods to induce beta-cell proliferation |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3395230/ https://www.ncbi.nlm.nih.gov/pubmed/22811709 http://dx.doi.org/10.1155/2012/925143 |
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