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Identification of Small Molecules That Protect Pancreatic β Cells against Endoplasmic Reticulum Stress-Induced Cell Death
[Image: see text] Endoplasmic reticulum (ER) stress plays an important role in the decline in pancreatic β cell function and mass observed in type 2 diabetes. Here, we developed a novel β cell-based high-throughput screening assay to identify small molecules that protect β cells against ER stress-in...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4273981/ https://www.ncbi.nlm.nih.gov/pubmed/25279668 http://dx.doi.org/10.1021/cb500740d |
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author | Tran, Kim Li, Yu Duan, Hongliang Arora, Daleep Lim, Hui-Ying Wang, Weidong |
author_facet | Tran, Kim Li, Yu Duan, Hongliang Arora, Daleep Lim, Hui-Ying Wang, Weidong |
author_sort | Tran, Kim |
collection | PubMed |
description | [Image: see text] Endoplasmic reticulum (ER) stress plays an important role in the decline in pancreatic β cell function and mass observed in type 2 diabetes. Here, we developed a novel β cell-based high-throughput screening assay to identify small molecules that protect β cells against ER stress-induced cell death. Mouse βTC6 cells were treated with the ER stressor tunicamycin to induce ER stress, and cell death was measured as a reduction in cellular ATP. A collection of 17600 compounds was screened for molecules that promote β cell survival. Of the approximately 80 positive hits, two selected compounds were able to increase the survival of human primary β cells and rodent β cell lines subjected to ER stressors including palmitate, a free fatty acid of pathological relevance to diabetes. These compounds also restored ER stress-impaired glucose-stimulated insulin secretion responses. We show that the compounds promote β cell survival by reducing the expression of key genes of the unfolded protein response and apoptosis, thus alleviating ER stress. Identification of small molecules that prevent ER stress-induced β cell dysfunction and death may provide a new modality for the treatment of diabetes. |
format | Online Article Text |
id | pubmed-4273981 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-42739812015-10-03 Identification of Small Molecules That Protect Pancreatic β Cells against Endoplasmic Reticulum Stress-Induced Cell Death Tran, Kim Li, Yu Duan, Hongliang Arora, Daleep Lim, Hui-Ying Wang, Weidong ACS Chem Biol [Image: see text] Endoplasmic reticulum (ER) stress plays an important role in the decline in pancreatic β cell function and mass observed in type 2 diabetes. Here, we developed a novel β cell-based high-throughput screening assay to identify small molecules that protect β cells against ER stress-induced cell death. Mouse βTC6 cells were treated with the ER stressor tunicamycin to induce ER stress, and cell death was measured as a reduction in cellular ATP. A collection of 17600 compounds was screened for molecules that promote β cell survival. Of the approximately 80 positive hits, two selected compounds were able to increase the survival of human primary β cells and rodent β cell lines subjected to ER stressors including palmitate, a free fatty acid of pathological relevance to diabetes. These compounds also restored ER stress-impaired glucose-stimulated insulin secretion responses. We show that the compounds promote β cell survival by reducing the expression of key genes of the unfolded protein response and apoptosis, thus alleviating ER stress. Identification of small molecules that prevent ER stress-induced β cell dysfunction and death may provide a new modality for the treatment of diabetes. American Chemical Society 2014-10-03 2014-12-19 /pmc/articles/PMC4273981/ /pubmed/25279668 http://dx.doi.org/10.1021/cb500740d Text en Copyright © 2014 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Tran, Kim Li, Yu Duan, Hongliang Arora, Daleep Lim, Hui-Ying Wang, Weidong Identification of Small Molecules That Protect Pancreatic β Cells against Endoplasmic Reticulum Stress-Induced Cell Death |
title | Identification of Small Molecules That Protect Pancreatic
β Cells against Endoplasmic Reticulum Stress-Induced Cell Death |
title_full | Identification of Small Molecules That Protect Pancreatic
β Cells against Endoplasmic Reticulum Stress-Induced Cell Death |
title_fullStr | Identification of Small Molecules That Protect Pancreatic
β Cells against Endoplasmic Reticulum Stress-Induced Cell Death |
title_full_unstemmed | Identification of Small Molecules That Protect Pancreatic
β Cells against Endoplasmic Reticulum Stress-Induced Cell Death |
title_short | Identification of Small Molecules That Protect Pancreatic
β Cells against Endoplasmic Reticulum Stress-Induced Cell Death |
title_sort | identification of small molecules that protect pancreatic
β cells against endoplasmic reticulum stress-induced cell death |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4273981/ https://www.ncbi.nlm.nih.gov/pubmed/25279668 http://dx.doi.org/10.1021/cb500740d |
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