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Assay for high glucose-mediated islet cell sensitization to apoptosis induced by streptozotocin and cytokines

Pancreatic β-cell apoptosis is known to participate in the β-cell destruction process that occurs in diabetes. It has been described that high glucose level induces a hyperfunctional status which could provoke apoptosis. This phenomenon is known as glucotoxicity and has been proposed that it can pla...

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Detalles Bibliográficos
Autores principales: Mellado-Gil, Jose M., Aguilar-Diosdado, Manuel
Formato: Texto
Lenguaje:English
Publicado: Biological Procedures Online 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1280327/
https://www.ncbi.nlm.nih.gov/pubmed/16281079
http://dx.doi.org/10.1251/bpo113
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author Mellado-Gil, Jose M.
Aguilar-Diosdado, Manuel
author_facet Mellado-Gil, Jose M.
Aguilar-Diosdado, Manuel
author_sort Mellado-Gil, Jose M.
collection PubMed
description Pancreatic β-cell apoptosis is known to participate in the β-cell destruction process that occurs in diabetes. It has been described that high glucose level induces a hyperfunctional status which could provoke apoptosis. This phenomenon is known as glucotoxicity and has been proposed that it can play a role in type 1 diabetes mellitus pathogenesis. In this study we develop an experimental design to sensitize pancreatic islet cells by high glucose to streptozotocin (STZ) and proinflammatory cytokines [interleukin (IL)-1β, tumor necrosis factor (TNF)-α and interferon (IFN)-γ]-induced apoptosis. This method is appropriate for subsequent quantification of apoptotic islet cells stained with Tdt-mediated dUTP Nick-End Labeling (TUNEL) and protein expression assays by Western Blotting (WB).
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spelling pubmed-12803272005-11-09 Assay for high glucose-mediated islet cell sensitization to apoptosis induced by streptozotocin and cytokines Mellado-Gil, Jose M. Aguilar-Diosdado, Manuel Biol Proced Online Research Article Pancreatic β-cell apoptosis is known to participate in the β-cell destruction process that occurs in diabetes. It has been described that high glucose level induces a hyperfunctional status which could provoke apoptosis. This phenomenon is known as glucotoxicity and has been proposed that it can play a role in type 1 diabetes mellitus pathogenesis. In this study we develop an experimental design to sensitize pancreatic islet cells by high glucose to streptozotocin (STZ) and proinflammatory cytokines [interleukin (IL)-1β, tumor necrosis factor (TNF)-α and interferon (IFN)-γ]-induced apoptosis. This method is appropriate for subsequent quantification of apoptotic islet cells stained with Tdt-mediated dUTP Nick-End Labeling (TUNEL) and protein expression assays by Western Blotting (WB). Biological Procedures Online 2005-11-07 /pmc/articles/PMC1280327/ /pubmed/16281079 http://dx.doi.org/10.1251/bpo113 Text en Copyright © November 11, 2005, JM Mellado-Gil et al. This paper is Open Access and is published in Biological Procedures Online under license from the authors. Copying, printing, redistribution and storage permitted.
spellingShingle Research Article
Mellado-Gil, Jose M.
Aguilar-Diosdado, Manuel
Assay for high glucose-mediated islet cell sensitization to apoptosis induced by streptozotocin and cytokines
title Assay for high glucose-mediated islet cell sensitization to apoptosis induced by streptozotocin and cytokines
title_full Assay for high glucose-mediated islet cell sensitization to apoptosis induced by streptozotocin and cytokines
title_fullStr Assay for high glucose-mediated islet cell sensitization to apoptosis induced by streptozotocin and cytokines
title_full_unstemmed Assay for high glucose-mediated islet cell sensitization to apoptosis induced by streptozotocin and cytokines
title_short Assay for high glucose-mediated islet cell sensitization to apoptosis induced by streptozotocin and cytokines
title_sort assay for high glucose-mediated islet cell sensitization to apoptosis induced by streptozotocin and cytokines
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1280327/
https://www.ncbi.nlm.nih.gov/pubmed/16281079
http://dx.doi.org/10.1251/bpo113
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