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The Calpain, Caspase 12, Caspase 3 Cascade Leading to Apoptosis Is Altered in F508del-CFTR Expressing Cells

In cystic fibrosis (CF), the most frequent mutant variant of the cystic fibrosis transmembrane conductance regulator (CFTR), F508del-CFTR protein, is misfolded and retained in the endoplasmic reticulum (ER). We previously showed that the unfolded protein response (UPR) may be triggered in CF. Since...

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Autores principales: Kerbiriou, Mathieu, Teng, Ling, Benz, Nathalie, Trouvé, Pascal, Férec, Claude
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2793515/
https://www.ncbi.nlm.nih.gov/pubmed/20041182
http://dx.doi.org/10.1371/journal.pone.0008436
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author Kerbiriou, Mathieu
Teng, Ling
Benz, Nathalie
Trouvé, Pascal
Férec, Claude
author_facet Kerbiriou, Mathieu
Teng, Ling
Benz, Nathalie
Trouvé, Pascal
Férec, Claude
author_sort Kerbiriou, Mathieu
collection PubMed
description In cystic fibrosis (CF), the most frequent mutant variant of the cystic fibrosis transmembrane conductance regulator (CFTR), F508del-CFTR protein, is misfolded and retained in the endoplasmic reticulum (ER). We previously showed that the unfolded protein response (UPR) may be triggered in CF. Since prolonged UPR activation leads to apoptosis via the calcium-calpain-caspase-12-caspase-3 cascade and because apoptosis is altered in CF, our aim was to compare the ER stress-induced apoptosis pathway between wild type (Wt) and F508del-CFTR expressing cells. Here we show that the calcium-calpain-caspase-12-caspase-3 cascade is altered in F508del-CFTR expressing cells. We propose that this alteration is involved in the altered apoptosis triggering observed in CF.
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spelling pubmed-27935152009-12-30 The Calpain, Caspase 12, Caspase 3 Cascade Leading to Apoptosis Is Altered in F508del-CFTR Expressing Cells Kerbiriou, Mathieu Teng, Ling Benz, Nathalie Trouvé, Pascal Férec, Claude PLoS One Research Article In cystic fibrosis (CF), the most frequent mutant variant of the cystic fibrosis transmembrane conductance regulator (CFTR), F508del-CFTR protein, is misfolded and retained in the endoplasmic reticulum (ER). We previously showed that the unfolded protein response (UPR) may be triggered in CF. Since prolonged UPR activation leads to apoptosis via the calcium-calpain-caspase-12-caspase-3 cascade and because apoptosis is altered in CF, our aim was to compare the ER stress-induced apoptosis pathway between wild type (Wt) and F508del-CFTR expressing cells. Here we show that the calcium-calpain-caspase-12-caspase-3 cascade is altered in F508del-CFTR expressing cells. We propose that this alteration is involved in the altered apoptosis triggering observed in CF. Public Library of Science 2009-12-24 /pmc/articles/PMC2793515/ /pubmed/20041182 http://dx.doi.org/10.1371/journal.pone.0008436 Text en Kerbiriou et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Kerbiriou, Mathieu
Teng, Ling
Benz, Nathalie
Trouvé, Pascal
Férec, Claude
The Calpain, Caspase 12, Caspase 3 Cascade Leading to Apoptosis Is Altered in F508del-CFTR Expressing Cells
title The Calpain, Caspase 12, Caspase 3 Cascade Leading to Apoptosis Is Altered in F508del-CFTR Expressing Cells
title_full The Calpain, Caspase 12, Caspase 3 Cascade Leading to Apoptosis Is Altered in F508del-CFTR Expressing Cells
title_fullStr The Calpain, Caspase 12, Caspase 3 Cascade Leading to Apoptosis Is Altered in F508del-CFTR Expressing Cells
title_full_unstemmed The Calpain, Caspase 12, Caspase 3 Cascade Leading to Apoptosis Is Altered in F508del-CFTR Expressing Cells
title_short The Calpain, Caspase 12, Caspase 3 Cascade Leading to Apoptosis Is Altered in F508del-CFTR Expressing Cells
title_sort calpain, caspase 12, caspase 3 cascade leading to apoptosis is altered in f508del-cftr expressing cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2793515/
https://www.ncbi.nlm.nih.gov/pubmed/20041182
http://dx.doi.org/10.1371/journal.pone.0008436
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