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Caspase deficiency alters the murine gut microbiome
Caspases are aspartate-specific cysteine proteases that have an essential role in apoptosis and inflammation, and contribute to the maintenance of homeostasis in the intestine. These facts, together with the knowledge that caspases are implicated in host-microbe crosstalk, prompted us to investigate...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3219086/ https://www.ncbi.nlm.nih.gov/pubmed/22012254 http://dx.doi.org/10.1038/cddis.2011.101 |
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author | Brinkman, B M Hildebrand, F Kubica, M Goosens, D Del Favero, J Declercq, W Raes, J Vandenabeele, P |
author_facet | Brinkman, B M Hildebrand, F Kubica, M Goosens, D Del Favero, J Declercq, W Raes, J Vandenabeele, P |
author_sort | Brinkman, B M |
collection | PubMed |
description | Caspases are aspartate-specific cysteine proteases that have an essential role in apoptosis and inflammation, and contribute to the maintenance of homeostasis in the intestine. These facts, together with the knowledge that caspases are implicated in host-microbe crosstalk, prompted us to investigate the effect of caspase (Casp)1, -3 and -7 deficiency on the composition of the murine gut microbiota. We observed significant changes in the abundance of the Firmicutes and Bacteroidetes phyla, in particular the Lachnospiraceae, Porphyromonodaceae and Prevotellacea families, when comparing Casp-1, -7 and -3 knockout mice with wild-type mice. Our data point toward an intricate relationship between these caspases and the composition of the murine gut microflora. |
format | Online Article Text |
id | pubmed-3219086 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-32190862011-12-09 Caspase deficiency alters the murine gut microbiome Brinkman, B M Hildebrand, F Kubica, M Goosens, D Del Favero, J Declercq, W Raes, J Vandenabeele, P Cell Death Dis Original Article Caspases are aspartate-specific cysteine proteases that have an essential role in apoptosis and inflammation, and contribute to the maintenance of homeostasis in the intestine. These facts, together with the knowledge that caspases are implicated in host-microbe crosstalk, prompted us to investigate the effect of caspase (Casp)1, -3 and -7 deficiency on the composition of the murine gut microbiota. We observed significant changes in the abundance of the Firmicutes and Bacteroidetes phyla, in particular the Lachnospiraceae, Porphyromonodaceae and Prevotellacea families, when comparing Casp-1, -7 and -3 knockout mice with wild-type mice. Our data point toward an intricate relationship between these caspases and the composition of the murine gut microflora. Nature Publishing Group 2011-10 2011-10-20 /pmc/articles/PMC3219086/ /pubmed/22012254 http://dx.doi.org/10.1038/cddis.2011.101 Text en Copyright © 2011 Macmillan Publishers Limited http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under the Creative Commons Attribution-NonCommercial-No Derivative Works 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/ |
spellingShingle | Original Article Brinkman, B M Hildebrand, F Kubica, M Goosens, D Del Favero, J Declercq, W Raes, J Vandenabeele, P Caspase deficiency alters the murine gut microbiome |
title | Caspase deficiency alters the murine gut microbiome |
title_full | Caspase deficiency alters the murine gut microbiome |
title_fullStr | Caspase deficiency alters the murine gut microbiome |
title_full_unstemmed | Caspase deficiency alters the murine gut microbiome |
title_short | Caspase deficiency alters the murine gut microbiome |
title_sort | caspase deficiency alters the murine gut microbiome |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3219086/ https://www.ncbi.nlm.nih.gov/pubmed/22012254 http://dx.doi.org/10.1038/cddis.2011.101 |
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