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High-level integration of murine intestinal transcriptomics data highlights the importance of the complement system in mucosal homeostasis
BACKGROUND: The mammalian intestine is a complex biological system that exhibits functional plasticity in its response to diverse stimuli to maintain homeostasis. To improve our understanding of this plasticity, we performed a high-level data integration of 14 whole-genome transcriptomics datasets f...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6937694/ https://www.ncbi.nlm.nih.gov/pubmed/31888466 http://dx.doi.org/10.1186/s12864-019-6390-x |
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author | Benis, Nirupama Wells, Jerry M. Smits, Mari A. Kar, Soumya Kanti van der Hee, Bart dos Santos, Vitor A. P. Martins Suarez-Diez, Maria Schokker, Dirkjan |
author_facet | Benis, Nirupama Wells, Jerry M. Smits, Mari A. Kar, Soumya Kanti van der Hee, Bart dos Santos, Vitor A. P. Martins Suarez-Diez, Maria Schokker, Dirkjan |
author_sort | Benis, Nirupama |
collection | PubMed |
description | BACKGROUND: The mammalian intestine is a complex biological system that exhibits functional plasticity in its response to diverse stimuli to maintain homeostasis. To improve our understanding of this plasticity, we performed a high-level data integration of 14 whole-genome transcriptomics datasets from samples of intestinal mouse mucosa. We used the tool Centrality based Pathway Analysis (CePa), along with information from the Reactome database. RESULTS: The results show an integrated response of the mouse intestinal mucosa to challenges with agents introduced orally that were expected to perturb homeostasis. We observed that a common set of pathways respond to different stimuli, of which the most reactive was the Regulation of Complement Cascade pathway. Altered expression of the Regulation of Complement Cascade pathway was verified in mouse organoids challenged with different stimuli in vitro. CONCLUSIONS: Results of the integrated transcriptomics analysis and data driven experiment suggest an important role of epithelial production of complement and host complement defence factors in the maintenance of homeostasis. |
format | Online Article Text |
id | pubmed-6937694 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-69376942019-12-31 High-level integration of murine intestinal transcriptomics data highlights the importance of the complement system in mucosal homeostasis Benis, Nirupama Wells, Jerry M. Smits, Mari A. Kar, Soumya Kanti van der Hee, Bart dos Santos, Vitor A. P. Martins Suarez-Diez, Maria Schokker, Dirkjan BMC Genomics Research Article BACKGROUND: The mammalian intestine is a complex biological system that exhibits functional plasticity in its response to diverse stimuli to maintain homeostasis. To improve our understanding of this plasticity, we performed a high-level data integration of 14 whole-genome transcriptomics datasets from samples of intestinal mouse mucosa. We used the tool Centrality based Pathway Analysis (CePa), along with information from the Reactome database. RESULTS: The results show an integrated response of the mouse intestinal mucosa to challenges with agents introduced orally that were expected to perturb homeostasis. We observed that a common set of pathways respond to different stimuli, of which the most reactive was the Regulation of Complement Cascade pathway. Altered expression of the Regulation of Complement Cascade pathway was verified in mouse organoids challenged with different stimuli in vitro. CONCLUSIONS: Results of the integrated transcriptomics analysis and data driven experiment suggest an important role of epithelial production of complement and host complement defence factors in the maintenance of homeostasis. BioMed Central 2019-12-30 /pmc/articles/PMC6937694/ /pubmed/31888466 http://dx.doi.org/10.1186/s12864-019-6390-x Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Benis, Nirupama Wells, Jerry M. Smits, Mari A. Kar, Soumya Kanti van der Hee, Bart dos Santos, Vitor A. P. Martins Suarez-Diez, Maria Schokker, Dirkjan High-level integration of murine intestinal transcriptomics data highlights the importance of the complement system in mucosal homeostasis |
title | High-level integration of murine intestinal transcriptomics data highlights the importance of the complement system in mucosal homeostasis |
title_full | High-level integration of murine intestinal transcriptomics data highlights the importance of the complement system in mucosal homeostasis |
title_fullStr | High-level integration of murine intestinal transcriptomics data highlights the importance of the complement system in mucosal homeostasis |
title_full_unstemmed | High-level integration of murine intestinal transcriptomics data highlights the importance of the complement system in mucosal homeostasis |
title_short | High-level integration of murine intestinal transcriptomics data highlights the importance of the complement system in mucosal homeostasis |
title_sort | high-level integration of murine intestinal transcriptomics data highlights the importance of the complement system in mucosal homeostasis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6937694/ https://www.ncbi.nlm.nih.gov/pubmed/31888466 http://dx.doi.org/10.1186/s12864-019-6390-x |
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