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Importance of the interferon-α system in murine large intestine indicated by microarray analysis of commensal bacteria-induced immunological changes
BACKGROUND: Although microbiota play a critical role in the normal development and function of host immune systems, the underlying mechanisms, especially those involved in the large intestine (LI), remain unknown. In the present study, we performed transcriptome analysis of the LI of germ-free (GF)...
Autores principales: | , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2408602/ https://www.ncbi.nlm.nih.gov/pubmed/18439305 http://dx.doi.org/10.1186/1471-2164-9-192 |
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author | Munakata, Kaori Yamamoto, Masahiro Anjiki, Naoko Nishiyama, Mitsue Imamura, Sachiko Iizuka, Seiichi Takashima, Kiyoe Ishige, Atsushi Hioki, Kyoji Ohnishi, Yasuyuki Watanabe, Kenji |
author_facet | Munakata, Kaori Yamamoto, Masahiro Anjiki, Naoko Nishiyama, Mitsue Imamura, Sachiko Iizuka, Seiichi Takashima, Kiyoe Ishige, Atsushi Hioki, Kyoji Ohnishi, Yasuyuki Watanabe, Kenji |
author_sort | Munakata, Kaori |
collection | PubMed |
description | BACKGROUND: Although microbiota play a critical role in the normal development and function of host immune systems, the underlying mechanisms, especially those involved in the large intestine (LI), remain unknown. In the present study, we performed transcriptome analysis of the LI of germ-free (GF) and specific pathogen-free (SPF) mice of the IQI strain, an inbred strain established from ICR mice. RESULTS: GeneChip analysis, quantitative real-time RT-PCR, and reconfirmation using bacteria-inoculated GF mice revealed differences in the expression levels of several immune-related genes, such as cryptdin-related sequences (CRS), certain subsets of type 1 interferon (IFN)-related genes, class Ib MHC molecules, and certain complements. LI expressed no authentic cryptdins but predominantly expressed CRS2, 4, and 7. The mRNA levels of IFN-related genes, including Irf7, Isgf3g, Ifit1 and Stat1, were lower in SPF- and flora-reconstituted mice. When an oral IFN-α inducer tilorone analog, R11567DA, was administered to SPF mice, IFN-α was induced rapidly in the LI at 4 h, whereas no IFN-α protein was detected in the small intestine (SI) or blood. In situ hybridization and immunohistochemistry suggested that the IFN-α production originated from Paneth cells in the SI, and portions of lamina proprial CD11b- or mPDCA1-positive cells in the LI. CONCLUSION: The present study suggests that microbial colonization, while inducing the expression of anti-microbial peptides, results in the down-regulation of certain genes responsible for immune responses, especially for type I IFN synthesis. This may reflect the adaptation process of the immune system in the LI to prevent excessive inflammation with respect to continuous microbial exposure. Further, the repertoire of anti-microbial peptides and the extraordinary role of interferon producing cells in the LI have been found to be distinct from those in the SI. |
format | Text |
id | pubmed-2408602 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-24086022008-05-31 Importance of the interferon-α system in murine large intestine indicated by microarray analysis of commensal bacteria-induced immunological changes Munakata, Kaori Yamamoto, Masahiro Anjiki, Naoko Nishiyama, Mitsue Imamura, Sachiko Iizuka, Seiichi Takashima, Kiyoe Ishige, Atsushi Hioki, Kyoji Ohnishi, Yasuyuki Watanabe, Kenji BMC Genomics Research Article BACKGROUND: Although microbiota play a critical role in the normal development and function of host immune systems, the underlying mechanisms, especially those involved in the large intestine (LI), remain unknown. In the present study, we performed transcriptome analysis of the LI of germ-free (GF) and specific pathogen-free (SPF) mice of the IQI strain, an inbred strain established from ICR mice. RESULTS: GeneChip analysis, quantitative real-time RT-PCR, and reconfirmation using bacteria-inoculated GF mice revealed differences in the expression levels of several immune-related genes, such as cryptdin-related sequences (CRS), certain subsets of type 1 interferon (IFN)-related genes, class Ib MHC molecules, and certain complements. LI expressed no authentic cryptdins but predominantly expressed CRS2, 4, and 7. The mRNA levels of IFN-related genes, including Irf7, Isgf3g, Ifit1 and Stat1, were lower in SPF- and flora-reconstituted mice. When an oral IFN-α inducer tilorone analog, R11567DA, was administered to SPF mice, IFN-α was induced rapidly in the LI at 4 h, whereas no IFN-α protein was detected in the small intestine (SI) or blood. In situ hybridization and immunohistochemistry suggested that the IFN-α production originated from Paneth cells in the SI, and portions of lamina proprial CD11b- or mPDCA1-positive cells in the LI. CONCLUSION: The present study suggests that microbial colonization, while inducing the expression of anti-microbial peptides, results in the down-regulation of certain genes responsible for immune responses, especially for type I IFN synthesis. This may reflect the adaptation process of the immune system in the LI to prevent excessive inflammation with respect to continuous microbial exposure. Further, the repertoire of anti-microbial peptides and the extraordinary role of interferon producing cells in the LI have been found to be distinct from those in the SI. BioMed Central 2008-04-26 /pmc/articles/PMC2408602/ /pubmed/18439305 http://dx.doi.org/10.1186/1471-2164-9-192 Text en Copyright © 2008 Munakata et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Munakata, Kaori Yamamoto, Masahiro Anjiki, Naoko Nishiyama, Mitsue Imamura, Sachiko Iizuka, Seiichi Takashima, Kiyoe Ishige, Atsushi Hioki, Kyoji Ohnishi, Yasuyuki Watanabe, Kenji Importance of the interferon-α system in murine large intestine indicated by microarray analysis of commensal bacteria-induced immunological changes |
title | Importance of the interferon-α system in murine large intestine indicated by microarray analysis of commensal bacteria-induced immunological changes |
title_full | Importance of the interferon-α system in murine large intestine indicated by microarray analysis of commensal bacteria-induced immunological changes |
title_fullStr | Importance of the interferon-α system in murine large intestine indicated by microarray analysis of commensal bacteria-induced immunological changes |
title_full_unstemmed | Importance of the interferon-α system in murine large intestine indicated by microarray analysis of commensal bacteria-induced immunological changes |
title_short | Importance of the interferon-α system in murine large intestine indicated by microarray analysis of commensal bacteria-induced immunological changes |
title_sort | importance of the interferon-α system in murine large intestine indicated by microarray analysis of commensal bacteria-induced immunological changes |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2408602/ https://www.ncbi.nlm.nih.gov/pubmed/18439305 http://dx.doi.org/10.1186/1471-2164-9-192 |
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