REG3γ-deficient mice have altered mucus distribution and increased mucosal inflammatory responses to the microbiota and enteric pathogens in the ileum
REG3γ is considered to have a protective role against infection with Gram-positive bacteria due to its bactericidal activity, but evidence from in vivo studies is lacking. We generated a REG3γ −/− mouse, and investigated the effect of lack of REG3γ on intestinal mucus distribution, spatial compartme...
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Veröffentlicht in: | Mucosal immunology 2014-07, Vol.7 (4), p.939-947 |
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creator | Loonen, L MP Stolte, E H Jaklofsky, M TJ Meijerink, M Dekker, J van Baarlen, P Wells, J M |
description | REG3γ is considered to have a protective role against infection with Gram-positive bacteria due to its bactericidal activity, but evidence from
in vivo
studies is lacking. We generated a REG3γ
−/−
mouse, and investigated the effect of lack of REG3γ on intestinal mucus distribution, spatial compartmentalization of bacteria, and expression of innate immunity genes. Infection studies were also performed with Gram-positive and Gram-negative pathogens to investigate the antimicrobial role of REG3γ. REG3γ
−/−
mice display altered mucus distribution, increased bacterial contact with the epithelium, and elevated inflammatory markers in the ileum without histological evidence of pathology. Infection response pathway genes were differentially expressed in both
Listeria monocytogenes
and
Salmonella enteritidis
infected REG3γ
−/−
and wild-type (wt) mice. Higher amounts of myeloperoxidase and interleukin-22 transcripts were present in the ileal mucosa of REG3γ
−/−
than wt mice, but translocation to the organs was unaffected. We concluded that REG3γ has a protective role against mucosal infection with pathogenic
Listeria
and
Salmonella in vivo
. REG3γ is equally distributed throughout the mucus and its absence results in increased epithelial contact with the microbiota resulting in low-grade inflammation. REG3γ can bind to Gram-negative and Gram-positive bacteria and influence mucus distribution in the ileum, properties which may contribute to mucosal protection. |
doi_str_mv | 10.1038/mi.2013.109 |
format | Article |
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in vivo
studies is lacking. We generated a REG3γ
−/−
mouse, and investigated the effect of lack of REG3γ on intestinal mucus distribution, spatial compartmentalization of bacteria, and expression of innate immunity genes. Infection studies were also performed with Gram-positive and Gram-negative pathogens to investigate the antimicrobial role of REG3γ. REG3γ
−/−
mice display altered mucus distribution, increased bacterial contact with the epithelium, and elevated inflammatory markers in the ileum without histological evidence of pathology. Infection response pathway genes were differentially expressed in both
Listeria monocytogenes
and
Salmonella enteritidis
infected REG3γ
−/−
and wild-type (wt) mice. Higher amounts of myeloperoxidase and interleukin-22 transcripts were present in the ileal mucosa of REG3γ
−/−
than wt mice, but translocation to the organs was unaffected. We concluded that REG3γ has a protective role against mucosal infection with pathogenic
Listeria
and
Salmonella in vivo
. REG3γ is equally distributed throughout the mucus and its absence results in increased epithelial contact with the microbiota resulting in low-grade inflammation. REG3γ can bind to Gram-negative and Gram-positive bacteria and influence mucus distribution in the ileum, properties which may contribute to mucosal protection.</description><identifier>ISSN: 1933-0219</identifier><identifier>EISSN: 1935-3456</identifier><identifier>DOI: 10.1038/mi.2013.109</identifier><identifier>PMID: 24345802</identifier><language>eng</language><publisher>New York: Nature Publishing Group US</publisher><subject>631/250/256 ; 631/250/347 ; 631/326/41/2533 ; 692/698/2741/2135 ; Allergology ; Animals ; Antibodies ; Biomedical and Life Sciences ; Biomedicine ; Disease Models, Animal ; Gastroenterology ; Gene Expression Profiling ; Ileum - immunology ; Ileum - metabolism ; Ileum - microbiology ; Immunity, Innate ; Immunology ; Inflammation - genetics ; Inflammation - immunology ; Inflammation - microbiology ; Interferon Regulatory Factors - metabolism ; Interferons - metabolism ; Interleukin-1beta - metabolism ; Intestinal Mucosa - immunology ; Intestinal Mucosa - metabolism ; Intestinal Mucosa - microbiology ; Listeria monocytogenes - physiology ; Mice ; Mice, Knockout ; Microbiota ; Mucus - metabolism ; Myeloid Differentiation Factor 88 - metabolism ; Pancreatitis-Associated Proteins ; Proteins - genetics ; Salmonella enteritidis - physiology ; Signal Transduction ; STAT1 Transcription Factor - metabolism ; STAT3 Transcription Factor - metabolism ; Toll-Like Receptor 3 - metabolism</subject><ispartof>Mucosal immunology, 2014-07, Vol.7 (4), p.939-947</ispartof><rights>Society for Mucosal Immunology 2014</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c363t-8c07155bdf439c06b436ef495f31f679a64b5ac17f1adb8a6d3953d1f488c7a23</citedby><cites>FETCH-LOGICAL-c363t-8c07155bdf439c06b436ef495f31f679a64b5ac17f1adb8a6d3953d1f488c7a23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24345802$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Loonen, L MP</creatorcontrib><creatorcontrib>Stolte, E H</creatorcontrib><creatorcontrib>Jaklofsky, M TJ</creatorcontrib><creatorcontrib>Meijerink, M</creatorcontrib><creatorcontrib>Dekker, J</creatorcontrib><creatorcontrib>van Baarlen, P</creatorcontrib><creatorcontrib>Wells, J M</creatorcontrib><title>REG3γ-deficient mice have altered mucus distribution and increased mucosal inflammatory responses to the microbiota and enteric pathogens in the ileum</title><title>Mucosal immunology</title><addtitle>Mucosal Immunol</addtitle><addtitle>Mucosal Immunol</addtitle><description>REG3γ is considered to have a protective role against infection with Gram-positive bacteria due to its bactericidal activity, but evidence from
in vivo
studies is lacking. We generated a REG3γ
−/−
mouse, and investigated the effect of lack of REG3γ on intestinal mucus distribution, spatial compartmentalization of bacteria, and expression of innate immunity genes. Infection studies were also performed with Gram-positive and Gram-negative pathogens to investigate the antimicrobial role of REG3γ. REG3γ
−/−
mice display altered mucus distribution, increased bacterial contact with the epithelium, and elevated inflammatory markers in the ileum without histological evidence of pathology. Infection response pathway genes were differentially expressed in both
Listeria monocytogenes
and
Salmonella enteritidis
infected REG3γ
−/−
and wild-type (wt) mice. Higher amounts of myeloperoxidase and interleukin-22 transcripts were present in the ileal mucosa of REG3γ
−/−
than wt mice, but translocation to the organs was unaffected. We concluded that REG3γ has a protective role against mucosal infection with pathogenic
Listeria
and
Salmonella in vivo
. REG3γ is equally distributed throughout the mucus and its absence results in increased epithelial contact with the microbiota resulting in low-grade inflammation. REG3γ can bind to Gram-negative and Gram-positive bacteria and influence mucus distribution in the ileum, properties which may contribute to mucosal protection.</description><subject>631/250/256</subject><subject>631/250/347</subject><subject>631/326/41/2533</subject><subject>692/698/2741/2135</subject><subject>Allergology</subject><subject>Animals</subject><subject>Antibodies</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Disease Models, Animal</subject><subject>Gastroenterology</subject><subject>Gene Expression Profiling</subject><subject>Ileum - immunology</subject><subject>Ileum - metabolism</subject><subject>Ileum - microbiology</subject><subject>Immunity, Innate</subject><subject>Immunology</subject><subject>Inflammation - genetics</subject><subject>Inflammation - immunology</subject><subject>Inflammation - microbiology</subject><subject>Interferon Regulatory Factors - metabolism</subject><subject>Interferons - metabolism</subject><subject>Interleukin-1beta - metabolism</subject><subject>Intestinal Mucosa - immunology</subject><subject>Intestinal Mucosa - metabolism</subject><subject>Intestinal Mucosa - microbiology</subject><subject>Listeria monocytogenes - physiology</subject><subject>Mice</subject><subject>Mice, Knockout</subject><subject>Microbiota</subject><subject>Mucus - metabolism</subject><subject>Myeloid Differentiation Factor 88 - metabolism</subject><subject>Pancreatitis-Associated Proteins</subject><subject>Proteins - genetics</subject><subject>Salmonella enteritidis - physiology</subject><subject>Signal Transduction</subject><subject>STAT1 Transcription Factor - metabolism</subject><subject>STAT3 Transcription Factor - metabolism</subject><subject>Toll-Like Receptor 3 - metabolism</subject><issn>1933-0219</issn><issn>1935-3456</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNptkc9OHSEUxknTplp15d6wbNKOwjDMn6UxVpuYNDG6npyBgxczwBWYJj6JD9L38JnKvde66grO4fd9Jx-HkGPOTjkT_ZmzpzXjohTDB7LPByEr0cj24_YuKlbzYY98SemRsZYxKT6TvbopRM_qffJye3klXv9UGo1VFn2mziqkK_iNFOaMETV1i1oS1TblaKcl2-ApeE2tVxEh7YCQYC4dM4NzkEN8phHTOviEieZA8wo3xjFMNmTYysssjFbRNeRVeECfinzL2RkXd0g-GZgTHr2dB-T-x-XdxXV18-vq58X5TaVEK3LVK9ZxKSdtGjEo1k6NaNE0gzSCm7YboG0mCYp3hoOeemi1GKTQ3DR9rzqoxQH5uvNdx_C0YMqjs0nhPIPHsKSRS9HxXnY9K-i3HVpipBTRjOtoHcTnkbNxs4kiHTebKMVQ6JM342VyqN_Zf19fgO87IJUn_4BxfAxL9CXsf_3-AvYPliE</recordid><startdate>20140701</startdate><enddate>20140701</enddate><creator>Loonen, L MP</creator><creator>Stolte, E H</creator><creator>Jaklofsky, M TJ</creator><creator>Meijerink, M</creator><creator>Dekker, J</creator><creator>van Baarlen, P</creator><creator>Wells, J M</creator><general>Nature Publishing Group US</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20140701</creationdate><title>REG3γ-deficient mice have altered mucus distribution and increased mucosal inflammatory responses to the microbiota and enteric pathogens in the ileum</title><author>Loonen, L MP ; Stolte, E H ; Jaklofsky, M TJ ; Meijerink, M ; Dekker, J ; van Baarlen, P ; Wells, J M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c363t-8c07155bdf439c06b436ef495f31f679a64b5ac17f1adb8a6d3953d1f488c7a23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>631/250/256</topic><topic>631/250/347</topic><topic>631/326/41/2533</topic><topic>692/698/2741/2135</topic><topic>Allergology</topic><topic>Animals</topic><topic>Antibodies</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Disease Models, Animal</topic><topic>Gastroenterology</topic><topic>Gene Expression Profiling</topic><topic>Ileum - immunology</topic><topic>Ileum - metabolism</topic><topic>Ileum - microbiology</topic><topic>Immunity, Innate</topic><topic>Immunology</topic><topic>Inflammation - genetics</topic><topic>Inflammation - immunology</topic><topic>Inflammation - microbiology</topic><topic>Interferon Regulatory Factors - metabolism</topic><topic>Interferons - metabolism</topic><topic>Interleukin-1beta - metabolism</topic><topic>Intestinal Mucosa - immunology</topic><topic>Intestinal Mucosa - metabolism</topic><topic>Intestinal Mucosa - microbiology</topic><topic>Listeria monocytogenes - physiology</topic><topic>Mice</topic><topic>Mice, Knockout</topic><topic>Microbiota</topic><topic>Mucus - metabolism</topic><topic>Myeloid Differentiation Factor 88 - metabolism</topic><topic>Pancreatitis-Associated Proteins</topic><topic>Proteins - genetics</topic><topic>Salmonella enteritidis - physiology</topic><topic>Signal Transduction</topic><topic>STAT1 Transcription Factor - metabolism</topic><topic>STAT3 Transcription Factor - metabolism</topic><topic>Toll-Like Receptor 3 - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Loonen, L MP</creatorcontrib><creatorcontrib>Stolte, E H</creatorcontrib><creatorcontrib>Jaklofsky, M TJ</creatorcontrib><creatorcontrib>Meijerink, M</creatorcontrib><creatorcontrib>Dekker, J</creatorcontrib><creatorcontrib>van Baarlen, P</creatorcontrib><creatorcontrib>Wells, J M</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Mucosal immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Loonen, L MP</au><au>Stolte, E H</au><au>Jaklofsky, M TJ</au><au>Meijerink, M</au><au>Dekker, J</au><au>van Baarlen, P</au><au>Wells, J M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>REG3γ-deficient mice have altered mucus distribution and increased mucosal inflammatory responses to the microbiota and enteric pathogens in the ileum</atitle><jtitle>Mucosal immunology</jtitle><stitle>Mucosal Immunol</stitle><addtitle>Mucosal Immunol</addtitle><date>2014-07-01</date><risdate>2014</risdate><volume>7</volume><issue>4</issue><spage>939</spage><epage>947</epage><pages>939-947</pages><issn>1933-0219</issn><eissn>1935-3456</eissn><abstract>REG3γ is considered to have a protective role against infection with Gram-positive bacteria due to its bactericidal activity, but evidence from
in vivo
studies is lacking. We generated a REG3γ
−/−
mouse, and investigated the effect of lack of REG3γ on intestinal mucus distribution, spatial compartmentalization of bacteria, and expression of innate immunity genes. Infection studies were also performed with Gram-positive and Gram-negative pathogens to investigate the antimicrobial role of REG3γ. REG3γ
−/−
mice display altered mucus distribution, increased bacterial contact with the epithelium, and elevated inflammatory markers in the ileum without histological evidence of pathology. Infection response pathway genes were differentially expressed in both
Listeria monocytogenes
and
Salmonella enteritidis
infected REG3γ
−/−
and wild-type (wt) mice. Higher amounts of myeloperoxidase and interleukin-22 transcripts were present in the ileal mucosa of REG3γ
−/−
than wt mice, but translocation to the organs was unaffected. We concluded that REG3γ has a protective role against mucosal infection with pathogenic
Listeria
and
Salmonella in vivo
. REG3γ is equally distributed throughout the mucus and its absence results in increased epithelial contact with the microbiota resulting in low-grade inflammation. REG3γ can bind to Gram-negative and Gram-positive bacteria and influence mucus distribution in the ileum, properties which may contribute to mucosal protection.</abstract><cop>New York</cop><pub>Nature Publishing Group US</pub><pmid>24345802</pmid><doi>10.1038/mi.2013.109</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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ispartof | Mucosal immunology, 2014-07, Vol.7 (4), p.939-947 |
issn | 1933-0219 1935-3456 |
language | eng |
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source | MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection |
subjects | 631/250/256 631/250/347 631/326/41/2533 692/698/2741/2135 Allergology Animals Antibodies Biomedical and Life Sciences Biomedicine Disease Models, Animal Gastroenterology Gene Expression Profiling Ileum - immunology Ileum - metabolism Ileum - microbiology Immunity, Innate Immunology Inflammation - genetics Inflammation - immunology Inflammation - microbiology Interferon Regulatory Factors - metabolism Interferons - metabolism Interleukin-1beta - metabolism Intestinal Mucosa - immunology Intestinal Mucosa - metabolism Intestinal Mucosa - microbiology Listeria monocytogenes - physiology Mice Mice, Knockout Microbiota Mucus - metabolism Myeloid Differentiation Factor 88 - metabolism Pancreatitis-Associated Proteins Proteins - genetics Salmonella enteritidis - physiology Signal Transduction STAT1 Transcription Factor - metabolism STAT3 Transcription Factor - metabolism Toll-Like Receptor 3 - metabolism |
title | REG3γ-deficient mice have altered mucus distribution and increased mucosal inflammatory responses to the microbiota and enteric pathogens in the ileum |
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