Fish gut-liver immunity during homeostasis or inflammation revealed by integrative transcriptome and proteome studies
The gut-associated lymphoid tissue, connected with liver via bile and blood, constructs a local immune environment of both defense and tolerance. The gut-liver immunity has been well-studied in mammals, yet in fish remains largely unknown, even though enteritis as well as liver and gallbladder syndr...
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Veröffentlicht in: | Scientific reports 2016-11, Vol.6 (1), p.36048-36048, Article 36048 |
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creator | Wu, Nan Song, Yu-Long Wang, Bei Zhang, Xiang-Yang Zhang, Xu-Jie Wang, Ya-Li Cheng, Ying-Yin Chen, Dan-Dan Xia, Xiao-Qin Lu, Yi-Shan Zhang, Yong-An |
description | The gut-associated lymphoid tissue, connected with liver
via
bile and blood, constructs a local immune environment of both defense and tolerance. The gut-liver immunity has been well-studied in mammals, yet in fish remains largely unknown, even though enteritis as well as liver and gallbladder syndrome emerged as a limitation in aquaculture. In this study, we performed integrative bioinformatic analysis for both transcriptomic (gut and liver) and proteomic (intestinal mucus and bile) data, in both healthy and infected tilapias. We found more categories of immune transcripts in gut than liver, as well as more adaptive immune in gut meanwhile more innate in liver. Interestingly reduced differential immune transcripts between gut and liver upon inflammation were also revealed. In addition, more immune proteins in bile than intestinal mucus were identified. And bile probably providing immune effectors to intestinal mucus upon inflammation was deduced. Specifically, many key immune transcripts in gut or liver as well as key immune proteins in mucus or bile were demonstrated. Accordingly, we proposed a hypothesized profile of fish gut-liver immunity, during either homeostasis or inflammation. Current data suggested that fish gut and liver may collaborate immunologically while keep homeostasis using own strategies, including potential unique mechanisms. |
doi_str_mv | 10.1038/srep36048 |
format | Article |
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via
bile and blood, constructs a local immune environment of both defense and tolerance. The gut-liver immunity has been well-studied in mammals, yet in fish remains largely unknown, even though enteritis as well as liver and gallbladder syndrome emerged as a limitation in aquaculture. In this study, we performed integrative bioinformatic analysis for both transcriptomic (gut and liver) and proteomic (intestinal mucus and bile) data, in both healthy and infected tilapias. We found more categories of immune transcripts in gut than liver, as well as more adaptive immune in gut meanwhile more innate in liver. Interestingly reduced differential immune transcripts between gut and liver upon inflammation were also revealed. In addition, more immune proteins in bile than intestinal mucus were identified. And bile probably providing immune effectors to intestinal mucus upon inflammation was deduced. Specifically, many key immune transcripts in gut or liver as well as key immune proteins in mucus or bile were demonstrated. Accordingly, we proposed a hypothesized profile of fish gut-liver immunity, during either homeostasis or inflammation. Current data suggested that fish gut and liver may collaborate immunologically while keep homeostasis using own strategies, including potential unique mechanisms.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/srep36048</identifier><identifier>PMID: 27808112</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>38 ; 38/91 ; 631/250/248 ; 631/250/347 ; 82 ; 82/81 ; Aquaculture ; Bile ; Enteritis ; Gallbladder ; Gastrointestinal tract ; Gene expression ; Gut-associated lymphoid tissues ; Homeostasis ; Humanities and Social Sciences ; Immunity ; Immunological tolerance ; Inflammation ; Intestine ; Liver ; Lymphoid tissue ; multidisciplinary ; Proteomics ; Science ; Small intestine</subject><ispartof>Scientific reports, 2016-11, Vol.6 (1), p.36048-36048, Article 36048</ispartof><rights>The Author(s) 2016</rights><rights>Copyright Nature Publishing Group Nov 2016</rights><rights>Copyright © 2016, The Author(s) 2016 The Author(s)</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c438t-cc8717dfadc08a42cfd95c793c1cfd60ad9b4d4cc7df2dba9763037ff5ee7e293</citedby><cites>FETCH-LOGICAL-c438t-cc8717dfadc08a42cfd95c793c1cfd60ad9b4d4cc7df2dba9763037ff5ee7e293</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5093735/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5093735/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,27924,27925,41120,42189,51576,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27808112$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wu, Nan</creatorcontrib><creatorcontrib>Song, Yu-Long</creatorcontrib><creatorcontrib>Wang, Bei</creatorcontrib><creatorcontrib>Zhang, Xiang-Yang</creatorcontrib><creatorcontrib>Zhang, Xu-Jie</creatorcontrib><creatorcontrib>Wang, Ya-Li</creatorcontrib><creatorcontrib>Cheng, Ying-Yin</creatorcontrib><creatorcontrib>Chen, Dan-Dan</creatorcontrib><creatorcontrib>Xia, Xiao-Qin</creatorcontrib><creatorcontrib>Lu, Yi-Shan</creatorcontrib><creatorcontrib>Zhang, Yong-An</creatorcontrib><title>Fish gut-liver immunity during homeostasis or inflammation revealed by integrative transcriptome and proteome studies</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><description>The gut-associated lymphoid tissue, connected with liver
via
bile and blood, constructs a local immune environment of both defense and tolerance. The gut-liver immunity has been well-studied in mammals, yet in fish remains largely unknown, even though enteritis as well as liver and gallbladder syndrome emerged as a limitation in aquaculture. In this study, we performed integrative bioinformatic analysis for both transcriptomic (gut and liver) and proteomic (intestinal mucus and bile) data, in both healthy and infected tilapias. We found more categories of immune transcripts in gut than liver, as well as more adaptive immune in gut meanwhile more innate in liver. Interestingly reduced differential immune transcripts between gut and liver upon inflammation were also revealed. In addition, more immune proteins in bile than intestinal mucus were identified. And bile probably providing immune effectors to intestinal mucus upon inflammation was deduced. Specifically, many key immune transcripts in gut or liver as well as key immune proteins in mucus or bile were demonstrated. Accordingly, we proposed a hypothesized profile of fish gut-liver immunity, during either homeostasis or inflammation. Current data suggested that fish gut and liver may collaborate immunologically while keep homeostasis using own strategies, including potential unique mechanisms.</description><subject>38</subject><subject>38/91</subject><subject>631/250/248</subject><subject>631/250/347</subject><subject>82</subject><subject>82/81</subject><subject>Aquaculture</subject><subject>Bile</subject><subject>Enteritis</subject><subject>Gallbladder</subject><subject>Gastrointestinal tract</subject><subject>Gene expression</subject><subject>Gut-associated lymphoid tissues</subject><subject>Homeostasis</subject><subject>Humanities and Social Sciences</subject><subject>Immunity</subject><subject>Immunological tolerance</subject><subject>Inflammation</subject><subject>Intestine</subject><subject>Liver</subject><subject>Lymphoid tissue</subject><subject>multidisciplinary</subject><subject>Proteomics</subject><subject>Science</subject><subject>Small intestine</subject><issn>2045-2322</issn><issn>2045-2322</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNplkUtrGzEUhUVpaYKbRf9AEXSTBqbVY8YabQIlNA8IdNOuhSzdsRVmpKkeBv_7yjgxbqqNrnS_e3TEQegjJV8p4f23FGHmS9L2b9A5I23XMM7Y25P6DF2k9ETq6phsqXyPzpjoSU8pO0fl1qUNXpfcjG4LEbtpKt7lHbYlOr_GmzBBSFknl3CobT-Mepp0dsHjCFvQI1i82tVGhnWs91vAOWqfTHRzrsNYe4vnGDLsDykX6yB9QO8GPSa4eN4X6Pftj183983jz7uHm--PjWl5nxtjekGFHbQ1pNctM4OVnRGSG1rLJdFWrlrbGlMZZldaiiUnXAxDByCASb5A1wfduawmsAZ89TaqObpJx50K2ql_O95t1DpsVUckF7yrApfPAjH8KZCymlwyMI7aQyhJ0Z4vBectpRX9_Ap9CiX6-r1KScmZ7Aiv1JcDZWJINbrhaIYStc9THfOs7KdT90fyJb0KXB2ANO_Dgnjy5H9qfwFGVa6y</recordid><startdate>20161103</startdate><enddate>20161103</enddate><creator>Wu, Nan</creator><creator>Song, Yu-Long</creator><creator>Wang, Bei</creator><creator>Zhang, Xiang-Yang</creator><creator>Zhang, Xu-Jie</creator><creator>Wang, Ya-Li</creator><creator>Cheng, Ying-Yin</creator><creator>Chen, Dan-Dan</creator><creator>Xia, Xiao-Qin</creator><creator>Lu, Yi-Shan</creator><creator>Zhang, Yong-An</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>C6C</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20161103</creationdate><title>Fish gut-liver immunity during homeostasis or inflammation revealed by integrative transcriptome and proteome studies</title><author>Wu, Nan ; Song, Yu-Long ; Wang, Bei ; Zhang, Xiang-Yang ; Zhang, Xu-Jie ; Wang, Ya-Li ; Cheng, Ying-Yin ; Chen, Dan-Dan ; Xia, Xiao-Qin ; Lu, Yi-Shan ; Zhang, Yong-An</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c438t-cc8717dfadc08a42cfd95c793c1cfd60ad9b4d4cc7df2dba9763037ff5ee7e293</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>38</topic><topic>38/91</topic><topic>631/250/248</topic><topic>631/250/347</topic><topic>82</topic><topic>82/81</topic><topic>Aquaculture</topic><topic>Bile</topic><topic>Enteritis</topic><topic>Gallbladder</topic><topic>Gastrointestinal tract</topic><topic>Gene expression</topic><topic>Gut-associated lymphoid tissues</topic><topic>Homeostasis</topic><topic>Humanities and Social Sciences</topic><topic>Immunity</topic><topic>Immunological tolerance</topic><topic>Inflammation</topic><topic>Intestine</topic><topic>Liver</topic><topic>Lymphoid tissue</topic><topic>multidisciplinary</topic><topic>Proteomics</topic><topic>Science</topic><topic>Small intestine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wu, Nan</creatorcontrib><creatorcontrib>Song, Yu-Long</creatorcontrib><creatorcontrib>Wang, Bei</creatorcontrib><creatorcontrib>Zhang, Xiang-Yang</creatorcontrib><creatorcontrib>Zhang, Xu-Jie</creatorcontrib><creatorcontrib>Wang, Ya-Li</creatorcontrib><creatorcontrib>Cheng, Ying-Yin</creatorcontrib><creatorcontrib>Chen, Dan-Dan</creatorcontrib><creatorcontrib>Xia, Xiao-Qin</creatorcontrib><creatorcontrib>Lu, Yi-Shan</creatorcontrib><creatorcontrib>Zhang, Yong-An</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Scientific reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wu, Nan</au><au>Song, Yu-Long</au><au>Wang, Bei</au><au>Zhang, Xiang-Yang</au><au>Zhang, Xu-Jie</au><au>Wang, Ya-Li</au><au>Cheng, Ying-Yin</au><au>Chen, Dan-Dan</au><au>Xia, Xiao-Qin</au><au>Lu, Yi-Shan</au><au>Zhang, Yong-An</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Fish gut-liver immunity during homeostasis or inflammation revealed by integrative transcriptome and proteome studies</atitle><jtitle>Scientific reports</jtitle><stitle>Sci Rep</stitle><addtitle>Sci Rep</addtitle><date>2016-11-03</date><risdate>2016</risdate><volume>6</volume><issue>1</issue><spage>36048</spage><epage>36048</epage><pages>36048-36048</pages><artnum>36048</artnum><issn>2045-2322</issn><eissn>2045-2322</eissn><abstract>The gut-associated lymphoid tissue, connected with liver
via
bile and blood, constructs a local immune environment of both defense and tolerance. The gut-liver immunity has been well-studied in mammals, yet in fish remains largely unknown, even though enteritis as well as liver and gallbladder syndrome emerged as a limitation in aquaculture. In this study, we performed integrative bioinformatic analysis for both transcriptomic (gut and liver) and proteomic (intestinal mucus and bile) data, in both healthy and infected tilapias. We found more categories of immune transcripts in gut than liver, as well as more adaptive immune in gut meanwhile more innate in liver. Interestingly reduced differential immune transcripts between gut and liver upon inflammation were also revealed. In addition, more immune proteins in bile than intestinal mucus were identified. And bile probably providing immune effectors to intestinal mucus upon inflammation was deduced. Specifically, many key immune transcripts in gut or liver as well as key immune proteins in mucus or bile were demonstrated. Accordingly, we proposed a hypothesized profile of fish gut-liver immunity, during either homeostasis or inflammation. Current data suggested that fish gut and liver may collaborate immunologically while keep homeostasis using own strategies, including potential unique mechanisms.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>27808112</pmid><doi>10.1038/srep36048</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 38 38/91 631/250/248 631/250/347 82 82/81 Aquaculture Bile Enteritis Gallbladder Gastrointestinal tract Gene expression Gut-associated lymphoid tissues Homeostasis Humanities and Social Sciences Immunity Immunological tolerance Inflammation Intestine Liver Lymphoid tissue multidisciplinary Proteomics Science Small intestine |
title | Fish gut-liver immunity during homeostasis or inflammation revealed by integrative transcriptome and proteome studies |
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