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Soluble CEACAM8 interacts with CEACAM1 inhibiting TLR2-triggered immune responses
Lower respiratory tract bacterial infections are characterized by neutrophilic inflammation in the airways. The carcinoembryonic antigen-related cell adhesion molecule (CEACAM) 8 is expressed in and released by human granulocytes. Our study demonstrates that human granulocytes release CEACAM8 in res...
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Published in: | PloS one 2014-04, Vol.9 (4), p.e94106-e94106 |
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creator | Singer, Bernhard B Opp, Lena Heinrich, Annina Schreiber, Frauke Binding-Liermann, Ramona Berrocal-Almanza, Luis Carlos Heyl, Kerstin A Müller, Mario M Weimann, Andreas Zweigner, Janine Slevogt, Hortense |
description | Lower respiratory tract bacterial infections are characterized by neutrophilic inflammation in the airways. The carcinoembryonic antigen-related cell adhesion molecule (CEACAM) 8 is expressed in and released by human granulocytes. Our study demonstrates that human granulocytes release CEACAM8 in response to bacterial DNA in a TLR9-dependent manner. Individuals with a high percentage of bronchial lavage fluid (BALF) granulocytes were more likely to have detectable levels of released CEACAM8 in the BALF than those with a normal granulocyte count. Soluble, recombinant CEACAM8-Fc binds to CEACAM1 expressed on human airway epithelium. Application of CEACAM8-Fc to CEACAM1-positive human pulmonary epithelial cells resulted in reduced TLR2-dependent inflammatory responses. These inhibitory effects were accompanied by tyrosine phosphorylation of the immunoreceptor tyrosine-based inhibitory motif (ITIM) of CEACAM1 and by recruitment of the phosphatase SHP-1, which could negatively regulate Toll-like receptor 2-dependent activation of the phosphatidylinositol 3-OH kinase-Akt kinase pathway. Our results suggest a new mechanism by which granulocytes reduce pro-inflammatory immune responses in human airways via secretion of CEACAM8 in neutrophil-driven bacterial infections. |
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The carcinoembryonic antigen-related cell adhesion molecule (CEACAM) 8 is expressed in and released by human granulocytes. Our study demonstrates that human granulocytes release CEACAM8 in response to bacterial DNA in a TLR9-dependent manner. Individuals with a high percentage of bronchial lavage fluid (BALF) granulocytes were more likely to have detectable levels of released CEACAM8 in the BALF than those with a normal granulocyte count. Soluble, recombinant CEACAM8-Fc binds to CEACAM1 expressed on human airway epithelium. Application of CEACAM8-Fc to CEACAM1-positive human pulmonary epithelial cells resulted in reduced TLR2-dependent inflammatory responses. These inhibitory effects were accompanied by tyrosine phosphorylation of the immunoreceptor tyrosine-based inhibitory motif (ITIM) of CEACAM1 and by recruitment of the phosphatase SHP-1, which could negatively regulate Toll-like receptor 2-dependent activation of the phosphatidylinositol 3-OH kinase-Akt kinase pathway. Our results suggest a new mechanism by which granulocytes reduce pro-inflammatory immune responses in human airways via secretion of CEACAM8 in neutrophil-driven bacterial infections.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0094106</identifier><identifier>PMID: 24743304</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>AKT protein ; Analysis ; Animals ; Antigens ; Antigens, CD - chemistry ; Antigens, CD - metabolism ; Bacteria ; Bacterial infections ; Biology and Life Sciences ; Bronchi - cytology ; Bronchi - immunology ; Bronchoalveolar Lavage Fluid ; Carcinoembryonic antigen ; Care and treatment ; CD66 antigen ; CEACAM1 protein ; Cell adhesion ; Cell adhesion & migration ; Cell adhesion molecules ; Cell Adhesion Molecules - chemistry ; Cell Adhesion Molecules - metabolism ; Cell Count ; Cell Line ; Chemokines ; Cytochalasin D - pharmacology ; Deoxyribonucleic acid ; DNA ; Epithelial cells ; Epithelial Cells - cytology ; Epithelial Cells - drug effects ; Epithelial Cells - metabolism ; Epithelium ; GPI-Linked Proteins - chemistry ; GPI-Linked Proteins - metabolism ; Granulocytes ; Granulocytes - cytology ; Granulocytes - drug effects ; Health aspects ; Hospitals ; Hostages ; Human behavior ; Humans ; Hygiene ; Immune response ; Immune system ; Immunoglobulins ; Immunology ; Immunoreceptor tyrosine-based inhibition motif ; Infections ; Inflammation ; Kinases ; Laboratories ; Leukocytes (granulocytic) ; Leukocytes (neutrophilic) ; Medicine and Health Sciences ; Moraxella catarrhalis ; Neutrophils ; Phosphorylation ; Physical Sciences ; Protein Binding ; Proteins ; Rats ; Recruitment ; Respiratory tract ; Respiratory tract diseases ; SHP-1 protein ; Signal Transduction - drug effects ; Solubility ; TLR2 protein ; TLR9 protein ; Toll-Like Receptor 2 - metabolism ; Toll-Like Receptor 9 - metabolism ; Toll-like receptors ; Tyrosine</subject><ispartof>PloS one, 2014-04, Vol.9 (4), p.e94106-e94106</ispartof><rights>COPYRIGHT 2014 Public Library of Science</rights><rights>2014 Singer et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2014 Singer et al 2014 Singer et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c692t-bc5f70d3022c980e9b80818fe151f54b1b8cfa05cc31751d104e0799580b67213</citedby><cites>FETCH-LOGICAL-c692t-bc5f70d3022c980e9b80818fe151f54b1b8cfa05cc31751d104e0799580b67213</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1518902315/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1518902315?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,724,777,781,882,25734,27905,27906,36993,36994,44571,53772,53774,74875</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24743304$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Tran, Dat Quoc</contributor><creatorcontrib>Singer, Bernhard B</creatorcontrib><creatorcontrib>Opp, Lena</creatorcontrib><creatorcontrib>Heinrich, Annina</creatorcontrib><creatorcontrib>Schreiber, Frauke</creatorcontrib><creatorcontrib>Binding-Liermann, Ramona</creatorcontrib><creatorcontrib>Berrocal-Almanza, Luis Carlos</creatorcontrib><creatorcontrib>Heyl, Kerstin A</creatorcontrib><creatorcontrib>Müller, Mario M</creatorcontrib><creatorcontrib>Weimann, Andreas</creatorcontrib><creatorcontrib>Zweigner, Janine</creatorcontrib><creatorcontrib>Slevogt, Hortense</creatorcontrib><title>Soluble CEACAM8 interacts with CEACAM1 inhibiting TLR2-triggered immune responses</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Lower respiratory tract bacterial infections are characterized by neutrophilic inflammation in the airways. The carcinoembryonic antigen-related cell adhesion molecule (CEACAM) 8 is expressed in and released by human granulocytes. Our study demonstrates that human granulocytes release CEACAM8 in response to bacterial DNA in a TLR9-dependent manner. Individuals with a high percentage of bronchial lavage fluid (BALF) granulocytes were more likely to have detectable levels of released CEACAM8 in the BALF than those with a normal granulocyte count. Soluble, recombinant CEACAM8-Fc binds to CEACAM1 expressed on human airway epithelium. Application of CEACAM8-Fc to CEACAM1-positive human pulmonary epithelial cells resulted in reduced TLR2-dependent inflammatory responses. These inhibitory effects were accompanied by tyrosine phosphorylation of the immunoreceptor tyrosine-based inhibitory motif (ITIM) of CEACAM1 and by recruitment of the phosphatase SHP-1, which could negatively regulate Toll-like receptor 2-dependent activation of the phosphatidylinositol 3-OH kinase-Akt kinase pathway. Our results suggest a new mechanism by which granulocytes reduce pro-inflammatory immune responses in human airways via secretion of CEACAM8 in neutrophil-driven bacterial infections.</description><subject>AKT protein</subject><subject>Analysis</subject><subject>Animals</subject><subject>Antigens</subject><subject>Antigens, CD - chemistry</subject><subject>Antigens, CD - metabolism</subject><subject>Bacteria</subject><subject>Bacterial infections</subject><subject>Biology and Life Sciences</subject><subject>Bronchi - cytology</subject><subject>Bronchi - immunology</subject><subject>Bronchoalveolar Lavage Fluid</subject><subject>Carcinoembryonic antigen</subject><subject>Care and treatment</subject><subject>CD66 antigen</subject><subject>CEACAM1 protein</subject><subject>Cell adhesion</subject><subject>Cell adhesion & migration</subject><subject>Cell adhesion molecules</subject><subject>Cell Adhesion Molecules - chemistry</subject><subject>Cell Adhesion Molecules - metabolism</subject><subject>Cell Count</subject><subject>Cell Line</subject><subject>Chemokines</subject><subject>Cytochalasin D - pharmacology</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>Epithelial cells</subject><subject>Epithelial Cells - cytology</subject><subject>Epithelial Cells - drug effects</subject><subject>Epithelial Cells - metabolism</subject><subject>Epithelium</subject><subject>GPI-Linked Proteins - chemistry</subject><subject>GPI-Linked Proteins - metabolism</subject><subject>Granulocytes</subject><subject>Granulocytes - cytology</subject><subject>Granulocytes - drug effects</subject><subject>Health aspects</subject><subject>Hospitals</subject><subject>Hostages</subject><subject>Human behavior</subject><subject>Humans</subject><subject>Hygiene</subject><subject>Immune response</subject><subject>Immune system</subject><subject>Immunoglobulins</subject><subject>Immunology</subject><subject>Immunoreceptor tyrosine-based inhibition motif</subject><subject>Infections</subject><subject>Inflammation</subject><subject>Kinases</subject><subject>Laboratories</subject><subject>Leukocytes (granulocytic)</subject><subject>Leukocytes (neutrophilic)</subject><subject>Medicine and Health Sciences</subject><subject>Moraxella catarrhalis</subject><subject>Neutrophils</subject><subject>Phosphorylation</subject><subject>Physical Sciences</subject><subject>Protein Binding</subject><subject>Proteins</subject><subject>Rats</subject><subject>Recruitment</subject><subject>Respiratory tract</subject><subject>Respiratory tract diseases</subject><subject>SHP-1 protein</subject><subject>Signal Transduction - drug effects</subject><subject>Solubility</subject><subject>TLR2 protein</subject><subject>TLR9 protein</subject><subject>Toll-Like Receptor 2 - metabolism</subject><subject>Toll-Like Receptor 9 - metabolism</subject><subject>Toll-like receptors</subject><subject>Tyrosine</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqNkl1v0zAUhiMEYmPwDxBEQkJw0eKPOLFvkKpqQKWiiW1waznOSeoqiTvb4ePf467Z1KBdoFwkOn7e9xyfvEnyEqM5pgX-sLWD61U739ke5giJDKP8UXKKBSWznCD6-Oj7JHnm_RYhRnmeP01OSFZklKLsNPl2ZduhbCFdni-Wi688NX0Ap3Tw6S8TNmMZx_LGlCaYvkmv15dkFpxpGnBQpabrhh5SBz5O4sE_T57UqvXwYnyfJd8_nV8vv8zWF59Xy8V6pnNBwqzUrC5QRREhWnAEouSIY14DZrhmWYlLrmuFmNYUFwxXGGWACiEYR2VeEEzPktcH311rvRy34WWUc4EIxSwSqwNRWbWVO2c65f5Iq4y8LVjXSOWC0S1IneVFkXFK4oayqC8rpCggpjiqKRM0en0cuw1lB5WGPjjVTkynJ73ZyMb-lFQIxEgeDd6NBs7eDOCD7IzX0LaqBzvczl1wjgjbz_3mH_Th241Uo-IFTF_b2FfvTeWCFoxxSum-7fwBKj4VdEbH6NQm1ieC9xNBZAL8Do0avJerq8v_Zy9-TNm3R-wGVBs2PmYvmJiaKZgdQO2s9w7q-yVjJPfJv9uG3CdfjsmPslfHP-hedBd1-hf0APnJ</recordid><startdate>20140401</startdate><enddate>20140401</enddate><creator>Singer, Bernhard B</creator><creator>Opp, Lena</creator><creator>Heinrich, Annina</creator><creator>Schreiber, Frauke</creator><creator>Binding-Liermann, Ramona</creator><creator>Berrocal-Almanza, Luis Carlos</creator><creator>Heyl, Kerstin A</creator><creator>Müller, Mario M</creator><creator>Weimann, Andreas</creator><creator>Zweigner, Janine</creator><creator>Slevogt, Hortense</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</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>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20140401</creationdate><title>Soluble CEACAM8 interacts with CEACAM1 inhibiting TLR2-triggered immune responses</title><author>Singer, Bernhard B ; Opp, Lena ; Heinrich, Annina ; Schreiber, Frauke ; Binding-Liermann, Ramona ; Berrocal-Almanza, Luis Carlos ; Heyl, Kerstin A ; Müller, Mario M ; Weimann, Andreas ; Zweigner, Janine ; Slevogt, Hortense</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c692t-bc5f70d3022c980e9b80818fe151f54b1b8cfa05cc31751d104e0799580b67213</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>AKT protein</topic><topic>Analysis</topic><topic>Animals</topic><topic>Antigens</topic><topic>Antigens, CD - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Singer, Bernhard B</au><au>Opp, Lena</au><au>Heinrich, Annina</au><au>Schreiber, Frauke</au><au>Binding-Liermann, Ramona</au><au>Berrocal-Almanza, Luis Carlos</au><au>Heyl, Kerstin A</au><au>Müller, Mario M</au><au>Weimann, Andreas</au><au>Zweigner, Janine</au><au>Slevogt, Hortense</au><au>Tran, Dat Quoc</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Soluble CEACAM8 interacts with CEACAM1 inhibiting TLR2-triggered immune responses</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2014-04-01</date><risdate>2014</risdate><volume>9</volume><issue>4</issue><spage>e94106</spage><epage>e94106</epage><pages>e94106-e94106</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Lower respiratory tract bacterial infections are characterized by neutrophilic inflammation in the airways. The carcinoembryonic antigen-related cell adhesion molecule (CEACAM) 8 is expressed in and released by human granulocytes. Our study demonstrates that human granulocytes release CEACAM8 in response to bacterial DNA in a TLR9-dependent manner. Individuals with a high percentage of bronchial lavage fluid (BALF) granulocytes were more likely to have detectable levels of released CEACAM8 in the BALF than those with a normal granulocyte count. Soluble, recombinant CEACAM8-Fc binds to CEACAM1 expressed on human airway epithelium. Application of CEACAM8-Fc to CEACAM1-positive human pulmonary epithelial cells resulted in reduced TLR2-dependent inflammatory responses. These inhibitory effects were accompanied by tyrosine phosphorylation of the immunoreceptor tyrosine-based inhibitory motif (ITIM) of CEACAM1 and by recruitment of the phosphatase SHP-1, which could negatively regulate Toll-like receptor 2-dependent activation of the phosphatidylinositol 3-OH kinase-Akt kinase pathway. Our results suggest a new mechanism by which granulocytes reduce pro-inflammatory immune responses in human airways via secretion of CEACAM8 in neutrophil-driven bacterial infections.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>24743304</pmid><doi>10.1371/journal.pone.0094106</doi><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1932-6203 |
ispartof | PloS one, 2014-04, Vol.9 (4), p.e94106-e94106 |
issn | 1932-6203 1932-6203 |
language | eng |
recordid | cdi_plos_journals_1518902315 |
source | Publicly Available Content (ProQuest); PubMed Central |
subjects | AKT protein Analysis Animals Antigens Antigens, CD - chemistry Antigens, CD - metabolism Bacteria Bacterial infections Biology and Life Sciences Bronchi - cytology Bronchi - immunology Bronchoalveolar Lavage Fluid Carcinoembryonic antigen Care and treatment CD66 antigen CEACAM1 protein Cell adhesion Cell adhesion & migration Cell adhesion molecules Cell Adhesion Molecules - chemistry Cell Adhesion Molecules - metabolism Cell Count Cell Line Chemokines Cytochalasin D - pharmacology Deoxyribonucleic acid DNA Epithelial cells Epithelial Cells - cytology Epithelial Cells - drug effects Epithelial Cells - metabolism Epithelium GPI-Linked Proteins - chemistry GPI-Linked Proteins - metabolism Granulocytes Granulocytes - cytology Granulocytes - drug effects Health aspects Hospitals Hostages Human behavior Humans Hygiene Immune response Immune system Immunoglobulins Immunology Immunoreceptor tyrosine-based inhibition motif Infections Inflammation Kinases Laboratories Leukocytes (granulocytic) Leukocytes (neutrophilic) Medicine and Health Sciences Moraxella catarrhalis Neutrophils Phosphorylation Physical Sciences Protein Binding Proteins Rats Recruitment Respiratory tract Respiratory tract diseases SHP-1 protein Signal Transduction - drug effects Solubility TLR2 protein TLR9 protein Toll-Like Receptor 2 - metabolism Toll-Like Receptor 9 - metabolism Toll-like receptors Tyrosine |
title | Soluble CEACAM8 interacts with CEACAM1 inhibiting TLR2-triggered immune responses |
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