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Comparative analysis of Annexin A1-formyl peptide receptor 2/ALX expression in human leukocyte subsets
Recent studies have associated the dysregulated expression of Annexin-A1/Formyl peptide receptor 2 (FPR2/ALX) system with the development of autoimmune diseases. In this study we systematically scanned human leukocyte subsets for the presence of this pathway aiming to provide a roadmap that will hel...
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Published in: | International immunopharmacology 2011, Vol.11 (1), p.55-66 |
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description | Recent studies have associated the dysregulated expression of Annexin-A1/Formyl peptide receptor 2 (FPR2/ALX) system with the development of autoimmune diseases. In this study we systematically scanned human leukocyte subsets for the presence of this pathway aiming to provide a roadmap that will help investigators to explore possible links between the development of immune related disorders and the expression of this system. Our results show that neutrophils, monocytes and NK cells express higher levels of both AnxA1 and FPR2/ALX compared to T or B cells. Further analysis of specific T cell subsets revealed higher levels in activated CD25
+ and memory CD45RO CD4 T cells compared to resting CD25
− or naïve CD45RA CD4 T cells. Together the results expand our knowledge of the AnxA1-FPR2/ALX system in immune cells and provide new avenues for investigation into the functions of this signalling pathway in systems other than that classically described for neutrophils.
►This is the first study showing FPR2/ALX as the genuine receptor for full-length Annexin-A1. ►This study demonstrated that Annexin-A1 modulates the strength of TCR signalling. ►A comprehensive review of the biological functions of formyl peptide receptors. ►This study provided the first evidence of Annexin-A1-derived peptides as ligand for formyl peptide receptors. |
doi_str_mv | 10.1016/j.intimp.2010.10.006 |
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+ and memory CD45RO CD4 T cells compared to resting CD25
− or naïve CD45RA CD4 T cells. Together the results expand our knowledge of the AnxA1-FPR2/ALX system in immune cells and provide new avenues for investigation into the functions of this signalling pathway in systems other than that classically described for neutrophils.
►This is the first study showing FPR2/ALX as the genuine receptor for full-length Annexin-A1. ►This study demonstrated that Annexin-A1 modulates the strength of TCR signalling. ►A comprehensive review of the biological functions of formyl peptide receptors. ►This study provided the first evidence of Annexin-A1-derived peptides as ligand for formyl peptide receptors.</description><identifier>ISSN: 1567-5769</identifier><identifier>EISSN: 1878-1705</identifier><identifier>DOI: 10.1016/j.intimp.2010.10.006</identifier><identifier>PMID: 20974309</identifier><language>eng</language><publisher>Kidlington: Elsevier B.V</publisher><subject>Adaptive immune cells ; Adult ; Annexin A1 - biosynthesis ; Annexin-A1 ; Autoimmune Diseases - metabolism ; Biological and medical sciences ; Blotting, Western ; Female ; Flow Cytometry ; Formyl peptide receptor 2/ALX ; Humans ; Innate immune cells ; Leukocytes - immunology ; Leukocytes - metabolism ; Leukocytes, Mononuclear - immunology ; Leukocytes, Mononuclear - metabolism ; Male ; Medical sciences ; Neutrophils - immunology ; Neutrophils - metabolism ; Pharmacology. Drug treatments ; Receptors, Formyl Peptide - biosynthesis ; Receptors, Lipoxin - biosynthesis ; T-Lymphocyte Subsets - immunology ; T-Lymphocyte Subsets - metabolism ; Young Adult</subject><ispartof>International immunopharmacology, 2011, Vol.11 (1), p.55-66</ispartof><rights>2010 Elsevier B.V.</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2010 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c489t-c54e3d2fc3377f9e0a76a65d7e734ebf4878fb08df3cb81c65bc21fb2606e5ed3</citedby><cites>FETCH-LOGICAL-c489t-c54e3d2fc3377f9e0a76a65d7e734ebf4878fb08df3cb81c65bc21fb2606e5ed3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4024,27923,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=23768472$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20974309$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Spurr, Lydia</creatorcontrib><creatorcontrib>Nadkarni, Suchita</creatorcontrib><creatorcontrib>Pederzoli-Ribeil, Magali</creatorcontrib><creatorcontrib>Goulding, Nicolas J.</creatorcontrib><creatorcontrib>Perretti, Mauro</creatorcontrib><creatorcontrib>D'Acquisto, Fulvio</creatorcontrib><title>Comparative analysis of Annexin A1-formyl peptide receptor 2/ALX expression in human leukocyte subsets</title><title>International immunopharmacology</title><addtitle>Int Immunopharmacol</addtitle><description>Recent studies have associated the dysregulated expression of Annexin-A1/Formyl peptide receptor 2 (FPR2/ALX) system with the development of autoimmune diseases. In this study we systematically scanned human leukocyte subsets for the presence of this pathway aiming to provide a roadmap that will help investigators to explore possible links between the development of immune related disorders and the expression of this system. Our results show that neutrophils, monocytes and NK cells express higher levels of both AnxA1 and FPR2/ALX compared to T or B cells. Further analysis of specific T cell subsets revealed higher levels in activated CD25
+ and memory CD45RO CD4 T cells compared to resting CD25
− or naïve CD45RA CD4 T cells. Together the results expand our knowledge of the AnxA1-FPR2/ALX system in immune cells and provide new avenues for investigation into the functions of this signalling pathway in systems other than that classically described for neutrophils.
►This is the first study showing FPR2/ALX as the genuine receptor for full-length Annexin-A1. ►This study demonstrated that Annexin-A1 modulates the strength of TCR signalling. ►A comprehensive review of the biological functions of formyl peptide receptors. ►This study provided the first evidence of Annexin-A1-derived peptides as ligand for formyl peptide receptors.</description><subject>Adaptive immune cells</subject><subject>Adult</subject><subject>Annexin A1 - biosynthesis</subject><subject>Annexin-A1</subject><subject>Autoimmune Diseases - metabolism</subject><subject>Biological and medical sciences</subject><subject>Blotting, Western</subject><subject>Female</subject><subject>Flow Cytometry</subject><subject>Formyl peptide receptor 2/ALX</subject><subject>Humans</subject><subject>Innate immune cells</subject><subject>Leukocytes - immunology</subject><subject>Leukocytes - metabolism</subject><subject>Leukocytes, Mononuclear - immunology</subject><subject>Leukocytes, Mononuclear - metabolism</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Neutrophils - immunology</subject><subject>Neutrophils - metabolism</subject><subject>Pharmacology. Drug treatments</subject><subject>Receptors, Formyl Peptide - biosynthesis</subject><subject>Receptors, Lipoxin - biosynthesis</subject><subject>T-Lymphocyte Subsets - immunology</subject><subject>T-Lymphocyte Subsets - metabolism</subject><subject>Young Adult</subject><issn>1567-5769</issn><issn>1878-1705</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNqFkU2P0zAQhi0EYpeFf4CQL4hTunbs2MkFqaqWD6kSF5C4WY4zFi6JHTzJavvvcWmBG5w8evWMPZ6HkJecbTjj6vawCXEJ07yp2a9ow5h6RK55q9uKa9Y8LnWjdNVo1V2RZ4gHxkou-VNyVbNOS8G6a-J3aZpttku4B2qjHY8YkCZPtzHCQ4h0yyuf8nQc6QzzEgagGVypUqb17Xb_lcLDnAExpEgL_m2dbKQjrN-TOy5Ace0RFnxOnng7Iry4nDfky7u7z7sP1f7T-4-77b5ysu2WyjUSxFB7J4TWvgNmtbKqGTRoIaH3snzO96wdvHB9y51qeldz39eKKWhgEDfkzfneOacfK-BipoAOxtFGSCuaVsmuUbxj_yelkLyWXBVSnkmXE2IGb-YcJpuPhjNzUmEO5qzCnFSc0qKitL26PLD2Ewx_mn7vvgCvL4BFZ0efbXQB_3JCq1bqunBvzxyUxd0HyAZdgOhgCEXFYoYU_j3JT8y7qlM</recordid><startdate>2011</startdate><enddate>2011</enddate><creator>Spurr, Lydia</creator><creator>Nadkarni, Suchita</creator><creator>Pederzoli-Ribeil, Magali</creator><creator>Goulding, Nicolas J.</creator><creator>Perretti, Mauro</creator><creator>D'Acquisto, Fulvio</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>IQODW</scope><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><scope>7T5</scope><scope>H94</scope></search><sort><creationdate>2011</creationdate><title>Comparative analysis of Annexin A1-formyl peptide receptor 2/ALX expression in human leukocyte subsets</title><author>Spurr, Lydia ; Nadkarni, Suchita ; Pederzoli-Ribeil, Magali ; Goulding, Nicolas J. ; Perretti, Mauro ; D'Acquisto, Fulvio</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c489t-c54e3d2fc3377f9e0a76a65d7e734ebf4878fb08df3cb81c65bc21fb2606e5ed3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Adaptive immune cells</topic><topic>Adult</topic><topic>Annexin A1 - biosynthesis</topic><topic>Annexin-A1</topic><topic>Autoimmune Diseases - metabolism</topic><topic>Biological and medical sciences</topic><topic>Blotting, Western</topic><topic>Female</topic><topic>Flow Cytometry</topic><topic>Formyl peptide receptor 2/ALX</topic><topic>Humans</topic><topic>Innate immune cells</topic><topic>Leukocytes - immunology</topic><topic>Leukocytes - metabolism</topic><topic>Leukocytes, Mononuclear - immunology</topic><topic>Leukocytes, Mononuclear - metabolism</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Neutrophils - immunology</topic><topic>Neutrophils - metabolism</topic><topic>Pharmacology. Drug treatments</topic><topic>Receptors, Formyl Peptide - biosynthesis</topic><topic>Receptors, Lipoxin - biosynthesis</topic><topic>T-Lymphocyte Subsets - immunology</topic><topic>T-Lymphocyte Subsets - metabolism</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Spurr, Lydia</creatorcontrib><creatorcontrib>Nadkarni, Suchita</creatorcontrib><creatorcontrib>Pederzoli-Ribeil, Magali</creatorcontrib><creatorcontrib>Goulding, Nicolas J.</creatorcontrib><creatorcontrib>Perretti, Mauro</creatorcontrib><creatorcontrib>D'Acquisto, Fulvio</creatorcontrib><collection>Pascal-Francis</collection><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><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>International immunopharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Spurr, Lydia</au><au>Nadkarni, Suchita</au><au>Pederzoli-Ribeil, Magali</au><au>Goulding, Nicolas J.</au><au>Perretti, Mauro</au><au>D'Acquisto, Fulvio</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparative analysis of Annexin A1-formyl peptide receptor 2/ALX expression in human leukocyte subsets</atitle><jtitle>International immunopharmacology</jtitle><addtitle>Int Immunopharmacol</addtitle><date>2011</date><risdate>2011</risdate><volume>11</volume><issue>1</issue><spage>55</spage><epage>66</epage><pages>55-66</pages><issn>1567-5769</issn><eissn>1878-1705</eissn><abstract>Recent studies have associated the dysregulated expression of Annexin-A1/Formyl peptide receptor 2 (FPR2/ALX) system with the development of autoimmune diseases. In this study we systematically scanned human leukocyte subsets for the presence of this pathway aiming to provide a roadmap that will help investigators to explore possible links between the development of immune related disorders and the expression of this system. Our results show that neutrophils, monocytes and NK cells express higher levels of both AnxA1 and FPR2/ALX compared to T or B cells. Further analysis of specific T cell subsets revealed higher levels in activated CD25
+ and memory CD45RO CD4 T cells compared to resting CD25
− or naïve CD45RA CD4 T cells. Together the results expand our knowledge of the AnxA1-FPR2/ALX system in immune cells and provide new avenues for investigation into the functions of this signalling pathway in systems other than that classically described for neutrophils.
►This is the first study showing FPR2/ALX as the genuine receptor for full-length Annexin-A1. ►This study demonstrated that Annexin-A1 modulates the strength of TCR signalling. ►A comprehensive review of the biological functions of formyl peptide receptors. ►This study provided the first evidence of Annexin-A1-derived peptides as ligand for formyl peptide receptors.</abstract><cop>Kidlington</cop><pub>Elsevier B.V</pub><pmid>20974309</pmid><doi>10.1016/j.intimp.2010.10.006</doi><tpages>12</tpages></addata></record> |
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subjects | Adaptive immune cells Adult Annexin A1 - biosynthesis Annexin-A1 Autoimmune Diseases - metabolism Biological and medical sciences Blotting, Western Female Flow Cytometry Formyl peptide receptor 2/ALX Humans Innate immune cells Leukocytes - immunology Leukocytes - metabolism Leukocytes, Mononuclear - immunology Leukocytes, Mononuclear - metabolism Male Medical sciences Neutrophils - immunology Neutrophils - metabolism Pharmacology. Drug treatments Receptors, Formyl Peptide - biosynthesis Receptors, Lipoxin - biosynthesis T-Lymphocyte Subsets - immunology T-Lymphocyte Subsets - metabolism Young Adult |
title | Comparative analysis of Annexin A1-formyl peptide receptor 2/ALX expression in human leukocyte subsets |
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