Annexin1 regulates DC efferocytosis and cross-presentation during Mycobacterium tuberculosis infection
The phagocytosis of apoptotic cells and associated vesicles (efferocytosis) by DCs is an important mechanism for both self tolerance and host defense. Although some of the engulfment ligands involved in efferocytosis have been identified and studied in vitro, the contributions of these ligands in vi...
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Veröffentlicht in: | The Journal of clinical investigation 2015-02, Vol.125 (2), p.752-768 |
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creator | Tzelepis, Fanny Verway, Mark Daoud, Jamal Gillard, Joshua Hassani-Ardakani, Kimya Dunn, Jonathan Downey, Jeffrey Gentile, Marilena Elena Jaworska, Joanna Sanchez, Anthony Michel Jean Nédélec, Yohann Vali, Hojatollah Tabrizian, Maryam Kristof, Arnold Scott King, Irah Luther Barreiro, Luis Bruno Divangahi, Maziar |
description | The phagocytosis of apoptotic cells and associated vesicles (efferocytosis) by DCs is an important mechanism for both self tolerance and host defense. Although some of the engulfment ligands involved in efferocytosis have been identified and studied in vitro, the contributions of these ligands in vivo remain ill defined. Here, we determined that during Mycobacterium tuberculosis (Mtb) infection, the engulfment ligand annexin1 is an important mediator in DC cross-presentation that increases efferocytosis in DCs and intrinsically enhances the capacity of the DC antigen-presenting machinery. Annexin1-deficient mice were highly susceptible to Mtb infection and showed an impaired Mtb antigen-specific CD8+ T cell response. Importantly, annexin1 expression was greatly downregulated in Mtb-infected human blood monocyte-derived DCs, indicating that reduction of annexin1 is a critical mechanism for immune evasion by Mtb. Collectively, these data indicate that annexin1 is essential in immunity to Mtb infection and mediates the power of DC efferocytosis and cross-presentation. |
doi_str_mv | 10.1172/JCI77014 |
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Although some of the engulfment ligands involved in efferocytosis have been identified and studied in vitro, the contributions of these ligands in vivo remain ill defined. Here, we determined that during Mycobacterium tuberculosis (Mtb) infection, the engulfment ligand annexin1 is an important mediator in DC cross-presentation that increases efferocytosis in DCs and intrinsically enhances the capacity of the DC antigen-presenting machinery. Annexin1-deficient mice were highly susceptible to Mtb infection and showed an impaired Mtb antigen-specific CD8+ T cell response. Importantly, annexin1 expression was greatly downregulated in Mtb-infected human blood monocyte-derived DCs, indicating that reduction of annexin1 is a critical mechanism for immune evasion by Mtb. Collectively, these data indicate that annexin1 is essential in immunity to Mtb infection and mediates the power of DC efferocytosis and cross-presentation.</description><identifier>ISSN: 0021-9738</identifier><identifier>EISSN: 1558-8238</identifier><identifier>DOI: 10.1172/JCI77014</identifier><identifier>PMID: 25562320</identifier><language>eng</language><publisher>United States: American Society for Clinical Investigation</publisher><subject>Animals ; Annexin A1 - genetics ; Annexin A1 - immunology ; Antigens ; Apoptosis ; Apoptotic proteins ; Autophagy ; Biomedical research ; CD8-Positive T-Lymphocytes - immunology ; CD8-Positive T-Lymphocytes - pathology ; Cross-Priming ; Dendritic Cells - immunology ; Dendritic Cells - pathology ; Distribution ; Drug dosages ; Gene expression ; Genomes ; Human health and pathology ; Humans ; Immunity, Cellular ; Infection ; Infections ; Life Sciences ; Ligands ; Lymphocytes ; Medical research ; Mice ; Mice, Knockout ; Monocytes - immunology ; Monocytes - pathology ; Mycobacterium tuberculosis ; Mycobacterium tuberculosis - immunology ; Phagocytosis ; Physiological aspects ; Properties ; Studies ; Tuberculosis ; Tuberculosis - genetics ; Tuberculosis - immunology ; Tuberculosis - pathology</subject><ispartof>The Journal of clinical investigation, 2015-02, Vol.125 (2), p.752-768</ispartof><rights>COPYRIGHT 2015 American Society for Clinical Investigation</rights><rights>Copyright American Society for Clinical Investigation Feb 2015</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><rights>Copyright © 2015, American Society for Clinical Investigation 2015 American Society for Clinical Investigation</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c737t-9e84ad20bc43b5494097355095a8aba15c49786b9231cf2d10329fd408a00c893</citedby><cites>FETCH-LOGICAL-c737t-9e84ad20bc43b5494097355095a8aba15c49786b9231cf2d10329fd408a00c893</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/PMC4319406/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4319406/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25562320$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-01141091$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Tzelepis, Fanny</creatorcontrib><creatorcontrib>Verway, Mark</creatorcontrib><creatorcontrib>Daoud, Jamal</creatorcontrib><creatorcontrib>Gillard, Joshua</creatorcontrib><creatorcontrib>Hassani-Ardakani, Kimya</creatorcontrib><creatorcontrib>Dunn, Jonathan</creatorcontrib><creatorcontrib>Downey, Jeffrey</creatorcontrib><creatorcontrib>Gentile, Marilena Elena</creatorcontrib><creatorcontrib>Jaworska, Joanna</creatorcontrib><creatorcontrib>Sanchez, Anthony Michel Jean</creatorcontrib><creatorcontrib>Nédélec, Yohann</creatorcontrib><creatorcontrib>Vali, Hojatollah</creatorcontrib><creatorcontrib>Tabrizian, Maryam</creatorcontrib><creatorcontrib>Kristof, Arnold Scott</creatorcontrib><creatorcontrib>King, Irah Luther</creatorcontrib><creatorcontrib>Barreiro, Luis Bruno</creatorcontrib><creatorcontrib>Divangahi, Maziar</creatorcontrib><title>Annexin1 regulates DC efferocytosis and cross-presentation during Mycobacterium tuberculosis infection</title><title>The Journal of clinical investigation</title><addtitle>J Clin Invest</addtitle><description>The phagocytosis of apoptotic cells and associated vesicles (efferocytosis) by DCs is an important mechanism for both self tolerance and host defense. Although some of the engulfment ligands involved in efferocytosis have been identified and studied in vitro, the contributions of these ligands in vivo remain ill defined. Here, we determined that during Mycobacterium tuberculosis (Mtb) infection, the engulfment ligand annexin1 is an important mediator in DC cross-presentation that increases efferocytosis in DCs and intrinsically enhances the capacity of the DC antigen-presenting machinery. Annexin1-deficient mice were highly susceptible to Mtb infection and showed an impaired Mtb antigen-specific CD8+ T cell response. Importantly, annexin1 expression was greatly downregulated in Mtb-infected human blood monocyte-derived DCs, indicating that reduction of annexin1 is a critical mechanism for immune evasion by Mtb. Collectively, these data indicate that annexin1 is essential in immunity to Mtb infection and mediates the power of DC efferocytosis and cross-presentation.</description><subject>Animals</subject><subject>Annexin A1 - genetics</subject><subject>Annexin A1 - immunology</subject><subject>Antigens</subject><subject>Apoptosis</subject><subject>Apoptotic proteins</subject><subject>Autophagy</subject><subject>Biomedical research</subject><subject>CD8-Positive T-Lymphocytes - immunology</subject><subject>CD8-Positive T-Lymphocytes - pathology</subject><subject>Cross-Priming</subject><subject>Dendritic Cells - immunology</subject><subject>Dendritic Cells - pathology</subject><subject>Distribution</subject><subject>Drug dosages</subject><subject>Gene expression</subject><subject>Genomes</subject><subject>Human health and pathology</subject><subject>Humans</subject><subject>Immunity, Cellular</subject><subject>Infection</subject><subject>Infections</subject><subject>Life Sciences</subject><subject>Ligands</subject><subject>Lymphocytes</subject><subject>Medical research</subject><subject>Mice</subject><subject>Mice, Knockout</subject><subject>Monocytes - immunology</subject><subject>Monocytes - pathology</subject><subject>Mycobacterium tuberculosis</subject><subject>Mycobacterium tuberculosis - immunology</subject><subject>Phagocytosis</subject><subject>Physiological aspects</subject><subject>Properties</subject><subject>Studies</subject><subject>Tuberculosis</subject><subject>Tuberculosis - genetics</subject><subject>Tuberculosis - immunology</subject><subject>Tuberculosis - pathology</subject><issn>0021-9738</issn><issn>1558-8238</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BEC</sourceid><sourceid>BENPR</sourceid><recordid>eNqNk0tr3DAQx01pabZpoZ-gGAqlOTiVZMmyL4Vl-8iWLYG-rkKWx14Fr7SV5JD99pWTTRqHPQQdBKPf_OehmSR5jdEpxpx8-LZYco4wfZLMMGNlVpK8fJrMECI4q3heHiUvvL9AkaCMPk-OCGMFyQmaJe3cGLjSBqcOuqGXAXz6aZFC24Kzahes1z6VpkmVs95nWwceTJBBW5M2g9OmS7_vlK2lCuD0sEnDUINTQ3_tqE0LamRfJs9a2Xt4tb-Pk99fPv9anGWr86_LxXyVKZ7zkFVQUtkQVCua14xWFMXsGUMVk6WsJWaKVrws6orkWLWkwSgnVdtQVEqEVFnlx8nHG93tUG-gUTFXJ3uxdXoj3U5YqcX0xei16OyloDmO0YoocHIjsH7gdjZfidGGMKYYVfgSR_b9PpizfwfwQWy0V9D30oAdvMBFUZKCM0IegTJCC4Q5jejbB-iFHZyJXRsFCeKxTPyf6mQPIvbZxnLUKCrmNOpwThiPVHaA6sBArN0aaHU0T_jTA3w8DWy0OuhwMnGITICr0MnBe7H8-ePx7PmfKfvuHrsG2Ye1t_0wzpKfgvvGXs-ng_bu0zAS426I292I6Jv7s3EH3i5D_g9W5QP0</recordid><startdate>20150201</startdate><enddate>20150201</enddate><creator>Tzelepis, Fanny</creator><creator>Verway, Mark</creator><creator>Daoud, Jamal</creator><creator>Gillard, Joshua</creator><creator>Hassani-Ardakani, Kimya</creator><creator>Dunn, Jonathan</creator><creator>Downey, Jeffrey</creator><creator>Gentile, Marilena Elena</creator><creator>Jaworska, Joanna</creator><creator>Sanchez, Anthony Michel Jean</creator><creator>Nédélec, Yohann</creator><creator>Vali, Hojatollah</creator><creator>Tabrizian, Maryam</creator><creator>Kristof, Arnold Scott</creator><creator>King, Irah Luther</creator><creator>Barreiro, Luis Bruno</creator><creator>Divangahi, Maziar</creator><general>American Society for Clinical Investigation</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>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</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>BEC</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>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>S0X</scope><scope>7X8</scope><scope>7QL</scope><scope>7T5</scope><scope>C1K</scope><scope>H94</scope><scope>1XC</scope><scope>VOOES</scope><scope>5PM</scope></search><sort><creationdate>20150201</creationdate><title>Annexin1 regulates DC efferocytosis and cross-presentation during Mycobacterium tuberculosis infection</title><author>Tzelepis, Fanny ; Verway, Mark ; Daoud, Jamal ; Gillard, Joshua ; Hassani-Ardakani, Kimya ; Dunn, Jonathan ; Downey, Jeffrey ; Gentile, Marilena Elena ; Jaworska, Joanna ; Sanchez, Anthony Michel Jean ; Nédélec, Yohann ; Vali, Hojatollah ; Tabrizian, Maryam ; Kristof, Arnold Scott ; King, Irah Luther ; Barreiro, Luis Bruno ; Divangahi, Maziar</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c737t-9e84ad20bc43b5494097355095a8aba15c49786b9231cf2d10329fd408a00c893</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Animals</topic><topic>Annexin A1 - 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Although some of the engulfment ligands involved in efferocytosis have been identified and studied in vitro, the contributions of these ligands in vivo remain ill defined. Here, we determined that during Mycobacterium tuberculosis (Mtb) infection, the engulfment ligand annexin1 is an important mediator in DC cross-presentation that increases efferocytosis in DCs and intrinsically enhances the capacity of the DC antigen-presenting machinery. Annexin1-deficient mice were highly susceptible to Mtb infection and showed an impaired Mtb antigen-specific CD8+ T cell response. Importantly, annexin1 expression was greatly downregulated in Mtb-infected human blood monocyte-derived DCs, indicating that reduction of annexin1 is a critical mechanism for immune evasion by Mtb. 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subjects | Animals Annexin A1 - genetics Annexin A1 - immunology Antigens Apoptosis Apoptotic proteins Autophagy Biomedical research CD8-Positive T-Lymphocytes - immunology CD8-Positive T-Lymphocytes - pathology Cross-Priming Dendritic Cells - immunology Dendritic Cells - pathology Distribution Drug dosages Gene expression Genomes Human health and pathology Humans Immunity, Cellular Infection Infections Life Sciences Ligands Lymphocytes Medical research Mice Mice, Knockout Monocytes - immunology Monocytes - pathology Mycobacterium tuberculosis Mycobacterium tuberculosis - immunology Phagocytosis Physiological aspects Properties Studies Tuberculosis Tuberculosis - genetics Tuberculosis - immunology Tuberculosis - pathology |
title | Annexin1 regulates DC efferocytosis and cross-presentation during Mycobacterium tuberculosis infection |
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