A CD18‐dependent protein kinase C β‐mediated alternative cell death pathway of activated monocytes
Activated monocytes become resistant to numerous death stimuli including death receptors. Given that the uncontrolled activation of monocytes/macrophages and their persistence can lead to severe inflammatory conditions, it is critical to define the pathways that control their elimination. We previou...
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Veröffentlicht in: | International immunology 2002-09, Vol.14 (9), p.1003-1014 |
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creator | Castaigne, Jean‐Gabriel Guo, Wenyan Lévéille, Claire Charron, Dominique Al‐Daccak, Reem |
description | Activated monocytes become resistant to numerous death stimuli including death receptors. Given that the uncontrolled activation of monocytes/macrophages and their persistence can lead to severe inflammatory conditions, it is critical to define the pathways that control their elimination. We previously reported that ligation of HLA‐DR molecules on peripheral blood‐derived monocytes induces their death. To investigate the mechanisms of HLA‐DR‐mediated death in monocytes, we used the THP‐1 monocytic cell line as a model. We show that while THP‐1 are equally resistant to HLA‐DR‐ and to Fas‐mediated death, treatment of THP‐1 with IFN‐γ renders them sensitive to HLA‐DR‐ but not to Fas‐mediated death. Both activation of the Src family protein tyrosine kinase and classical protein kinase C (PKC) occur through HLA‐DR, but only PKC activation is involved in HLA‐DR‐mediated death of these cells. Moreover, HLA‐DR‐mediated cell death of activated monocytes implicates a regulatory loop between the HLA‐DR/CD18 complex and the downstream activation of PKCβ. Thus, our study identifies an alternative physiological signaling pathway of monocyte death, and further investigation on its regulation is likely to provide significant insights into the control of monocyte homeostasis and inflammation. |
doi_str_mv | 10.1093/intimm/dxf071 |
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Given that the uncontrolled activation of monocytes/macrophages and their persistence can lead to severe inflammatory conditions, it is critical to define the pathways that control their elimination. We previously reported that ligation of HLA‐DR molecules on peripheral blood‐derived monocytes induces their death. To investigate the mechanisms of HLA‐DR‐mediated death in monocytes, we used the THP‐1 monocytic cell line as a model. We show that while THP‐1 are equally resistant to HLA‐DR‐ and to Fas‐mediated death, treatment of THP‐1 with IFN‐γ renders them sensitive to HLA‐DR‐ but not to Fas‐mediated death. Both activation of the Src family protein tyrosine kinase and classical protein kinase C (PKC) occur through HLA‐DR, but only PKC activation is involved in HLA‐DR‐mediated death of these cells. Moreover, HLA‐DR‐mediated cell death of activated monocytes implicates a regulatory loop between the HLA‐DR/CD18 complex and the downstream activation of PKCβ. Thus, our study identifies an alternative physiological signaling pathway of monocyte death, and further investigation on its regulation is likely to provide significant insights into the control of monocyte homeostasis and inflammation.</description><identifier>ISSN: 0953-8178</identifier><identifier>ISSN: 1460-2377</identifier><identifier>EISSN: 1460-2377</identifier><identifier>DOI: 10.1093/intimm/dxf071</identifier><identifier>PMID: 12202398</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>apoptosis ; CD18 Antigens - physiology ; Cell Death - physiology ; Cell Line ; Histocompatibility Antigens Class II - immunology ; Histocompatibility Antigens Class II - physiology ; HLA-DR Antigens - immunology ; HLA-DR Antigens - physiology ; Humans ; integrins ; Interferon-gamma - pharmacology ; macrophages ; MHC class II ; Monocytes - drug effects ; Monocytes - physiology ; Precipitin Tests ; Protein Kinase C - physiology ; Protein Kinase C beta ; protein tyrosine kinase ; Signal Transduction ; signaling</subject><ispartof>International immunology, 2002-09, Vol.14 (9), p.1003-1014</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c426t-67039147c0bf6345f4ee56f7098432c0f1dc5d599dd0fadbf0ccaad783e40a573</citedby></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/12202398$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Castaigne, Jean‐Gabriel</creatorcontrib><creatorcontrib>Guo, Wenyan</creatorcontrib><creatorcontrib>Lévéille, Claire</creatorcontrib><creatorcontrib>Charron, Dominique</creatorcontrib><creatorcontrib>Al‐Daccak, Reem</creatorcontrib><title>A CD18‐dependent protein kinase C β‐mediated alternative cell death pathway of activated monocytes</title><title>International immunology</title><addtitle>Int. Immunol</addtitle><description>Activated monocytes become resistant to numerous death stimuli including death receptors. Given that the uncontrolled activation of monocytes/macrophages and their persistence can lead to severe inflammatory conditions, it is critical to define the pathways that control their elimination. We previously reported that ligation of HLA‐DR molecules on peripheral blood‐derived monocytes induces their death. To investigate the mechanisms of HLA‐DR‐mediated death in monocytes, we used the THP‐1 monocytic cell line as a model. We show that while THP‐1 are equally resistant to HLA‐DR‐ and to Fas‐mediated death, treatment of THP‐1 with IFN‐γ renders them sensitive to HLA‐DR‐ but not to Fas‐mediated death. Both activation of the Src family protein tyrosine kinase and classical protein kinase C (PKC) occur through HLA‐DR, but only PKC activation is involved in HLA‐DR‐mediated death of these cells. Moreover, HLA‐DR‐mediated cell death of activated monocytes implicates a regulatory loop between the HLA‐DR/CD18 complex and the downstream activation of PKCβ. Thus, our study identifies an alternative physiological signaling pathway of monocyte death, and further investigation on its regulation is likely to provide significant insights into the control of monocyte homeostasis and inflammation.</description><subject>apoptosis</subject><subject>CD18 Antigens - physiology</subject><subject>Cell Death - physiology</subject><subject>Cell Line</subject><subject>Histocompatibility Antigens Class II - immunology</subject><subject>Histocompatibility Antigens Class II - physiology</subject><subject>HLA-DR Antigens - immunology</subject><subject>HLA-DR Antigens - physiology</subject><subject>Humans</subject><subject>integrins</subject><subject>Interferon-gamma - pharmacology</subject><subject>macrophages</subject><subject>MHC class II</subject><subject>Monocytes - drug effects</subject><subject>Monocytes - physiology</subject><subject>Precipitin Tests</subject><subject>Protein Kinase C - physiology</subject><subject>Protein Kinase C beta</subject><subject>protein tyrosine kinase</subject><subject>Signal Transduction</subject><subject>signaling</subject><issn>0953-8178</issn><issn>1460-2377</issn><issn>1460-2377</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkcFOGzEQhq0K1ITQY6-VT70tjNfe9foYBQoVkRBSKyEulmOPwU12N107hdx4hD5LH6QPwZOwkIgcucwc_k-_Zv6fkM8MjhgofhyaFOr62D14kOwDGTJRQpZzKffIEFTBs4rJakAOYvwFADxX_CMZsDyHnKtqSG7HdHLCqqfHvw6X2DhsEl12bcLQ0HloTEQ6of__9XqNLpiEjppFwq4xKfxBanGxoA5NuqPLftybNW09NbYXX9m6bVq7ThgPyb43i4iftntEfn47_TE5z6aXZ98n42lmRV6mrJTAFRPSwsyXXBReIBall6AqwXMLnjlbuEIp58AbN_NgrTFOVhwFmELyEfm68e2f-L3CmHQd4suVpsF2FbXMoTcS6l2QVSUIBWUPZhvQdm2MHXq97EJturVmoF8q0JsK9KaCnv-yNV7N-sx29DbznWGICR_edNPNdSm5LPT59Y0GLq9u-NmFPuHPVKSWog</recordid><startdate>200209</startdate><enddate>200209</enddate><creator>Castaigne, Jean‐Gabriel</creator><creator>Guo, Wenyan</creator><creator>Lévéille, Claire</creator><creator>Charron, Dominique</creator><creator>Al‐Daccak, Reem</creator><general>Oxford University Press</general><scope>BSCLL</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>7T5</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>200209</creationdate><title>A CD18‐dependent protein kinase C β‐mediated alternative cell death pathway of activated monocytes</title><author>Castaigne, Jean‐Gabriel ; Guo, Wenyan ; Lévéille, Claire ; Charron, Dominique ; Al‐Daccak, Reem</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c426t-67039147c0bf6345f4ee56f7098432c0f1dc5d599dd0fadbf0ccaad783e40a573</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>apoptosis</topic><topic>CD18 Antigens - physiology</topic><topic>Cell Death - physiology</topic><topic>Cell Line</topic><topic>Histocompatibility Antigens Class II - immunology</topic><topic>Histocompatibility Antigens Class II - physiology</topic><topic>HLA-DR Antigens - immunology</topic><topic>HLA-DR Antigens - physiology</topic><topic>Humans</topic><topic>integrins</topic><topic>Interferon-gamma - pharmacology</topic><topic>macrophages</topic><topic>MHC class II</topic><topic>Monocytes - drug effects</topic><topic>Monocytes - physiology</topic><topic>Precipitin Tests</topic><topic>Protein Kinase C - physiology</topic><topic>Protein Kinase C beta</topic><topic>protein tyrosine kinase</topic><topic>Signal Transduction</topic><topic>signaling</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Castaigne, Jean‐Gabriel</creatorcontrib><creatorcontrib>Guo, Wenyan</creatorcontrib><creatorcontrib>Lévéille, Claire</creatorcontrib><creatorcontrib>Charron, Dominique</creatorcontrib><creatorcontrib>Al‐Daccak, Reem</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>International immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Castaigne, Jean‐Gabriel</au><au>Guo, Wenyan</au><au>Lévéille, Claire</au><au>Charron, Dominique</au><au>Al‐Daccak, Reem</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A CD18‐dependent protein kinase C β‐mediated alternative cell death pathway of activated monocytes</atitle><jtitle>International immunology</jtitle><addtitle>Int. Immunol</addtitle><date>2002-09</date><risdate>2002</risdate><volume>14</volume><issue>9</issue><spage>1003</spage><epage>1014</epage><pages>1003-1014</pages><issn>0953-8178</issn><issn>1460-2377</issn><eissn>1460-2377</eissn><abstract>Activated monocytes become resistant to numerous death stimuli including death receptors. Given that the uncontrolled activation of monocytes/macrophages and their persistence can lead to severe inflammatory conditions, it is critical to define the pathways that control their elimination. We previously reported that ligation of HLA‐DR molecules on peripheral blood‐derived monocytes induces their death. To investigate the mechanisms of HLA‐DR‐mediated death in monocytes, we used the THP‐1 monocytic cell line as a model. We show that while THP‐1 are equally resistant to HLA‐DR‐ and to Fas‐mediated death, treatment of THP‐1 with IFN‐γ renders them sensitive to HLA‐DR‐ but not to Fas‐mediated death. Both activation of the Src family protein tyrosine kinase and classical protein kinase C (PKC) occur through HLA‐DR, but only PKC activation is involved in HLA‐DR‐mediated death of these cells. Moreover, HLA‐DR‐mediated cell death of activated monocytes implicates a regulatory loop between the HLA‐DR/CD18 complex and the downstream activation of PKCβ. Thus, our study identifies an alternative physiological signaling pathway of monocyte death, and further investigation on its regulation is likely to provide significant insights into the control of monocyte homeostasis and inflammation.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>12202398</pmid><doi>10.1093/intimm/dxf071</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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source | Oxford University Press Journals All Titles (1996-Current); MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection |
subjects | apoptosis CD18 Antigens - physiology Cell Death - physiology Cell Line Histocompatibility Antigens Class II - immunology Histocompatibility Antigens Class II - physiology HLA-DR Antigens - immunology HLA-DR Antigens - physiology Humans integrins Interferon-gamma - pharmacology macrophages MHC class II Monocytes - drug effects Monocytes - physiology Precipitin Tests Protein Kinase C - physiology Protein Kinase C beta protein tyrosine kinase Signal Transduction signaling |
title | A CD18‐dependent protein kinase C β‐mediated alternative cell death pathway of activated monocytes |
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