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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:International immunology 2002-09, Vol.14 (9), p.1003-1014
Hauptverfasser: Castaigne, Jean‐Gabriel, Guo, Wenyan, Lévéille, Claire, Charron, Dominique, Al‐Daccak, Reem
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1014
container_issue 9
container_start_page 1003
container_title International immunology
container_volume 14
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
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_72043249</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>72043249</sourcerecordid><originalsourceid>FETCH-LOGICAL-c426t-67039147c0bf6345f4ee56f7098432c0f1dc5d599dd0fadbf0ccaad783e40a573</originalsourceid><addsrcrecordid>eNqFkcFOGzEQhq0K1ITQY6-VT70tjNfe9foYBQoVkRBSKyEulmOPwU12N107hdx4hD5LH6QPwZOwkIgcucwc_k-_Zv6fkM8MjhgofhyaFOr62D14kOwDGTJRQpZzKffIEFTBs4rJakAOYvwFADxX_CMZsDyHnKtqSG7HdHLCqqfHvw6X2DhsEl12bcLQ0HloTEQ6of__9XqNLpiEjppFwq4xKfxBanGxoA5NuqPLftybNW09NbYXX9m6bVq7ThgPyb43i4iftntEfn47_TE5z6aXZ98n42lmRV6mrJTAFRPSwsyXXBReIBall6AqwXMLnjlbuEIp58AbN_NgrTFOVhwFmELyEfm68e2f-L3CmHQd4suVpsF2FbXMoTcS6l2QVSUIBWUPZhvQdm2MHXq97EJturVmoF8q0JsK9KaCnv-yNV7N-sx29DbznWGICR_edNPNdSm5LPT59Y0GLq9u-NmFPuHPVKSWog</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>18604906</pqid></control><display><type>article</type><title>A CD18‐dependent protein kinase C β‐mediated alternative cell death pathway of activated monocytes</title><source>Oxford University Press Journals All Titles (1996-Current)</source><source>MEDLINE</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>Alma/SFX Local Collection</source><creator>Castaigne, Jean‐Gabriel ; Guo, Wenyan ; Lévéille, Claire ; Charron, Dominique ; Al‐Daccak, Reem</creator><creatorcontrib>Castaigne, Jean‐Gabriel ; Guo, Wenyan ; Lévéille, Claire ; Charron, Dominique ; Al‐Daccak, Reem</creatorcontrib><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><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>
fulltext fulltext
identifier ISSN: 0953-8178
ispartof International immunology, 2002-09, Vol.14 (9), p.1003-1014
issn 0953-8178
1460-2377
1460-2377
language eng
recordid cdi_proquest_miscellaneous_72043249
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
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-02T12%3A17%3A33IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=A%20CD18%E2%80%90dependent%20protein%20kinase%20C%20%CE%B2%E2%80%90mediated%20alternative%20cell%20death%20pathway%20of%20activated%20monocytes&rft.jtitle=International%20immunology&rft.au=Castaigne,%20Jean%E2%80%90Gabriel&rft.date=2002-09&rft.volume=14&rft.issue=9&rft.spage=1003&rft.epage=1014&rft.pages=1003-1014&rft.issn=0953-8178&rft.eissn=1460-2377&rft_id=info:doi/10.1093/intimm/dxf071&rft_dat=%3Cproquest_cross%3E72043249%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=18604906&rft_id=info:pmid/12202398&rfr_iscdi=true