PKCtheta signals activation versus tolerance in vivo
Understanding the pathways that signal T cell tolerance versus activation is key to regulating immunity. Previous studies have linked CD28 and protein kinase C-theta (PKCtheta) as a potential signaling pathway that influences T cell activation. Therefore, we have compared the responses of T cells de...
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Veröffentlicht in: | The Journal of experimental medicine 2004-03, Vol.199 (6), p.743-752 |
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container_title | The Journal of experimental medicine |
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creator | Berg-Brown, Nancy N Gronski, Matthew A Jones, Russell G Elford, Alisha R Deenick, Elissa K Odermatt, Bernhard Littman, Dan R Ohashi, Pamela S |
description | Understanding the pathways that signal T cell tolerance versus activation is key to regulating immunity. Previous studies have linked CD28 and protein kinase C-theta (PKCtheta) as a potential signaling pathway that influences T cell activation. Therefore, we have compared the responses of T cells deficient for CD28 and PKCtheta in vivo and in vitro. Here, we demonstrate that the absence of PKCtheta leads to the induction of T cell anergy, with a phenotype that is comparable to the absence of CD28. Further experiments examined whether PKCtheta triggered other CD28-dependent responses. Our data show that CD4 T cell-B cell cooperation is dependent on CD28 but not PKCtheta, whereas CD28 costimulatory signals that augment proliferation can be uncoupled from signals that regulate anergy. Therefore, PKCtheta relays a defined subset of CD28 signals during T cell activation and is critical for the induction of activation versus tolerance in vivo. |
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Previous studies have linked CD28 and protein kinase C-theta (PKCtheta) as a potential signaling pathway that influences T cell activation. Therefore, we have compared the responses of T cells deficient for CD28 and PKCtheta in vivo and in vitro. Here, we demonstrate that the absence of PKCtheta leads to the induction of T cell anergy, with a phenotype that is comparable to the absence of CD28. Further experiments examined whether PKCtheta triggered other CD28-dependent responses. Our data show that CD4 T cell-B cell cooperation is dependent on CD28 but not PKCtheta, whereas CD28 costimulatory signals that augment proliferation can be uncoupled from signals that regulate anergy. Therefore, PKCtheta relays a defined subset of CD28 signals during T cell activation and is critical for the induction of activation versus tolerance in vivo.</description><identifier>ISSN: 0022-1007</identifier><identifier>PMID: 15024044</identifier><language>eng</language><publisher>United States</publisher><subject>Animals ; B-Lymphocytes - immunology ; CD28 Antigens - immunology ; CD28 Antigens - metabolism ; CD4 Antigens - immunology ; Clonal Anergy - immunology ; Flow Cytometry ; Immunohistochemistry ; Isoenzymes - immunology ; Isoenzymes - metabolism ; Lymphocyte Activation - immunology ; Mice ; Mice, Knockout ; Mice, Transgenic ; Protein Kinase C - immunology ; Protein Kinase C - metabolism ; Protein Kinase C-theta ; Signal Transduction - immunology ; T-Lymphocytes - immunology ; Vesicular stomatitis Indiana virus</subject><ispartof>The Journal of experimental medicine, 2004-03, Vol.199 (6), p.743-752</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15024044$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Berg-Brown, Nancy N</creatorcontrib><creatorcontrib>Gronski, Matthew A</creatorcontrib><creatorcontrib>Jones, Russell G</creatorcontrib><creatorcontrib>Elford, Alisha R</creatorcontrib><creatorcontrib>Deenick, Elissa K</creatorcontrib><creatorcontrib>Odermatt, Bernhard</creatorcontrib><creatorcontrib>Littman, Dan R</creatorcontrib><creatorcontrib>Ohashi, Pamela S</creatorcontrib><title>PKCtheta signals activation versus tolerance in vivo</title><title>The Journal of experimental medicine</title><addtitle>J Exp Med</addtitle><description>Understanding the pathways that signal T cell tolerance versus activation is key to regulating immunity. Previous studies have linked CD28 and protein kinase C-theta (PKCtheta) as a potential signaling pathway that influences T cell activation. Therefore, we have compared the responses of T cells deficient for CD28 and PKCtheta in vivo and in vitro. Here, we demonstrate that the absence of PKCtheta leads to the induction of T cell anergy, with a phenotype that is comparable to the absence of CD28. Further experiments examined whether PKCtheta triggered other CD28-dependent responses. Our data show that CD4 T cell-B cell cooperation is dependent on CD28 but not PKCtheta, whereas CD28 costimulatory signals that augment proliferation can be uncoupled from signals that regulate anergy. Therefore, PKCtheta relays a defined subset of CD28 signals during T cell activation and is critical for the induction of activation versus tolerance in vivo.</description><subject>Animals</subject><subject>B-Lymphocytes - immunology</subject><subject>CD28 Antigens - immunology</subject><subject>CD28 Antigens - metabolism</subject><subject>CD4 Antigens - immunology</subject><subject>Clonal Anergy - immunology</subject><subject>Flow Cytometry</subject><subject>Immunohistochemistry</subject><subject>Isoenzymes - immunology</subject><subject>Isoenzymes - metabolism</subject><subject>Lymphocyte Activation - immunology</subject><subject>Mice</subject><subject>Mice, Knockout</subject><subject>Mice, Transgenic</subject><subject>Protein Kinase C - immunology</subject><subject>Protein Kinase C - metabolism</subject><subject>Protein Kinase C-theta</subject><subject>Signal Transduction - immunology</subject><subject>T-Lymphocytes - immunology</subject><subject>Vesicular stomatitis Indiana virus</subject><issn>0022-1007</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo1j0tLxDAUhbNQZsZx_oJ05a5wm2ezlOILB3Qx-5I0txrpyyYt-O8NOLM68PFxOOeK7AAozQsAtSU3IXwDFJwLuSHbQgDlwPmO8I-3Kn5hNFnwn4PpQmaa6FcT_ThkK85hCVkcO5zN0GDmE_PreEuu26Ti4Zx7cnp6PFUv-fH9-bV6OOaT4DwvUQEzNo1QmtHSYNk4rU0reCLIpAXKpJJA29IxkFIo6rhzjVXaaksd25P7_9ppHn8WDLHufWiw68yA4xJqVSiqlBBJvDuLi-3R1dPsezP_1peb7A9_50wh</recordid><startdate>20040315</startdate><enddate>20040315</enddate><creator>Berg-Brown, Nancy N</creator><creator>Gronski, Matthew A</creator><creator>Jones, Russell G</creator><creator>Elford, Alisha R</creator><creator>Deenick, Elissa K</creator><creator>Odermatt, Bernhard</creator><creator>Littman, Dan R</creator><creator>Ohashi, Pamela S</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>20040315</creationdate><title>PKCtheta signals activation versus tolerance in vivo</title><author>Berg-Brown, Nancy N ; Gronski, Matthew A ; Jones, Russell G ; Elford, Alisha R ; Deenick, Elissa K ; Odermatt, Bernhard ; Littman, Dan R ; Ohashi, Pamela S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p544-8e703ab00279328ae8cd99af54027e36b02367602f8d3066572d4ddcb79b9b2d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Animals</topic><topic>B-Lymphocytes - immunology</topic><topic>CD28 Antigens - immunology</topic><topic>CD28 Antigens - metabolism</topic><topic>CD4 Antigens - immunology</topic><topic>Clonal Anergy - immunology</topic><topic>Flow Cytometry</topic><topic>Immunohistochemistry</topic><topic>Isoenzymes - immunology</topic><topic>Isoenzymes - metabolism</topic><topic>Lymphocyte Activation - immunology</topic><topic>Mice</topic><topic>Mice, Knockout</topic><topic>Mice, Transgenic</topic><topic>Protein Kinase C - immunology</topic><topic>Protein Kinase C - metabolism</topic><topic>Protein Kinase C-theta</topic><topic>Signal Transduction - immunology</topic><topic>T-Lymphocytes - immunology</topic><topic>Vesicular stomatitis Indiana virus</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Berg-Brown, Nancy N</creatorcontrib><creatorcontrib>Gronski, Matthew A</creatorcontrib><creatorcontrib>Jones, Russell G</creatorcontrib><creatorcontrib>Elford, Alisha R</creatorcontrib><creatorcontrib>Deenick, Elissa K</creatorcontrib><creatorcontrib>Odermatt, Bernhard</creatorcontrib><creatorcontrib>Littman, Dan R</creatorcontrib><creatorcontrib>Ohashi, Pamela S</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of experimental medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Berg-Brown, Nancy N</au><au>Gronski, Matthew A</au><au>Jones, Russell G</au><au>Elford, Alisha R</au><au>Deenick, Elissa K</au><au>Odermatt, Bernhard</au><au>Littman, Dan R</au><au>Ohashi, Pamela S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>PKCtheta signals activation versus tolerance in vivo</atitle><jtitle>The Journal of experimental medicine</jtitle><addtitle>J Exp Med</addtitle><date>2004-03-15</date><risdate>2004</risdate><volume>199</volume><issue>6</issue><spage>743</spage><epage>752</epage><pages>743-752</pages><issn>0022-1007</issn><abstract>Understanding the pathways that signal T cell tolerance versus activation is key to regulating immunity. Previous studies have linked CD28 and protein kinase C-theta (PKCtheta) as a potential signaling pathway that influences T cell activation. Therefore, we have compared the responses of T cells deficient for CD28 and PKCtheta in vivo and in vitro. Here, we demonstrate that the absence of PKCtheta leads to the induction of T cell anergy, with a phenotype that is comparable to the absence of CD28. Further experiments examined whether PKCtheta triggered other CD28-dependent responses. Our data show that CD4 T cell-B cell cooperation is dependent on CD28 but not PKCtheta, whereas CD28 costimulatory signals that augment proliferation can be uncoupled from signals that regulate anergy. Therefore, PKCtheta relays a defined subset of CD28 signals during T cell activation and is critical for the induction of activation versus tolerance in vivo.</abstract><cop>United States</cop><pmid>15024044</pmid><tpages>10</tpages></addata></record> |
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subjects | Animals B-Lymphocytes - immunology CD28 Antigens - immunology CD28 Antigens - metabolism CD4 Antigens - immunology Clonal Anergy - immunology Flow Cytometry Immunohistochemistry Isoenzymes - immunology Isoenzymes - metabolism Lymphocyte Activation - immunology Mice Mice, Knockout Mice, Transgenic Protein Kinase C - immunology Protein Kinase C - metabolism Protein Kinase C-theta Signal Transduction - immunology T-Lymphocytes - immunology Vesicular stomatitis Indiana virus |
title | PKCtheta signals activation versus tolerance in vivo |
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