Loading…

Translocation of PKCθ in T cells is mediated by a nonconventional, PI3-K– and Vav-dependent pathway, but does not absolutely require phospholipase C

PKCθ plays an essential role in activation of mature T cells via stimulation of AP-1 and NF-κB, and is known to selectively translocate to the immunological synapse in antigen-stimulated T cells. Recently, we reported that a Vav/Rac pathway which depends on actin cytoskeleton reorganization mediates...

Full description

Saved in:
Bibliographic Details
Published in:The Journal of cell biology 2002-04, Vol.157 (2), p.253-263
Main Authors: Villalba, Martin, Bi, Kun, Hu, Junru, Altman, Yoav, Bushway, Paul, Reits, Eric, Neefjes, Jacques, Baier, Gottfried, Abraham, Robert T., Altman, Amnon
Format: Article
Language:English
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c2447-94635fc2563883a7594d91c92c64ba0f9ded2e473a3c8643bc495ff3991a47613
cites cdi_FETCH-LOGICAL-c2447-94635fc2563883a7594d91c92c64ba0f9ded2e473a3c8643bc495ff3991a47613
container_end_page 263
container_issue 2
container_start_page 253
container_title The Journal of cell biology
container_volume 157
creator Villalba, Martin
Bi, Kun
Hu, Junru
Altman, Yoav
Bushway, Paul
Reits, Eric
Neefjes, Jacques
Baier, Gottfried
Abraham, Robert T.
Altman, Amnon
description PKCθ plays an essential role in activation of mature T cells via stimulation of AP-1 and NF-κB, and is known to selectively translocate to the immunological synapse in antigen-stimulated T cells. Recently, we reported that a Vav/Rac pathway which depends on actin cytoskeleton reorganization mediates selective recruitment of PKCθ to the membrane or cytoskeleton and its catalytic activation by anti-CD3/CD28 costimulation. Because this pathway acted selectively on PKCθ, we addressed here the question of whether the translocation and activation of PKCθ in T cells is regulated by a unique pathway distinct from the conventional mechanism for PKC activation, i.e., PLC-mediated production of DAG. Using three independent approaches, i.e., a selective PLC inhibitor, a PLCγ1-deficient T cell line, or a dominant negative PLCγ1 mutant, we demonstrate that CD3/CD28-induced membrane recruitment and COOH-terminal phosphorylation of PKCθ are largely independent of PLC. In contrast, the same inhibitory strategies blocked the membrane translocation of PKCα. Membrane or lipid raft recruitment of PKCθ (but not PKCα) was absent in T cells treated with phosphatidylinositol 3-kinase (PI3-K) inhibitors or in Vav-deficient T cells, and was enhanced by constitutively active PI3-K. 3-phosphoinositide-dependent kinase-1 (PDK1) also upregulated the membrane translocation of PKCθ, but did not associate with it. These results provide evidence that a nonconventional PI3-K– and Vav-dependent pathway mediates the selective membrane recruitment and, possibly, activation of PKCθ in T cells.
doi_str_mv 10.1083/jcb.200201097
format article
fullrecord <record><control><sourceid>pubmedcentral_cross</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2199257</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>pubmedcentral_primary_oai_pubmedcentral_nih_gov_2199257</sourcerecordid><originalsourceid>FETCH-LOGICAL-c2447-94635fc2563883a7594d91c92c64ba0f9ded2e473a3c8643bc495ff3991a47613</originalsourceid><addsrcrecordid>eNpVkU1O3EAQhVtRUJhAltnXAfDQv7Z7EykaBYIGiVkMbK1ydzvTqOl23J5Bs-MOWeQqOQWHyEkwAiGxKJVUVd_TKz1CvjI6Z7QWp7emnXNKOWVUVx_IjClJi5pJ-pHMpjErtOLqkHzO-ZZSKispPpFDxrQqOa9n5O96wJhDMjj6FCF1sFouHv-Bj7AG40LI4DPcOetxdBbaPSDEFE2KOxefEQwnsLoQxfL_wx_AaOEGd4V1vYt2OoAex8097k-g3Y5gk8sTPQK2OYXt6MIeBvd76wcH_SblqYLvMTtYHJODDkN2X177Ebk--7Fe_Cwur84vFt8vC8OlrAotS6E6w1Up6lpgpbS0mhnNTSlbpJ22znInK4HC1KUUrZFadZ3QmqGsSiaOyLcX3X7bTl-ayfOAoekHf4fDvknom_eb6DfNr7RrONOaq2oSKF4EzJByHlz3xjLaPCfUTAk1bwmJJ7Skhkw</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Translocation of PKCθ in T cells is mediated by a nonconventional, PI3-K– and Vav-dependent pathway, but does not absolutely require phospholipase C</title><source>Alma/SFX Local Collection</source><creator>Villalba, Martin ; Bi, Kun ; Hu, Junru ; Altman, Yoav ; Bushway, Paul ; Reits, Eric ; Neefjes, Jacques ; Baier, Gottfried ; Abraham, Robert T. ; Altman, Amnon</creator><creatorcontrib>Villalba, Martin ; Bi, Kun ; Hu, Junru ; Altman, Yoav ; Bushway, Paul ; Reits, Eric ; Neefjes, Jacques ; Baier, Gottfried ; Abraham, Robert T. ; Altman, Amnon</creatorcontrib><description>PKCθ plays an essential role in activation of mature T cells via stimulation of AP-1 and NF-κB, and is known to selectively translocate to the immunological synapse in antigen-stimulated T cells. Recently, we reported that a Vav/Rac pathway which depends on actin cytoskeleton reorganization mediates selective recruitment of PKCθ to the membrane or cytoskeleton and its catalytic activation by anti-CD3/CD28 costimulation. Because this pathway acted selectively on PKCθ, we addressed here the question of whether the translocation and activation of PKCθ in T cells is regulated by a unique pathway distinct from the conventional mechanism for PKC activation, i.e., PLC-mediated production of DAG. Using three independent approaches, i.e., a selective PLC inhibitor, a PLCγ1-deficient T cell line, or a dominant negative PLCγ1 mutant, we demonstrate that CD3/CD28-induced membrane recruitment and COOH-terminal phosphorylation of PKCθ are largely independent of PLC. In contrast, the same inhibitory strategies blocked the membrane translocation of PKCα. Membrane or lipid raft recruitment of PKCθ (but not PKCα) was absent in T cells treated with phosphatidylinositol 3-kinase (PI3-K) inhibitors or in Vav-deficient T cells, and was enhanced by constitutively active PI3-K. 3-phosphoinositide-dependent kinase-1 (PDK1) also upregulated the membrane translocation of PKCθ, but did not associate with it. These results provide evidence that a nonconventional PI3-K– and Vav-dependent pathway mediates the selective membrane recruitment and, possibly, activation of PKCθ in T cells.</description><identifier>ISSN: 0021-9525</identifier><identifier>EISSN: 1540-8140</identifier><identifier>DOI: 10.1083/jcb.200201097</identifier><identifier>PMID: 11956228</identifier><language>eng</language><publisher>The Rockefeller University Press</publisher><ispartof>The Journal of cell biology, 2002-04, Vol.157 (2), p.253-263</ispartof><rights>Copyright © 2002, The Rockefeller University Press</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2447-94635fc2563883a7594d91c92c64ba0f9ded2e473a3c8643bc495ff3991a47613</citedby><cites>FETCH-LOGICAL-c2447-94635fc2563883a7594d91c92c64ba0f9ded2e473a3c8643bc495ff3991a47613</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids></links><search><creatorcontrib>Villalba, Martin</creatorcontrib><creatorcontrib>Bi, Kun</creatorcontrib><creatorcontrib>Hu, Junru</creatorcontrib><creatorcontrib>Altman, Yoav</creatorcontrib><creatorcontrib>Bushway, Paul</creatorcontrib><creatorcontrib>Reits, Eric</creatorcontrib><creatorcontrib>Neefjes, Jacques</creatorcontrib><creatorcontrib>Baier, Gottfried</creatorcontrib><creatorcontrib>Abraham, Robert T.</creatorcontrib><creatorcontrib>Altman, Amnon</creatorcontrib><title>Translocation of PKCθ in T cells is mediated by a nonconventional, PI3-K– and Vav-dependent pathway, but does not absolutely require phospholipase C</title><title>The Journal of cell biology</title><description>PKCθ plays an essential role in activation of mature T cells via stimulation of AP-1 and NF-κB, and is known to selectively translocate to the immunological synapse in antigen-stimulated T cells. Recently, we reported that a Vav/Rac pathway which depends on actin cytoskeleton reorganization mediates selective recruitment of PKCθ to the membrane or cytoskeleton and its catalytic activation by anti-CD3/CD28 costimulation. Because this pathway acted selectively on PKCθ, we addressed here the question of whether the translocation and activation of PKCθ in T cells is regulated by a unique pathway distinct from the conventional mechanism for PKC activation, i.e., PLC-mediated production of DAG. Using three independent approaches, i.e., a selective PLC inhibitor, a PLCγ1-deficient T cell line, or a dominant negative PLCγ1 mutant, we demonstrate that CD3/CD28-induced membrane recruitment and COOH-terminal phosphorylation of PKCθ are largely independent of PLC. In contrast, the same inhibitory strategies blocked the membrane translocation of PKCα. Membrane or lipid raft recruitment of PKCθ (but not PKCα) was absent in T cells treated with phosphatidylinositol 3-kinase (PI3-K) inhibitors or in Vav-deficient T cells, and was enhanced by constitutively active PI3-K. 3-phosphoinositide-dependent kinase-1 (PDK1) also upregulated the membrane translocation of PKCθ, but did not associate with it. These results provide evidence that a nonconventional PI3-K– and Vav-dependent pathway mediates the selective membrane recruitment and, possibly, activation of PKCθ in T cells.</description><issn>0021-9525</issn><issn>1540-8140</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><recordid>eNpVkU1O3EAQhVtRUJhAltnXAfDQv7Z7EykaBYIGiVkMbK1ydzvTqOl23J5Bs-MOWeQqOQWHyEkwAiGxKJVUVd_TKz1CvjI6Z7QWp7emnXNKOWVUVx_IjClJi5pJ-pHMpjErtOLqkHzO-ZZSKispPpFDxrQqOa9n5O96wJhDMjj6FCF1sFouHv-Bj7AG40LI4DPcOetxdBbaPSDEFE2KOxefEQwnsLoQxfL_wx_AaOEGd4V1vYt2OoAex8097k-g3Y5gk8sTPQK2OYXt6MIeBvd76wcH_SblqYLvMTtYHJODDkN2X177Ebk--7Fe_Cwur84vFt8vC8OlrAotS6E6w1Up6lpgpbS0mhnNTSlbpJ22znInK4HC1KUUrZFadZ3QmqGsSiaOyLcX3X7bTl-ayfOAoekHf4fDvknom_eb6DfNr7RrONOaq2oSKF4EzJByHlz3xjLaPCfUTAk1bwmJJ7Skhkw</recordid><startdate>20020415</startdate><enddate>20020415</enddate><creator>Villalba, Martin</creator><creator>Bi, Kun</creator><creator>Hu, Junru</creator><creator>Altman, Yoav</creator><creator>Bushway, Paul</creator><creator>Reits, Eric</creator><creator>Neefjes, Jacques</creator><creator>Baier, Gottfried</creator><creator>Abraham, Robert T.</creator><creator>Altman, Amnon</creator><general>The Rockefeller University Press</general><scope>AAYXX</scope><scope>CITATION</scope><scope>5PM</scope></search><sort><creationdate>20020415</creationdate><title>Translocation of PKCθ in T cells is mediated by a nonconventional, PI3-K– and Vav-dependent pathway, but does not absolutely require phospholipase C</title><author>Villalba, Martin ; Bi, Kun ; Hu, Junru ; Altman, Yoav ; Bushway, Paul ; Reits, Eric ; Neefjes, Jacques ; Baier, Gottfried ; Abraham, Robert T. ; Altman, Amnon</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2447-94635fc2563883a7594d91c92c64ba0f9ded2e473a3c8643bc495ff3991a47613</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Villalba, Martin</creatorcontrib><creatorcontrib>Bi, Kun</creatorcontrib><creatorcontrib>Hu, Junru</creatorcontrib><creatorcontrib>Altman, Yoav</creatorcontrib><creatorcontrib>Bushway, Paul</creatorcontrib><creatorcontrib>Reits, Eric</creatorcontrib><creatorcontrib>Neefjes, Jacques</creatorcontrib><creatorcontrib>Baier, Gottfried</creatorcontrib><creatorcontrib>Abraham, Robert T.</creatorcontrib><creatorcontrib>Altman, Amnon</creatorcontrib><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of cell biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Villalba, Martin</au><au>Bi, Kun</au><au>Hu, Junru</au><au>Altman, Yoav</au><au>Bushway, Paul</au><au>Reits, Eric</au><au>Neefjes, Jacques</au><au>Baier, Gottfried</au><au>Abraham, Robert T.</au><au>Altman, Amnon</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Translocation of PKCθ in T cells is mediated by a nonconventional, PI3-K– and Vav-dependent pathway, but does not absolutely require phospholipase C</atitle><jtitle>The Journal of cell biology</jtitle><date>2002-04-15</date><risdate>2002</risdate><volume>157</volume><issue>2</issue><spage>253</spage><epage>263</epage><pages>253-263</pages><issn>0021-9525</issn><eissn>1540-8140</eissn><abstract>PKCθ plays an essential role in activation of mature T cells via stimulation of AP-1 and NF-κB, and is known to selectively translocate to the immunological synapse in antigen-stimulated T cells. Recently, we reported that a Vav/Rac pathway which depends on actin cytoskeleton reorganization mediates selective recruitment of PKCθ to the membrane or cytoskeleton and its catalytic activation by anti-CD3/CD28 costimulation. Because this pathway acted selectively on PKCθ, we addressed here the question of whether the translocation and activation of PKCθ in T cells is regulated by a unique pathway distinct from the conventional mechanism for PKC activation, i.e., PLC-mediated production of DAG. Using three independent approaches, i.e., a selective PLC inhibitor, a PLCγ1-deficient T cell line, or a dominant negative PLCγ1 mutant, we demonstrate that CD3/CD28-induced membrane recruitment and COOH-terminal phosphorylation of PKCθ are largely independent of PLC. In contrast, the same inhibitory strategies blocked the membrane translocation of PKCα. Membrane or lipid raft recruitment of PKCθ (but not PKCα) was absent in T cells treated with phosphatidylinositol 3-kinase (PI3-K) inhibitors or in Vav-deficient T cells, and was enhanced by constitutively active PI3-K. 3-phosphoinositide-dependent kinase-1 (PDK1) also upregulated the membrane translocation of PKCθ, but did not associate with it. These results provide evidence that a nonconventional PI3-K– and Vav-dependent pathway mediates the selective membrane recruitment and, possibly, activation of PKCθ in T cells.</abstract><pub>The Rockefeller University Press</pub><pmid>11956228</pmid><doi>10.1083/jcb.200201097</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0021-9525
ispartof The Journal of cell biology, 2002-04, Vol.157 (2), p.253-263
issn 0021-9525
1540-8140
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2199257
source Alma/SFX Local Collection
title Translocation of PKCθ in T cells is mediated by a nonconventional, PI3-K– and Vav-dependent pathway, but does not absolutely require phospholipase C
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-28T22%3A15%3A33IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-pubmedcentral_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Translocation%20of%20PKC%CE%B8%20in%20T%20cells%20is%20mediated%20by%20a%20nonconventional,%20PI3-K%E2%80%93%20and%20Vav-dependent%20pathway,%20but%20does%20not%20absolutely%20require%20phospholipase%20C&rft.jtitle=The%20Journal%20of%20cell%20biology&rft.au=Villalba,%20Martin&rft.date=2002-04-15&rft.volume=157&rft.issue=2&rft.spage=253&rft.epage=263&rft.pages=253-263&rft.issn=0021-9525&rft.eissn=1540-8140&rft_id=info:doi/10.1083/jcb.200201097&rft_dat=%3Cpubmedcentral_cross%3Epubmedcentral_primary_oai_pubmedcentral_nih_gov_2199257%3C/pubmedcentral_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c2447-94635fc2563883a7594d91c92c64ba0f9ded2e473a3c8643bc495ff3991a47613%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/11956228&rfr_iscdi=true