Differential requirement for protein tyrosine kinase Fyn in the functional activation of antigen-specific T lymphocyte clones through the TCR or Thy-1
The protein tyrosine kinase Fyn has been shown to be involved in signal transduction through the TCR and the glycosyl-phosphatidylinositol-linked surface molecule Thy-1 expressed on T cells. In this study, we examine the requirement for Fyn expression in signaling through the TCR or Thy-1 using a pa...
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Veröffentlicht in: | The Journal of immunology (1950) 1995-05, Vol.154 (9), p.4363-4370 |
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container_title | The Journal of immunology (1950) |
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creator | Lancki, DW Qian, D Fields, P Gajewski, T Fitch, FW |
description | The protein tyrosine kinase Fyn has been shown to be involved in signal transduction through the TCR and the glycosyl-phosphatidylinositol-linked surface molecule Thy-1 expressed on T cells. In this study, we examine the requirement for Fyn expression in signaling through the TCR or Thy-1 using a panel of Ag-specific T cell clones derived from fyn-/- mutant mice. These clones do not express normal Fyn protein, as measured by immune-complex kinase reaction using anti-Fyn Ab. Stimulation through the TCR, either by APC bearing relevant Ag or by immobilized anti-CD3 mAb, resulted in comparable levels of proliferation, lymphokine production, and cytolysis by clones from both wild-type and fyn-/- mice. In contrast, stimulation through Thy-1, using soluble (or cross-linked) anti-Thy-1 mAb, was deficient, as measured by these responses. Thus, Fyn expression is selectively required for functional activation through Thy-1 in these T cell clones. |
doi_str_mv | 10.4049/jimmunol.154.9.4363 |
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In this study, we examine the requirement for Fyn expression in signaling through the TCR or Thy-1 using a panel of Ag-specific T cell clones derived from fyn-/- mutant mice. These clones do not express normal Fyn protein, as measured by immune-complex kinase reaction using anti-Fyn Ab. Stimulation through the TCR, either by APC bearing relevant Ag or by immobilized anti-CD3 mAb, resulted in comparable levels of proliferation, lymphokine production, and cytolysis by clones from both wild-type and fyn-/- mice. In contrast, stimulation through Thy-1, using soluble (or cross-linked) anti-Thy-1 mAb, was deficient, as measured by these responses. Thus, Fyn expression is selectively required for functional activation through Thy-1 in these T cell clones.</description><identifier>ISSN: 0022-1767</identifier><identifier>EISSN: 1550-6606</identifier><identifier>DOI: 10.4049/jimmunol.154.9.4363</identifier><identifier>PMID: 7722293</identifier><language>eng</language><publisher>United States: Am Assoc Immnol</publisher><subject>Animals ; Cell Line ; Cytotoxicity Tests, Immunologic ; Flow Cytometry ; Lymphocyte Activation - immunology ; Male ; Mice ; Mice, Inbred C57BL ; Mice, Inbred DBA ; Protein-Tyrosine Kinases - immunology ; Proto-Oncogene Proteins - immunology ; Proto-Oncogene Proteins c-fyn ; Receptors, Antigen, T-Cell - immunology ; Signal Transduction - immunology ; T-Lymphocytes - immunology ; Th1 Cells - immunology ; Thy-1 Antigens - immunology</subject><ispartof>The Journal of immunology (1950), 1995-05, Vol.154 (9), p.4363-4370</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c363t-6c0da273c4808b4c9cb727c879bd9e8084b8355622ac669bc4c8cab06e4fe4f63</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7722293$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lancki, DW</creatorcontrib><creatorcontrib>Qian, D</creatorcontrib><creatorcontrib>Fields, P</creatorcontrib><creatorcontrib>Gajewski, T</creatorcontrib><creatorcontrib>Fitch, FW</creatorcontrib><title>Differential requirement for protein tyrosine kinase Fyn in the functional activation of antigen-specific T lymphocyte clones through the TCR or Thy-1</title><title>The Journal of immunology (1950)</title><addtitle>J Immunol</addtitle><description>The protein tyrosine kinase Fyn has been shown to be involved in signal transduction through the TCR and the glycosyl-phosphatidylinositol-linked surface molecule Thy-1 expressed on T cells. In this study, we examine the requirement for Fyn expression in signaling through the TCR or Thy-1 using a panel of Ag-specific T cell clones derived from fyn-/- mutant mice. These clones do not express normal Fyn protein, as measured by immune-complex kinase reaction using anti-Fyn Ab. Stimulation through the TCR, either by APC bearing relevant Ag or by immobilized anti-CD3 mAb, resulted in comparable levels of proliferation, lymphokine production, and cytolysis by clones from both wild-type and fyn-/- mice. In contrast, stimulation through Thy-1, using soluble (or cross-linked) anti-Thy-1 mAb, was deficient, as measured by these responses. Thus, Fyn expression is selectively required for functional activation through Thy-1 in these T cell clones.</description><subject>Animals</subject><subject>Cell Line</subject><subject>Cytotoxicity Tests, Immunologic</subject><subject>Flow Cytometry</subject><subject>Lymphocyte Activation - immunology</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Inbred DBA</subject><subject>Protein-Tyrosine Kinases - immunology</subject><subject>Proto-Oncogene Proteins - immunology</subject><subject>Proto-Oncogene Proteins c-fyn</subject><subject>Receptors, Antigen, T-Cell - immunology</subject><subject>Signal Transduction - immunology</subject><subject>T-Lymphocytes - immunology</subject><subject>Th1 Cells - immunology</subject><subject>Thy-1 Antigens - immunology</subject><issn>0022-1767</issn><issn>1550-6606</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpNUdGO1CAUJUazzq5-gTHhSZ86AqXQPprRXU02MTHjM6HMZcpKYRbanfRH_F4ZZzQmJHDvPeeQew5CbyhZc8K7Dw9uHOcQ_Zo2fN2teS3qZ2hFm4ZUQhDxHK0IYayiUsiX6DrnB0KIIIxfoSspGWNdvUK_PjlrIUGYnPY4wePsEoylxDYmfEhxAhfwtKSYXQD80wWdAd8uAZ_aA2A7BzO5GApbl8eTPhU4WqyL5B5ClQ9gnHUGb7FfxsMQzTIBNj4GyEUhxXk__FHabr7j8ud2WCr6Cr2w2md4fblv0I_bz9vNl-r-293Xzcf7ypRlp0oYstNM1oa3pO256UwvmTSt7PpdB6XH-7ZuGsGYNkJ0veGmNbonArgtR9Q36N1Zt2z6OEOe1OiyAe91gDhnRYUUlDR1AdZnoClO5ARWHZIbdVoUJeqUhvqbhippqE6d0iistxf5uR9h949zsb_M35_ng9sPx-K8yqP2vqCpOh6P_yn9Bg4umTc</recordid><startdate>19950501</startdate><enddate>19950501</enddate><creator>Lancki, DW</creator><creator>Qian, D</creator><creator>Fields, P</creator><creator>Gajewski, T</creator><creator>Fitch, FW</creator><general>Am Assoc Immnol</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>7T5</scope><scope>H94</scope></search><sort><creationdate>19950501</creationdate><title>Differential requirement for protein tyrosine kinase Fyn in the functional activation of antigen-specific T lymphocyte clones through the TCR or Thy-1</title><author>Lancki, DW ; Qian, D ; Fields, P ; Gajewski, T ; Fitch, FW</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c363t-6c0da273c4808b4c9cb727c879bd9e8084b8355622ac669bc4c8cab06e4fe4f63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>Animals</topic><topic>Cell Line</topic><topic>Cytotoxicity Tests, Immunologic</topic><topic>Flow Cytometry</topic><topic>Lymphocyte Activation - immunology</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Inbred DBA</topic><topic>Protein-Tyrosine Kinases - immunology</topic><topic>Proto-Oncogene Proteins - immunology</topic><topic>Proto-Oncogene Proteins c-fyn</topic><topic>Receptors, Antigen, T-Cell - immunology</topic><topic>Signal Transduction - immunology</topic><topic>T-Lymphocytes - immunology</topic><topic>Th1 Cells - immunology</topic><topic>Thy-1 Antigens - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lancki, DW</creatorcontrib><creatorcontrib>Qian, D</creatorcontrib><creatorcontrib>Fields, P</creatorcontrib><creatorcontrib>Gajewski, T</creatorcontrib><creatorcontrib>Fitch, FW</creatorcontrib><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><jtitle>The Journal of immunology (1950)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lancki, DW</au><au>Qian, D</au><au>Fields, P</au><au>Gajewski, T</au><au>Fitch, FW</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Differential requirement for protein tyrosine kinase Fyn in the functional activation of antigen-specific T lymphocyte clones through the TCR or Thy-1</atitle><jtitle>The Journal of immunology (1950)</jtitle><addtitle>J Immunol</addtitle><date>1995-05-01</date><risdate>1995</risdate><volume>154</volume><issue>9</issue><spage>4363</spage><epage>4370</epage><pages>4363-4370</pages><issn>0022-1767</issn><eissn>1550-6606</eissn><abstract>The protein tyrosine kinase Fyn has been shown to be involved in signal transduction through the TCR and the glycosyl-phosphatidylinositol-linked surface molecule Thy-1 expressed on T cells. In this study, we examine the requirement for Fyn expression in signaling through the TCR or Thy-1 using a panel of Ag-specific T cell clones derived from fyn-/- mutant mice. These clones do not express normal Fyn protein, as measured by immune-complex kinase reaction using anti-Fyn Ab. Stimulation through the TCR, either by APC bearing relevant Ag or by immobilized anti-CD3 mAb, resulted in comparable levels of proliferation, lymphokine production, and cytolysis by clones from both wild-type and fyn-/- mice. In contrast, stimulation through Thy-1, using soluble (or cross-linked) anti-Thy-1 mAb, was deficient, as measured by these responses. Thus, Fyn expression is selectively required for functional activation through Thy-1 in these T cell clones.</abstract><cop>United States</cop><pub>Am Assoc Immnol</pub><pmid>7722293</pmid><doi>10.4049/jimmunol.154.9.4363</doi><tpages>8</tpages></addata></record> |
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subjects | Animals Cell Line Cytotoxicity Tests, Immunologic Flow Cytometry Lymphocyte Activation - immunology Male Mice Mice, Inbred C57BL Mice, Inbred DBA Protein-Tyrosine Kinases - immunology Proto-Oncogene Proteins - immunology Proto-Oncogene Proteins c-fyn Receptors, Antigen, T-Cell - immunology Signal Transduction - immunology T-Lymphocytes - immunology Th1 Cells - immunology Thy-1 Antigens - immunology |
title | Differential requirement for protein tyrosine kinase Fyn in the functional activation of antigen-specific T lymphocyte clones through the TCR or Thy-1 |
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