Reciprocal expression of co‐stimulatory molecules, B7‐1 and B7‐2, on murine T cells following activation
The co‐stimulatory B7 molecules (B7‐1 and B7‐2) are expressed on professional antigen‐presenting cells in mice. In this study, we demonstrate that B7‐1 (CD80) and B7‐2 (CD86) are also expressed on murine T cells in the absence of major histocompatibility complex class II molecules. The temporal expr...
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Veröffentlicht in: | European journal of immunology 1995-01, Vol.25 (1), p.207-211 |
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creator | Das, Mercy R. Prabhu Zamvil, Scott S. Borriello, Frank Weiner, Howard L. Sharpe, Arlene H. Kuchroo, Vijay K. |
description | The co‐stimulatory B7 molecules (B7‐1 and B7‐2) are expressed on professional antigen‐presenting cells in mice. In this study, we demonstrate that B7‐1 (CD80) and B7‐2 (CD86) are also expressed on murine T cells in the absence of major histocompatibility complex class II molecules. The temporal expression of these two molecules on T cells varies with the state of activation where resting T cells express B7‐2 but show little or no expression of B7‐1. Following activation, B7‐2 expression is down‐regulated and there is a concomitant increase in the expression of B7‐1 on the cell surface which peaks at about 72 h. Thus these two co‐stimulatory molecules are reciprocally expressed on the T cell surface. This pattern of expression of B7‐1 and B7‐2 on T cells suggests that these two molecules may have different roles in the generation and regulation of immune responses. |
doi_str_mv | 10.1002/eji.1830250134 |
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Prabhu ; Zamvil, Scott S. ; Borriello, Frank ; Weiner, Howard L. ; Sharpe, Arlene H. ; Kuchroo, Vijay K.</creator><creatorcontrib>Das, Mercy R. Prabhu ; Zamvil, Scott S. ; Borriello, Frank ; Weiner, Howard L. ; Sharpe, Arlene H. ; Kuchroo, Vijay K.</creatorcontrib><description>The co‐stimulatory B7 molecules (B7‐1 and B7‐2) are expressed on professional antigen‐presenting cells in mice. In this study, we demonstrate that B7‐1 (CD80) and B7‐2 (CD86) are also expressed on murine T cells in the absence of major histocompatibility complex class II molecules. The temporal expression of these two molecules on T cells varies with the state of activation where resting T cells express B7‐2 but show little or no expression of B7‐1. Following activation, B7‐2 expression is down‐regulated and there is a concomitant increase in the expression of B7‐1 on the cell surface which peaks at about 72 h. Thus these two co‐stimulatory molecules are reciprocally expressed on the T cell surface. This pattern of expression of B7‐1 and B7‐2 on T cells suggests that these two molecules may have different roles in the generation and regulation of immune responses.</description><identifier>ISSN: 0014-2980</identifier><identifier>EISSN: 1521-4141</identifier><identifier>DOI: 10.1002/eji.1830250134</identifier><identifier>PMID: 7531145</identifier><language>eng</language><publisher>Weinheim: WILEY‐VCH Verlag GmbH</publisher><subject>Amino Acid Sequence ; Animals ; Antibodies, Monoclonal - immunology ; Antigens, CD ; B7-1 Antigen - biosynthesis ; B7-2 Antigen ; B7‐1 ; B7‐2 ; Clone Cells ; Co‐stimulatory molecules ; Female ; Flow Cytometry ; Fluorescent Antibody Technique ; Lymphocyte Activation - immunology ; Membrane Glycoproteins - biosynthesis ; Mice ; Mice, Inbred Strains ; Molecular Sequence Data ; Murine T cells ; Myelin Basic Protein - immunology ; T-Lymphocytes - immunology</subject><ispartof>European journal of immunology, 1995-01, Vol.25 (1), p.207-211</ispartof><rights>Copyright © 1995 WILEY‐VCH Verlag GmbH & Co. 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Prabhu</creatorcontrib><creatorcontrib>Zamvil, Scott S.</creatorcontrib><creatorcontrib>Borriello, Frank</creatorcontrib><creatorcontrib>Weiner, Howard L.</creatorcontrib><creatorcontrib>Sharpe, Arlene H.</creatorcontrib><creatorcontrib>Kuchroo, Vijay K.</creatorcontrib><title>Reciprocal expression of co‐stimulatory molecules, B7‐1 and B7‐2, on murine T cells following activation</title><title>European journal of immunology</title><addtitle>Eur J Immunol</addtitle><description>The co‐stimulatory B7 molecules (B7‐1 and B7‐2) are expressed on professional antigen‐presenting cells in mice. In this study, we demonstrate that B7‐1 (CD80) and B7‐2 (CD86) are also expressed on murine T cells in the absence of major histocompatibility complex class II molecules. The temporal expression of these two molecules on T cells varies with the state of activation where resting T cells express B7‐2 but show little or no expression of B7‐1. Following activation, B7‐2 expression is down‐regulated and there is a concomitant increase in the expression of B7‐1 on the cell surface which peaks at about 72 h. Thus these two co‐stimulatory molecules are reciprocally expressed on the T cell surface. This pattern of expression of B7‐1 and B7‐2 on T cells suggests that these two molecules may have different roles in the generation and regulation of immune responses.</description><subject>Amino Acid Sequence</subject><subject>Animals</subject><subject>Antibodies, Monoclonal - immunology</subject><subject>Antigens, CD</subject><subject>B7-1 Antigen - biosynthesis</subject><subject>B7-2 Antigen</subject><subject>B7‐1</subject><subject>B7‐2</subject><subject>Clone Cells</subject><subject>Co‐stimulatory molecules</subject><subject>Female</subject><subject>Flow Cytometry</subject><subject>Fluorescent Antibody Technique</subject><subject>Lymphocyte Activation - immunology</subject><subject>Membrane Glycoproteins - biosynthesis</subject><subject>Mice</subject><subject>Mice, Inbred Strains</subject><subject>Molecular Sequence Data</subject><subject>Murine T cells</subject><subject>Myelin Basic Protein - immunology</subject><subject>T-Lymphocytes - immunology</subject><issn>0014-2980</issn><issn>1521-4141</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1LxDAQhoMouq5evQk5ebJrpvloe1TxE0GQ9VzS7FQiabM2reve_An-Rn-JkV3Um6cZeN95mJmXkANgE2AsPcFnO4Gcs1Qy4GKDjECmkAgQsElGjIFI0iJnO2Q3hGfGWKFksU22M8kBhByR9gGNnXfeaEfxbd5hCNa31NfU-M_3j9DbZnC6992SNt6hGRyGY3qWRQ2obmerNj2mcagZOtsinVKDzgVae-f8wrZPVJvevuo-gvfIVq1dwP11HZPHy4vp-XVyd391c356lxgOUiQVxMpVxRBzI2ShRJFlUqjMpKpg6UyqSitglcqxqut4pcKKC16bHPJUKeRjcrTixtNeBgx92djwvZZu0Q-hzDLgoAr5rxFUFo0sj8bJymg6H0KHdTnvbKO7ZQms_E6ijEmUv0nEgcM1eaganP3Y16-PerHSF9bh8h9aeXF784f9BR8xlkY</recordid><startdate>199501</startdate><enddate>199501</enddate><creator>Das, Mercy R. Prabhu</creator><creator>Zamvil, Scott S.</creator><creator>Borriello, Frank</creator><creator>Weiner, Howard L.</creator><creator>Sharpe, Arlene H.</creator><creator>Kuchroo, Vijay K.</creator><general>WILEY‐VCH Verlag GmbH</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><scope>7X8</scope></search><sort><creationdate>199501</creationdate><title>Reciprocal expression of co‐stimulatory molecules, B7‐1 and B7‐2, on murine T cells following activation</title><author>Das, Mercy R. Prabhu ; Zamvil, Scott S. ; Borriello, Frank ; Weiner, Howard L. ; Sharpe, Arlene H. ; Kuchroo, Vijay K.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3154-b1c3136b0ee8c459649775467c26902d56ba610b68ebff0016eb343fc818266e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>Amino Acid Sequence</topic><topic>Animals</topic><topic>Antibodies, Monoclonal - immunology</topic><topic>Antigens, CD</topic><topic>B7-1 Antigen - biosynthesis</topic><topic>B7-2 Antigen</topic><topic>B7‐1</topic><topic>B7‐2</topic><topic>Clone Cells</topic><topic>Co‐stimulatory molecules</topic><topic>Female</topic><topic>Flow Cytometry</topic><topic>Fluorescent Antibody Technique</topic><topic>Lymphocyte Activation - immunology</topic><topic>Membrane Glycoproteins - biosynthesis</topic><topic>Mice</topic><topic>Mice, Inbred Strains</topic><topic>Molecular Sequence Data</topic><topic>Murine T cells</topic><topic>Myelin Basic Protein - immunology</topic><topic>T-Lymphocytes - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Das, Mercy R. Prabhu</creatorcontrib><creatorcontrib>Zamvil, Scott S.</creatorcontrib><creatorcontrib>Borriello, Frank</creatorcontrib><creatorcontrib>Weiner, Howard L.</creatorcontrib><creatorcontrib>Sharpe, Arlene H.</creatorcontrib><creatorcontrib>Kuchroo, Vijay K.</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><collection>MEDLINE - Academic</collection><jtitle>European journal of immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Das, Mercy R. Prabhu</au><au>Zamvil, Scott S.</au><au>Borriello, Frank</au><au>Weiner, Howard L.</au><au>Sharpe, Arlene H.</au><au>Kuchroo, Vijay K.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Reciprocal expression of co‐stimulatory molecules, B7‐1 and B7‐2, on murine T cells following activation</atitle><jtitle>European journal of immunology</jtitle><addtitle>Eur J Immunol</addtitle><date>1995-01</date><risdate>1995</risdate><volume>25</volume><issue>1</issue><spage>207</spage><epage>211</epage><pages>207-211</pages><issn>0014-2980</issn><eissn>1521-4141</eissn><abstract>The co‐stimulatory B7 molecules (B7‐1 and B7‐2) are expressed on professional antigen‐presenting cells in mice. In this study, we demonstrate that B7‐1 (CD80) and B7‐2 (CD86) are also expressed on murine T cells in the absence of major histocompatibility complex class II molecules. The temporal expression of these two molecules on T cells varies with the state of activation where resting T cells express B7‐2 but show little or no expression of B7‐1. Following activation, B7‐2 expression is down‐regulated and there is a concomitant increase in the expression of B7‐1 on the cell surface which peaks at about 72 h. Thus these two co‐stimulatory molecules are reciprocally expressed on the T cell surface. This pattern of expression of B7‐1 and B7‐2 on T cells suggests that these two molecules may have different roles in the generation and regulation of immune responses.</abstract><cop>Weinheim</cop><pub>WILEY‐VCH Verlag GmbH</pub><pmid>7531145</pmid><doi>10.1002/eji.1830250134</doi><tpages>5</tpages></addata></record> |
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subjects | Amino Acid Sequence Animals Antibodies, Monoclonal - immunology Antigens, CD B7-1 Antigen - biosynthesis B7-2 Antigen B7‐1 B7‐2 Clone Cells Co‐stimulatory molecules Female Flow Cytometry Fluorescent Antibody Technique Lymphocyte Activation - immunology Membrane Glycoproteins - biosynthesis Mice Mice, Inbred Strains Molecular Sequence Data Murine T cells Myelin Basic Protein - immunology T-Lymphocytes - immunology |
title | Reciprocal expression of co‐stimulatory molecules, B7‐1 and B7‐2, on murine T cells following activation |
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