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
Hauptverfasser: Das, Mercy R. Prabhu, Zamvil, Scott S., Borriello, Frank, Weiner, Howard L., Sharpe, Arlene H., Kuchroo, Vijay K.
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container_end_page 211
container_issue 1
container_start_page 207
container_title European journal of immunology
container_volume 25
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. 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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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source MEDLINE; Wiley Online Library Journals Frontfile Complete
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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