ACTIVATION SIGNAL INDUCES THE EXPRESSION OF B-CELL-SPECIFIC CD45R EPITOPE (6B2) ON MURINE T-CELLS

被引:27
作者
WATANABE, Y
AKAIKE, T
机构
[1] Department of Biomolecular Engineering, Tokyo Institute of Technology, Yokohama
关键词
D O I
10.1111/j.1365-3083.1994.tb03395.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
T lymphocytes express multiple forms of the leukocyte-common antigen CD45, transcribed by alternative usage of leukocyte-common antigen exon 4-6. The various isoforms of CD45R expressed differentially on T cells are involved in different stages of development and activation. The monoclonal antibody (MoAb) RA3-6B2 is established as a B cell-type isoform (B220)-specific marker. However, it reacts with certain activated T cells although the relationship between 6B2 expression and T-cell activation is unclear. We have examined the 6B2 expression on activated T cells and found that concanavalin A, anti-CD3 antibody and staphylococcal enterotoxin B (SEB) induced 6B2 expression on T cells. The expression was found on both CD4(+) and CD8(+) T cells and also was induced by SEB in vivo predominantly on CD8(+) T cells. The 6B2(+) T cells are IL-2R(+) and blasted cells according to flow cytometry analysis. Therefore, the 6B2(+) T cells are supposed to be in an activated stage. Enzymatic analysis demonstrated that trypsin treatment decreased the 6B2 expression, whereas neuraminidase increased the intensity on activated T cells. Neither endo-D or endo-H have any effect on the expression and there are no differences, in the results of immunoprecipitation and RT-PCR analysis, between control T cells and activated T cells. Taken together, the 6B2 epitope is presumed to be the product of CD45R modification and is expressed on activated T cells. These results illustrate a novel classification of a T-cell subpopulation bearing a 6B2 epitope.
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页码:419 / 425
页数:7
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