CD69;
T lymphocyte;
cellular activation;
cell surface molecule;
transcription factor;
D O I:
暂无
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
CD69 is the earliest activation antigen expressed on T lymphocytes upon stimulation through the TCR, or with stimuli that mimic TCR triggering. Here we describe that the phorbol ester PMA and a calcium ionophore had a synergistic effect on both CD69 antigen expression and promoter activity in Jurkat cells, that was sensitive to cyclosporin A (CsA). CD69 promoter analysis indicated that the sequence -78 to +16 contained the elements responsible for PMA and PMA plus calcium ionophore induction, as well as CsA inhibition. Mutagenesis of two previously described AP-1 motifs did not affect either the basal or the inducible promoter activities. Electrophoretic mobility shift assays allowed the identification of three novel inducible complexes composed by Egr-1/Egr-3, Egr-1, and ATF-3/Fos. Mutation of each sequence resulted in a partial reduction of the basal promoter activity, whereas the inducibility by PMA plus calcium ionophore remained almost unaffected. It was necessary to combine at least two mutations to obtain a significative or complete reduction of the response to the mitogenic stimulus. These results indicate that the inducible expression of CD69 gene by mitogenic signals is regulated by multiple cis-acting elements and by the interplay of transcription factors of the AP-1, EGR and ATF/CREB families.
机构:
UNIV CALIF SAN FRANCISCO, GLADSTONE FDN LABS CARDIOVASC DIS, SAN FRANCISCO, CA 94143 USAUNIV CALIF SAN FRANCISCO, GLADSTONE FDN LABS CARDIOVASC DIS, SAN FRANCISCO, CA 94143 USA
PAIK, YK
CHANG, DJ
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机构:
UNIV CALIF SAN FRANCISCO, GLADSTONE FDN LABS CARDIOVASC DIS, SAN FRANCISCO, CA 94143 USAUNIV CALIF SAN FRANCISCO, GLADSTONE FDN LABS CARDIOVASC DIS, SAN FRANCISCO, CA 94143 USA
CHANG, DJ
TAYLOR, JM
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h-index: 0
机构:
UNIV CALIF SAN FRANCISCO, GLADSTONE FDN LABS CARDIOVASC DIS, SAN FRANCISCO, CA 94143 USAUNIV CALIF SAN FRANCISCO, GLADSTONE FDN LABS CARDIOVASC DIS, SAN FRANCISCO, CA 94143 USA
机构:
UNIV TEXAS,MD ANDERSON CANCER CTR,DEPT GASTROINTESTINAL MED ONCOL & DIGEST DIS,DIV MED,HOUSTON,TX 77030UNIV TEXAS,MD ANDERSON CANCER CTR,DEPT GASTROINTESTINAL MED ONCOL & DIGEST DIS,DIV MED,HOUSTON,TX 77030
Jones, DV
Wu, E
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h-index: 0
机构:
UNIV TEXAS,MD ANDERSON CANCER CTR,DEPT GASTROINTESTINAL MED ONCOL & DIGEST DIS,DIV MED,HOUSTON,TX 77030UNIV TEXAS,MD ANDERSON CANCER CTR,DEPT GASTROINTESTINAL MED ONCOL & DIGEST DIS,DIV MED,HOUSTON,TX 77030
Wu, E
Manire, M
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h-index: 0
机构:
UNIV TEXAS,MD ANDERSON CANCER CTR,DEPT GASTROINTESTINAL MED ONCOL & DIGEST DIS,DIV MED,HOUSTON,TX 77030UNIV TEXAS,MD ANDERSON CANCER CTR,DEPT GASTROINTESTINAL MED ONCOL & DIGEST DIS,DIV MED,HOUSTON,TX 77030
Manire, M
Frazier, ML
论文数: 0引用数: 0
h-index: 0
机构:
UNIV TEXAS,MD ANDERSON CANCER CTR,DEPT GASTROINTESTINAL MED ONCOL & DIGEST DIS,DIV MED,HOUSTON,TX 77030UNIV TEXAS,MD ANDERSON CANCER CTR,DEPT GASTROINTESTINAL MED ONCOL & DIGEST DIS,DIV MED,HOUSTON,TX 77030