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Immunity ; 9(4): 497-508, 1998 Oct.
Article in English | MEDLINE | ID: mdl-9806636

ABSTRACT

CD4 and CD8 are crucial for the development and function of T cells. An intergenic deoxyribonuclease I hypersensitive site region (cluster CIII) directs expression in mature CD8 T cells only. Here, we show that two further independent regions from the CD8 gene locus in conjunction with cluster CIII restore transgene expression in appropriate immature thymocytes. Deletion of two of the intergenic cluster CIII DNaseI-HSS in homozygous mutant mice affects expression of CD8alphaalpha homodimers on intraepithelial T cells (IEL), particularly on the gammadeltaTCR+ subset. Surprisingly, none of the thymocyte or peripheral alphabetaTCR T cell subsets are affected by this mutation, indicating hierarchical activation of these elements within the different T cell subsets.


Subject(s)
CD8 Antigens/genetics , T-Lymphocyte Subsets/immunology , Alleles , Animals , Cell Differentiation , Chromosome Mapping , DNA/genetics , Deoxyribonuclease I , Female , Gene Expression Regulation, Developmental , Genes, Reporter , Male , Mice , Mice, Knockout , Mice, Mutant Strains , Mice, Transgenic , Mutation , Receptors, Antigen, T-Cell, alpha-beta/genetics , Receptors, Antigen, T-Cell, gamma-delta/genetics , Sequence Deletion , T-Lymphocyte Subsets/cytology
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