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Participation of CD4 coreceptor molecules in T-cell repertoire selection.

作者信息

Teh H S, Garvin A M, Forbush K A, Carlow D A, Davis C B, Littman D R, Perlmutter R M

机构信息

Department of Microbiology, University of British Columbia, Vancouver, Canada.

出版信息

Nature. 1991 Jan 17;349(6306):241-3. doi: 10.1038/349241a0.

DOI:10.1038/349241a0
PMID:1824796
Abstract

During thymocyte development, progenitor cells bearing both CD4 and CD8 coreceptor molecules mature into functional T lymphocytes that express these proteins in a mutually exclusive way. Although T-cell specificity is determined primarily by the structure of the T-cell antigen receptor (TCR) heterodimer, a developmentally regulated process acts to ensure that cells bearing class II-restricted TCRs are CD4+ and those bearing class I-restricted TCRs express only CD8. To investigate this maturation process, we have engineered transgenic mice in which CD4 is expressed in all thymocyte subsets and in all peripheral T cells. Peripheral CD4+8+ T lymphocytes from these mice react with both class I and class II alloantigens. Moreover, expression of the CD4 transgene disrupts the positive selection of doubly transgenic thymocytes bearing a class I-restricted TCR specific for the male (H-Y) antigen. Hence the CD4 coreceptor participates directly in T-cell repertoire selection.

摘要

相似文献

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