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. 1993 Sep 1;178(3):901-8.
doi: 10.1084/jem.178.3.901.

Positive selection of V beta 8+ CD4-8- thymocytes by class I molecules expressed by hematopoietic cells

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Positive selection of V beta 8+ CD4-8- thymocytes by class I molecules expressed by hematopoietic cells

M Bix et al. J Exp Med. .

Abstract

A small subset of T cells of mature phenotype express the alpha/beta T cell receptor, but not CD4 and CD8 coreceptors (alpha/beta double-negative [DN] cells). The repertoire of V beta usage of alpha/beta DN cells is strongly biased towards V beta 8 expression, suggesting that the formation of the population is subject to selection. We now report that deficiency of class I expression leads to a strongly depressed frequency of V beta 8+ DN cells, but has little effect on V beta 8- DN cells. Studies of hematopoietic chimeras between class I+ and class I- mice demonstrated that expression of class I molecules by hematopoietic cells is necessary and sufficient for selection of most V beta 8 DN cells. The lack of a role for class I expression by thymic epithelial cells suggests that the mechanism of selection of these cells by class I differs significantly from the mechanism of selection of conventional T cells. Models to explain the selection of these cells as well as their possible function in vivo are discussed.

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    1. J Immunol. 1985 Jun;134(6):3994-4000 - PubMed
    1. Cell. 1992 Jul 24;70(2):215-23 - PubMed
    1. Nature. 1986 May 15-21;321(6067):219-26 - PubMed
    1. Nature. 1986 Dec 18-31;324(6098):679-82 - PubMed
    1. Cell. 1987 Apr 24;49(2):273-80 - PubMed

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