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Science 13 August 1993:
Vol. 261. no. 5123, pp. 911 - 915
DOI: 10.1126/science.8102208
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Articles

Science, Vol 261, Issue 5123, 911-915
Copyright © 1993 by American Association for the Advancement of Science

articles

Development of mature CD8+ thymocytes: selection rather than instruction?

JP van Meerwijk and RN Germain

Lymphocyte Biology Section, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892.

The role of major histocompatibility complex (MHC) molecules in T cell differentiation was investigated by comparison of thymocyte subpopulations in wild-type mice and beta 2-microglobulin (beta 2M) mutant mice deficient in MHC class I expression and mature CD8+ cells. On the basis of surface markers, glucocorticoid resistance, in vitro differentiation capacity, and absence in beta 2 M-l- mice, CD4intermediateCD8hi cells with high expression of alpha beta T cell receptor (TCR alpha beta) were identified as having been positively selected by MHC class I for development into mature CD8+ T cells. Activated CD4intCD8hi cells bearing intermediate rather than high amounts of TCR were present in both wild-type and beta 2M-l- animals. These data suggest that recognition of MHC class I molecules is required for full maturation to CD8+ T cells, but not for receptor-initiated commitment to the CD8+ lineage, consistent with a stochastic (selection) model of thymocyte development.


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Peripheral T Cell Survival Requires Continual Ligation of the T Cell Receptor to Major Histocompatibility Complex-Encoded Molecules.
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A subset of CD4+ thymocytes selected by MHC class I molecules.
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Science. ISSN 0036-8075 (print), 1095-9203 (online)