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Stochastic coreceptor shut-off is restricted to the CD4 lineage maturation pathway

Kinetics of mature T cell generation in the thymus of normal or major histocompatibility complex (MHC) class I- or II-deficient mice were studied by the bromodeoxyuridine pulse labeling method. As previously described, the early activation and final maturation phases were found to be synchronous for...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1995
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2191984/
https://www.ncbi.nlm.nih.gov/pubmed/7722442
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description Kinetics of mature T cell generation in the thymus of normal or major histocompatibility complex (MHC) class I- or II-deficient mice were studied by the bromodeoxyuridine pulse labeling method. As previously described, the early activation and final maturation phases were found to be synchronous for the two T cell lineages, but CD4+8- cells were generated faster than CD4-8+ cells in MHC class I- and II-deficient mice, respectively. CD8 downregulation started on day 2 after cell proliferation even in the absence of MHC class II expression. CD8 downregulation thus appears to be stochastic at its beginning. By contrast, CD4 shut-off was found totally instructive, as the generation of CD4lo8+ cells with a high TCR density was not observed in class I- deficient mice. The analysis of the V beta 14 TCR frequencies in CD4/8 subsets in normal and MHC-deficient mice confirmed that CD4 and CD8 generation pathways are not symmetrical. These findings show that commitment towards the CD4+8- or CD4-8+ phenotype is controlled at the CD8lo step for the former and at the CD4+8+ double-positive stage for the latter.
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spelling pubmed-21919842008-04-16 Stochastic coreceptor shut-off is restricted to the CD4 lineage maturation pathway J Exp Med Articles Kinetics of mature T cell generation in the thymus of normal or major histocompatibility complex (MHC) class I- or II-deficient mice were studied by the bromodeoxyuridine pulse labeling method. As previously described, the early activation and final maturation phases were found to be synchronous for the two T cell lineages, but CD4+8- cells were generated faster than CD4-8+ cells in MHC class I- and II-deficient mice, respectively. CD8 downregulation started on day 2 after cell proliferation even in the absence of MHC class II expression. CD8 downregulation thus appears to be stochastic at its beginning. By contrast, CD4 shut-off was found totally instructive, as the generation of CD4lo8+ cells with a high TCR density was not observed in class I- deficient mice. The analysis of the V beta 14 TCR frequencies in CD4/8 subsets in normal and MHC-deficient mice confirmed that CD4 and CD8 generation pathways are not symmetrical. These findings show that commitment towards the CD4+8- or CD4-8+ phenotype is controlled at the CD8lo step for the former and at the CD4+8+ double-positive stage for the latter. The Rockefeller University Press 1995-05-01 /pmc/articles/PMC2191984/ /pubmed/7722442 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Articles
Stochastic coreceptor shut-off is restricted to the CD4 lineage maturation pathway
title Stochastic coreceptor shut-off is restricted to the CD4 lineage maturation pathway
title_full Stochastic coreceptor shut-off is restricted to the CD4 lineage maturation pathway
title_fullStr Stochastic coreceptor shut-off is restricted to the CD4 lineage maturation pathway
title_full_unstemmed Stochastic coreceptor shut-off is restricted to the CD4 lineage maturation pathway
title_short Stochastic coreceptor shut-off is restricted to the CD4 lineage maturation pathway
title_sort stochastic coreceptor shut-off is restricted to the cd4 lineage maturation pathway
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2191984/
https://www.ncbi.nlm.nih.gov/pubmed/7722442