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Identification of a Committed T Cell Precursor Population in Adult Human Peripheral Blood

Here, we report data concerning the discovery in adult human peripheral blood of a precursor cell population able to differentiate into CD4(+)CD3(+)αβ(+) mature T cells. These cells, which represent 0.1–0.5% of total peripheral blood mononuclear cells (PBMC), express substantial levels of CD4, but l...

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Autores principales: Bruno, Ludovica, Res, Pieter, Dessing, Mark, Cella, Marina, Spits, Hergen
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1997
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2196171/
https://www.ncbi.nlm.nih.gov/pubmed/9120393
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author Bruno, Ludovica
Res, Pieter
Dessing, Mark
Cella, Marina
Spits, Hergen
author_facet Bruno, Ludovica
Res, Pieter
Dessing, Mark
Cella, Marina
Spits, Hergen
author_sort Bruno, Ludovica
collection PubMed
description Here, we report data concerning the discovery in adult human peripheral blood of a precursor cell population able to differentiate into CD4(+)CD3(+)αβ(+) mature T cells. These cells, which represent 0.1–0.5% of total peripheral blood mononuclear cells (PBMC), express substantial levels of CD4, but lack CD3 surface expression. At a molecular level, they express the pre-T cell receptor α (pTα) gene, CD3-γ, CD-δ and CD-ε, and RAG-1 recombination enzyme and have initiated rearrangements in the T cell receptor (TCR)-β locus (D–J). Moreover, low levels of CD3ε protein, but not of TCR-β chain, can be detected in their cytoplasm. Our results suggest that CD4(+)CD3(−) cells identified in peripheral blood are different from CD3(−)CD4(+)CD8(−) thymocytes and may contain precursors of an extrathymic T cell differentiation pathway.
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spelling pubmed-21961712008-04-16 Identification of a Committed T Cell Precursor Population in Adult Human Peripheral Blood Bruno, Ludovica Res, Pieter Dessing, Mark Cella, Marina Spits, Hergen J Exp Med Article Here, we report data concerning the discovery in adult human peripheral blood of a precursor cell population able to differentiate into CD4(+)CD3(+)αβ(+) mature T cells. These cells, which represent 0.1–0.5% of total peripheral blood mononuclear cells (PBMC), express substantial levels of CD4, but lack CD3 surface expression. At a molecular level, they express the pre-T cell receptor α (pTα) gene, CD3-γ, CD-δ and CD-ε, and RAG-1 recombination enzyme and have initiated rearrangements in the T cell receptor (TCR)-β locus (D–J). Moreover, low levels of CD3ε protein, but not of TCR-β chain, can be detected in their cytoplasm. Our results suggest that CD4(+)CD3(−) cells identified in peripheral blood are different from CD3(−)CD4(+)CD8(−) thymocytes and may contain precursors of an extrathymic T cell differentiation pathway. The Rockefeller University Press 1997-03-03 /pmc/articles/PMC2196171/ /pubmed/9120393 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 Article
Bruno, Ludovica
Res, Pieter
Dessing, Mark
Cella, Marina
Spits, Hergen
Identification of a Committed T Cell Precursor Population in Adult Human Peripheral Blood
title Identification of a Committed T Cell Precursor Population in Adult Human Peripheral Blood
title_full Identification of a Committed T Cell Precursor Population in Adult Human Peripheral Blood
title_fullStr Identification of a Committed T Cell Precursor Population in Adult Human Peripheral Blood
title_full_unstemmed Identification of a Committed T Cell Precursor Population in Adult Human Peripheral Blood
title_short Identification of a Committed T Cell Precursor Population in Adult Human Peripheral Blood
title_sort identification of a committed t cell precursor population in adult human peripheral blood
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2196171/
https://www.ncbi.nlm.nih.gov/pubmed/9120393
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