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Major T Cell Progenitor Activity in Bone Marrow–derived Spleen Colonies
Common lymphoid progenitors (CLP) are generated in adult bone marrow (BM), but the intermediate steps leading to T cell commitment are unknown, and so is the site at which this commitment occurs. Here, we show that colonies arising in the spleen 12 days after BM injection harbor T cell precursors th...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2002
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2193723/ https://www.ncbi.nlm.nih.gov/pubmed/11927635 http://dx.doi.org/10.1084/jem.20011475 |
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author | Lancrin, Christophe Schneider, Elke Lambolez, Florence Arcangeli, Marie-Laure Garcia-Cordier, Corinne Rocha, Benedita Ezine, Sophie |
author_facet | Lancrin, Christophe Schneider, Elke Lambolez, Florence Arcangeli, Marie-Laure Garcia-Cordier, Corinne Rocha, Benedita Ezine, Sophie |
author_sort | Lancrin, Christophe |
collection | PubMed |
description | Common lymphoid progenitors (CLP) are generated in adult bone marrow (BM), but the intermediate steps leading to T cell commitment are unknown, and so is the site at which this commitment occurs. Here, we show that colonies arising in the spleen 12 days after BM injection harbor T cell precursors that are undetectable in BM. These precursors did not generate myeloid cells in vivo but repopulated the thymus and the peripheral T cell compartment much faster than did CLP. Two lineage negative (Lin(−)) subpopulations were distinguished, namely CD44(+) Thy1(−) cells still capable of natural killer generation and transient low-level B cell generation, and T cell–restricted CD44(−) Thy1(+) cells. At a molecular level, frequency of CD3ɛ and preTα mRNA was very different in each subset. Furthermore, only the CD44(−) Thy1(+) subset have initiated rearrangements in the T cell receptor β locus. Thus, this study identifies extramedullary T cell progenitors and will allow easy approach to T cell commitment studies. |
format | Text |
id | pubmed-2193723 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2002 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21937232008-04-14 Major T Cell Progenitor Activity in Bone Marrow–derived Spleen Colonies Lancrin, Christophe Schneider, Elke Lambolez, Florence Arcangeli, Marie-Laure Garcia-Cordier, Corinne Rocha, Benedita Ezine, Sophie J Exp Med Original Article Common lymphoid progenitors (CLP) are generated in adult bone marrow (BM), but the intermediate steps leading to T cell commitment are unknown, and so is the site at which this commitment occurs. Here, we show that colonies arising in the spleen 12 days after BM injection harbor T cell precursors that are undetectable in BM. These precursors did not generate myeloid cells in vivo but repopulated the thymus and the peripheral T cell compartment much faster than did CLP. Two lineage negative (Lin(−)) subpopulations were distinguished, namely CD44(+) Thy1(−) cells still capable of natural killer generation and transient low-level B cell generation, and T cell–restricted CD44(−) Thy1(+) cells. At a molecular level, frequency of CD3ɛ and preTα mRNA was very different in each subset. Furthermore, only the CD44(−) Thy1(+) subset have initiated rearrangements in the T cell receptor β locus. Thus, this study identifies extramedullary T cell progenitors and will allow easy approach to T cell commitment studies. The Rockefeller University Press 2002-04-01 /pmc/articles/PMC2193723/ /pubmed/11927635 http://dx.doi.org/10.1084/jem.20011475 Text en Copyright © 2002, The Rockefeller University Press 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 | Original Article Lancrin, Christophe Schneider, Elke Lambolez, Florence Arcangeli, Marie-Laure Garcia-Cordier, Corinne Rocha, Benedita Ezine, Sophie Major T Cell Progenitor Activity in Bone Marrow–derived Spleen Colonies |
title | Major T Cell Progenitor Activity in Bone Marrow–derived Spleen Colonies |
title_full | Major T Cell Progenitor Activity in Bone Marrow–derived Spleen Colonies |
title_fullStr | Major T Cell Progenitor Activity in Bone Marrow–derived Spleen Colonies |
title_full_unstemmed | Major T Cell Progenitor Activity in Bone Marrow–derived Spleen Colonies |
title_short | Major T Cell Progenitor Activity in Bone Marrow–derived Spleen Colonies |
title_sort | major t cell progenitor activity in bone marrow–derived spleen colonies |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2193723/ https://www.ncbi.nlm.nih.gov/pubmed/11927635 http://dx.doi.org/10.1084/jem.20011475 |
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