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Two rare populations of mouse Thy-1lo bone marrow cells repopulate the thymus

Two-color FACS analysis of mouse bone marrow reveals a rare population, comprising 0.1-0.3% of the total, that expresses low levels of the Thy- 1 antigen but does not express any of five surface markers that characterize differentiated hematolymphoid cells. We demonstrate here that this fraction of...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1988
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2188943/
https://www.ncbi.nlm.nih.gov/pubmed/2896758
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description Two-color FACS analysis of mouse bone marrow reveals a rare population, comprising 0.1-0.3% of the total, that expresses low levels of the Thy- 1 antigen but does not express any of five surface markers that characterize differentiated hematolymphoid cells. We demonstrate here that this fraction of mouse bone marrow is enormously enriched in cells that can home to the thymus and differentiate into mature T lymphocytes, subsequently migrating to peripheral lymphoid organs. Only a subset of the FACS-isolated fraction (1/90 after intrathymic injection) is capable of responding to the thymic microenvironment with a productive commitment to the T cell lineage. A second fraction of mouse bone marrow, which expresses how levels of Thy-1 but is also positive for at least one of five hematolymphoid lineage-specific markers, also contains cells that home to the thymus and establish colonies of thymocytes. The two fractions each contribute approximately equal amounts of thymic colony-forming units (CFUt) to the bone marrow, and together can account for at least half of the CFUt in whole bone marrow.
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spelling pubmed-21889432008-04-17 Two rare populations of mouse Thy-1lo bone marrow cells repopulate the thymus J Exp Med Articles Two-color FACS analysis of mouse bone marrow reveals a rare population, comprising 0.1-0.3% of the total, that expresses low levels of the Thy- 1 antigen but does not express any of five surface markers that characterize differentiated hematolymphoid cells. We demonstrate here that this fraction of mouse bone marrow is enormously enriched in cells that can home to the thymus and differentiate into mature T lymphocytes, subsequently migrating to peripheral lymphoid organs. Only a subset of the FACS-isolated fraction (1/90 after intrathymic injection) is capable of responding to the thymic microenvironment with a productive commitment to the T cell lineage. A second fraction of mouse bone marrow, which expresses how levels of Thy-1 but is also positive for at least one of five hematolymphoid lineage-specific markers, also contains cells that home to the thymus and establish colonies of thymocytes. The two fractions each contribute approximately equal amounts of thymic colony-forming units (CFUt) to the bone marrow, and together can account for at least half of the CFUt in whole bone marrow. The Rockefeller University Press 1988-05-01 /pmc/articles/PMC2188943/ /pubmed/2896758 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
Two rare populations of mouse Thy-1lo bone marrow cells repopulate the thymus
title Two rare populations of mouse Thy-1lo bone marrow cells repopulate the thymus
title_full Two rare populations of mouse Thy-1lo bone marrow cells repopulate the thymus
title_fullStr Two rare populations of mouse Thy-1lo bone marrow cells repopulate the thymus
title_full_unstemmed Two rare populations of mouse Thy-1lo bone marrow cells repopulate the thymus
title_short Two rare populations of mouse Thy-1lo bone marrow cells repopulate the thymus
title_sort two rare populations of mouse thy-1lo bone marrow cells repopulate the thymus
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2188943/
https://www.ncbi.nlm.nih.gov/pubmed/2896758