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The Importation of Hematogenous Precursors by the Thymus Is a Gated Phenomenon in Normal Adult Mice

Hematogenous precursors repopulate the thymus of normal adult mice, but it is not known whether this process is continuous or intermittent. Here, two approaches were used to demonstrate that the importation of prothymocytes in adult life is a gated phenomenon. In the first, age-dependent receptivity...

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Autores principales: Foss, Deborah L., Donskoy, Elina, Goldschneider, Irving
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2001
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2195915/
https://www.ncbi.nlm.nih.gov/pubmed/11157056
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author Foss, Deborah L.
Donskoy, Elina
Goldschneider, Irving
author_facet Foss, Deborah L.
Donskoy, Elina
Goldschneider, Irving
author_sort Foss, Deborah L.
collection PubMed
description Hematogenous precursors repopulate the thymus of normal adult mice, but it is not known whether this process is continuous or intermittent. Here, two approaches were used to demonstrate that the importation of prothymocytes in adult life is a gated phenomenon. In the first, age-dependent receptivity to thymic chimerism was studied in nonirradiated Ly 5 congenic mice by quantitative intrathymic and intravenous bone marrow (BM) adoptive transfer assays. In the second, the kinetics of importation of blood-borne prothymocytes was determined by timed separation of parabiotic mice. The results showed that >60% of 3–18-wk-old mice developed thymic chimerism after intrathymic injection of BM cells, and that the levels of chimerism (range, 5–90% donor-origin cells) varied cyclically (periodicity, 3 to 5 wk). In contrast, only 11–14% of intravenously injected recipients became chimeric, and chimerism occurred intermittently (receptive period ∼1 wk; refractory period ∼3 wk). In the intravenously injected mice, chimerism occurred simultaneously in both thymic lobes; gate opening occurred only after most intrathymic niches for prothymocytes had emptied; and the ensuing wave of thymocytopoiesis encompassed two periods of gating. These kinetics were confirmed in parabiotic mice, and in cohorts of mice in whom gating was synchronized by an initial intrathymic injection of BM cells. In addition, a protocol was developed by which sequential intravenous injections of BM cells over a 3 to 4 wk period routinely induces thymic chimerism in the apparent absence of stem cell chimerism. Hence, the results not only provide a new paradigm for the regulation of prothymocyte importation during adult life, but may also have applied implications for the selective induction of thymocytopoiesis in nonmyeloablated hosts.
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spelling pubmed-21959152008-04-14 The Importation of Hematogenous Precursors by the Thymus Is a Gated Phenomenon in Normal Adult Mice Foss, Deborah L. Donskoy, Elina Goldschneider, Irving J Exp Med Original Article Hematogenous precursors repopulate the thymus of normal adult mice, but it is not known whether this process is continuous or intermittent. Here, two approaches were used to demonstrate that the importation of prothymocytes in adult life is a gated phenomenon. In the first, age-dependent receptivity to thymic chimerism was studied in nonirradiated Ly 5 congenic mice by quantitative intrathymic and intravenous bone marrow (BM) adoptive transfer assays. In the second, the kinetics of importation of blood-borne prothymocytes was determined by timed separation of parabiotic mice. The results showed that >60% of 3–18-wk-old mice developed thymic chimerism after intrathymic injection of BM cells, and that the levels of chimerism (range, 5–90% donor-origin cells) varied cyclically (periodicity, 3 to 5 wk). In contrast, only 11–14% of intravenously injected recipients became chimeric, and chimerism occurred intermittently (receptive period ∼1 wk; refractory period ∼3 wk). In the intravenously injected mice, chimerism occurred simultaneously in both thymic lobes; gate opening occurred only after most intrathymic niches for prothymocytes had emptied; and the ensuing wave of thymocytopoiesis encompassed two periods of gating. These kinetics were confirmed in parabiotic mice, and in cohorts of mice in whom gating was synchronized by an initial intrathymic injection of BM cells. In addition, a protocol was developed by which sequential intravenous injections of BM cells over a 3 to 4 wk period routinely induces thymic chimerism in the apparent absence of stem cell chimerism. Hence, the results not only provide a new paradigm for the regulation of prothymocyte importation during adult life, but may also have applied implications for the selective induction of thymocytopoiesis in nonmyeloablated hosts. The Rockefeller University Press 2001-02-05 /pmc/articles/PMC2195915/ /pubmed/11157056 Text en © 2001 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
Foss, Deborah L.
Donskoy, Elina
Goldschneider, Irving
The Importation of Hematogenous Precursors by the Thymus Is a Gated Phenomenon in Normal Adult Mice
title The Importation of Hematogenous Precursors by the Thymus Is a Gated Phenomenon in Normal Adult Mice
title_full The Importation of Hematogenous Precursors by the Thymus Is a Gated Phenomenon in Normal Adult Mice
title_fullStr The Importation of Hematogenous Precursors by the Thymus Is a Gated Phenomenon in Normal Adult Mice
title_full_unstemmed The Importation of Hematogenous Precursors by the Thymus Is a Gated Phenomenon in Normal Adult Mice
title_short The Importation of Hematogenous Precursors by the Thymus Is a Gated Phenomenon in Normal Adult Mice
title_sort importation of hematogenous precursors by the thymus is a gated phenomenon in normal adult mice
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2195915/
https://www.ncbi.nlm.nih.gov/pubmed/11157056
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