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Developmental regulation of Foxp3 expression during ontogeny

Thymectomy of neonatal mice can result in the development of autoimmune pathology. It has been proposed that thymic output of regulatory T (T reg) cells is delayed during ontogeny and that the development of autoimmune disease in neonatally thymectomized mice is caused by the escape of self-reactive...

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Autores principales: Fontenot, Jason D., Dooley, James L., Farr, Andrew G., Rudensky, Alexander Y.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2213175/
https://www.ncbi.nlm.nih.gov/pubmed/16203863
http://dx.doi.org/10.1084/jem.20050784
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author Fontenot, Jason D.
Dooley, James L.
Farr, Andrew G.
Rudensky, Alexander Y.
author_facet Fontenot, Jason D.
Dooley, James L.
Farr, Andrew G.
Rudensky, Alexander Y.
author_sort Fontenot, Jason D.
collection PubMed
description Thymectomy of neonatal mice can result in the development of autoimmune pathology. It has been proposed that thymic output of regulatory T (T reg) cells is delayed during ontogeny and that the development of autoimmune disease in neonatally thymectomized mice is caused by the escape of self-reactive T cells before thymectomy without accompanying T reg cells. However, the kinetics of T reg cell production within the thymus during ontogeny has not been assessed. We demonstrate that the development of Foxp3-expressing T reg cells is substantially delayed relative to nonregulatory thymocytes during ontogeny. Based on our data, we speculate that induction of Foxp3 in developing thymocytes and, thus, commitment to the T reg cell lineage is facilitated by a signal largely associated with the thymic medulla.
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spelling pubmed-22131752008-03-11 Developmental regulation of Foxp3 expression during ontogeny Fontenot, Jason D. Dooley, James L. Farr, Andrew G. Rudensky, Alexander Y. J Exp Med Brief Definitive Report Thymectomy of neonatal mice can result in the development of autoimmune pathology. It has been proposed that thymic output of regulatory T (T reg) cells is delayed during ontogeny and that the development of autoimmune disease in neonatally thymectomized mice is caused by the escape of self-reactive T cells before thymectomy without accompanying T reg cells. However, the kinetics of T reg cell production within the thymus during ontogeny has not been assessed. We demonstrate that the development of Foxp3-expressing T reg cells is substantially delayed relative to nonregulatory thymocytes during ontogeny. Based on our data, we speculate that induction of Foxp3 in developing thymocytes and, thus, commitment to the T reg cell lineage is facilitated by a signal largely associated with the thymic medulla. The Rockefeller University Press 2005-10-03 /pmc/articles/PMC2213175/ /pubmed/16203863 http://dx.doi.org/10.1084/jem.20050784 Text en Copyright © 2005, 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 Brief Definitive Report
Fontenot, Jason D.
Dooley, James L.
Farr, Andrew G.
Rudensky, Alexander Y.
Developmental regulation of Foxp3 expression during ontogeny
title Developmental regulation of Foxp3 expression during ontogeny
title_full Developmental regulation of Foxp3 expression during ontogeny
title_fullStr Developmental regulation of Foxp3 expression during ontogeny
title_full_unstemmed Developmental regulation of Foxp3 expression during ontogeny
title_short Developmental regulation of Foxp3 expression during ontogeny
title_sort developmental regulation of foxp3 expression during ontogeny
topic Brief Definitive Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2213175/
https://www.ncbi.nlm.nih.gov/pubmed/16203863
http://dx.doi.org/10.1084/jem.20050784
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