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Extrathymic T Cell Lymphopoiesis: Ontogeny and Contribution to Gut Intraepithelial Lymphocytes in Athymic and Euthymic Mice

In the absence of thymopoiesis, T lymphocytes are nevertheless present, mainly in the gut epithelium. Ontogeny of the extrathymic pathway and the extent of its involvement in euthymic mice are controversial. These questions have been addressed by assessing the expression of recombinase activating ge...

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Autores principales: Guy-Grand, Delphine, Azogui, Orly, Celli, Susanna, Darche, Sylvie, Nussenzweig, Michel C., Kourilsky, Philippe, Vassalli, Pierre
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2003
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2193840/
https://www.ncbi.nlm.nih.gov/pubmed/12566417
http://dx.doi.org/10.1084/jem.20021639
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author Guy-Grand, Delphine
Azogui, Orly
Celli, Susanna
Darche, Sylvie
Nussenzweig, Michel C.
Kourilsky, Philippe
Vassalli, Pierre
author_facet Guy-Grand, Delphine
Azogui, Orly
Celli, Susanna
Darche, Sylvie
Nussenzweig, Michel C.
Kourilsky, Philippe
Vassalli, Pierre
author_sort Guy-Grand, Delphine
collection PubMed
description In the absence of thymopoiesis, T lymphocytes are nevertheless present, mainly in the gut epithelium. Ontogeny of the extrathymic pathway and the extent of its involvement in euthymic mice are controversial. These questions have been addressed by assessing the expression of recombinase activating gene (RAG) through the use of green fluorescent protein RAG2 transgenic mouse models. In athymic mice, T lymphopoiesis occurs mainly in the mesenteric lymph node and less in the Peyer's patches. Ontogenic steps of this lymphopoiesis resemble those of thymopoiesis, but with an apparent bias toward γδ T cell production and with a paucity of oligoclonal αβ T cells possibly resulting from a deficit in positive selection. Whether in athymic or euthymic mice, neither T intraepithelial lymphocytes (IEL) nor cryptopatch cells (reported to contain precursors of IEL) displayed fluorescence indicating recent RAG protein synthesis. Newly made T cells migrate from the mesenteric node into the thoracic duct lymph to reach the gut mucosa. In euthymic mice, this extrathymic pathway is totally repressed, except in conditions of severe lymphocytic depletion. Thus, in normal animals, all gut T IEL, including CD8αα(+) cells, are of thymic origin, CD8αα(+) TCRαβ(+) IEL being the likely progeny of double negative NK1-1(−) thymocytes, which show polyclonal Vα and Vβ repertoires.
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spelling pubmed-21938402008-04-11 Extrathymic T Cell Lymphopoiesis: Ontogeny and Contribution to Gut Intraepithelial Lymphocytes in Athymic and Euthymic Mice Guy-Grand, Delphine Azogui, Orly Celli, Susanna Darche, Sylvie Nussenzweig, Michel C. Kourilsky, Philippe Vassalli, Pierre J Exp Med Article In the absence of thymopoiesis, T lymphocytes are nevertheless present, mainly in the gut epithelium. Ontogeny of the extrathymic pathway and the extent of its involvement in euthymic mice are controversial. These questions have been addressed by assessing the expression of recombinase activating gene (RAG) through the use of green fluorescent protein RAG2 transgenic mouse models. In athymic mice, T lymphopoiesis occurs mainly in the mesenteric lymph node and less in the Peyer's patches. Ontogenic steps of this lymphopoiesis resemble those of thymopoiesis, but with an apparent bias toward γδ T cell production and with a paucity of oligoclonal αβ T cells possibly resulting from a deficit in positive selection. Whether in athymic or euthymic mice, neither T intraepithelial lymphocytes (IEL) nor cryptopatch cells (reported to contain precursors of IEL) displayed fluorescence indicating recent RAG protein synthesis. Newly made T cells migrate from the mesenteric node into the thoracic duct lymph to reach the gut mucosa. In euthymic mice, this extrathymic pathway is totally repressed, except in conditions of severe lymphocytic depletion. Thus, in normal animals, all gut T IEL, including CD8αα(+) cells, are of thymic origin, CD8αα(+) TCRαβ(+) IEL being the likely progeny of double negative NK1-1(−) thymocytes, which show polyclonal Vα and Vβ repertoires. The Rockefeller University Press 2003-02-03 /pmc/articles/PMC2193840/ /pubmed/12566417 http://dx.doi.org/10.1084/jem.20021639 Text en Copyright © 2003, 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 Article
Guy-Grand, Delphine
Azogui, Orly
Celli, Susanna
Darche, Sylvie
Nussenzweig, Michel C.
Kourilsky, Philippe
Vassalli, Pierre
Extrathymic T Cell Lymphopoiesis: Ontogeny and Contribution to Gut Intraepithelial Lymphocytes in Athymic and Euthymic Mice
title Extrathymic T Cell Lymphopoiesis: Ontogeny and Contribution to Gut Intraepithelial Lymphocytes in Athymic and Euthymic Mice
title_full Extrathymic T Cell Lymphopoiesis: Ontogeny and Contribution to Gut Intraepithelial Lymphocytes in Athymic and Euthymic Mice
title_fullStr Extrathymic T Cell Lymphopoiesis: Ontogeny and Contribution to Gut Intraepithelial Lymphocytes in Athymic and Euthymic Mice
title_full_unstemmed Extrathymic T Cell Lymphopoiesis: Ontogeny and Contribution to Gut Intraepithelial Lymphocytes in Athymic and Euthymic Mice
title_short Extrathymic T Cell Lymphopoiesis: Ontogeny and Contribution to Gut Intraepithelial Lymphocytes in Athymic and Euthymic Mice
title_sort extrathymic t cell lymphopoiesis: ontogeny and contribution to gut intraepithelial lymphocytes in athymic and euthymic mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2193840/
https://www.ncbi.nlm.nih.gov/pubmed/12566417
http://dx.doi.org/10.1084/jem.20021639
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