Progressive Changes in CXCR4 Expression That Define Thymocyte Positive Selection Are Dispensable For Both Innate and Conventional αβT-cell Development

Abstract The ordered migration of immature thymocytes through thymic microenvironments generates both adaptive MHC restricted αβT-cells and innate CD1d-restricted iNKT-cells. While several chemokine receptors and ligands control multiple stages of this process, their involvement during early thymocy...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Beth Lucas, Andrea J. White, Sonia M. Parnell, Peter M. Henley, William E. Jenkinson, Graham Anderson
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2017
Materias:
R
Q
Acceso en línea:https://doaj.org/article/b9b26475765442e6a982e5ae43e28e35
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:b9b26475765442e6a982e5ae43e28e35
record_format dspace
spelling oai:doaj.org-article:b9b26475765442e6a982e5ae43e28e352021-12-02T15:05:24ZProgressive Changes in CXCR4 Expression That Define Thymocyte Positive Selection Are Dispensable For Both Innate and Conventional αβT-cell Development10.1038/s41598-017-05182-72045-2322https://doaj.org/article/b9b26475765442e6a982e5ae43e28e352017-07-01T00:00:00Zhttps://doi.org/10.1038/s41598-017-05182-7https://doaj.org/toc/2045-2322Abstract The ordered migration of immature thymocytes through thymic microenvironments generates both adaptive MHC restricted αβT-cells and innate CD1d-restricted iNKT-cells. While several chemokine receptors and ligands control multiple stages of this process, their involvement during early thymocyte development often precludes direct analysis of potential roles during later developmental stages. For example, because of early lethality of CXCR4−/− mice, and stage-specific requirements for CXCR4 in thymus colonisation and pre-TCR mediated selection, its role in thymic positive selection is unclear. Here we have examined CXCR4-CXCL12 interactions during the maturation of CD4+CD8+ thymocytes, including downstream stages of iNKT and αβT-cell development. We show CXCL12 expression is a common feature of cortical thymic epithelial cells, indicating widespread availability throughout the cortex. Moreover, CXCR4 expression by CD4+CD8+ pre-selection thymocytes is progressively downregulated following both MHC and CD1d-restricted thymic selection events. However, using CD4Cre-mediated deletion to bypass its involvement in CD4−CD8− thymocyte development, we show CXCR4 is dispensable for the maintenance and intrathymic positioning of CD4+CD8+ thymocytes, and their ability to generate mature αβT-cells and CD1d-restricted iNKT-cells. Collectively, our data define dynamic changes in CXCR4 expression as a marker for intrathymic selection events, and show its role in T-cell development is restricted to pre-CD4+CD8+ stages.Beth LucasAndrea J. WhiteSonia M. ParnellPeter M. HenleyWilliam E. JenkinsonGraham AndersonNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 7, Iss 1, Pp 1-11 (2017)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Beth Lucas
Andrea J. White
Sonia M. Parnell
Peter M. Henley
William E. Jenkinson
Graham Anderson
Progressive Changes in CXCR4 Expression That Define Thymocyte Positive Selection Are Dispensable For Both Innate and Conventional αβT-cell Development
description Abstract The ordered migration of immature thymocytes through thymic microenvironments generates both adaptive MHC restricted αβT-cells and innate CD1d-restricted iNKT-cells. While several chemokine receptors and ligands control multiple stages of this process, their involvement during early thymocyte development often precludes direct analysis of potential roles during later developmental stages. For example, because of early lethality of CXCR4−/− mice, and stage-specific requirements for CXCR4 in thymus colonisation and pre-TCR mediated selection, its role in thymic positive selection is unclear. Here we have examined CXCR4-CXCL12 interactions during the maturation of CD4+CD8+ thymocytes, including downstream stages of iNKT and αβT-cell development. We show CXCL12 expression is a common feature of cortical thymic epithelial cells, indicating widespread availability throughout the cortex. Moreover, CXCR4 expression by CD4+CD8+ pre-selection thymocytes is progressively downregulated following both MHC and CD1d-restricted thymic selection events. However, using CD4Cre-mediated deletion to bypass its involvement in CD4−CD8− thymocyte development, we show CXCR4 is dispensable for the maintenance and intrathymic positioning of CD4+CD8+ thymocytes, and their ability to generate mature αβT-cells and CD1d-restricted iNKT-cells. Collectively, our data define dynamic changes in CXCR4 expression as a marker for intrathymic selection events, and show its role in T-cell development is restricted to pre-CD4+CD8+ stages.
format article
author Beth Lucas
Andrea J. White
Sonia M. Parnell
Peter M. Henley
William E. Jenkinson
Graham Anderson
author_facet Beth Lucas
Andrea J. White
Sonia M. Parnell
Peter M. Henley
William E. Jenkinson
Graham Anderson
author_sort Beth Lucas
title Progressive Changes in CXCR4 Expression That Define Thymocyte Positive Selection Are Dispensable For Both Innate and Conventional αβT-cell Development
title_short Progressive Changes in CXCR4 Expression That Define Thymocyte Positive Selection Are Dispensable For Both Innate and Conventional αβT-cell Development
title_full Progressive Changes in CXCR4 Expression That Define Thymocyte Positive Selection Are Dispensable For Both Innate and Conventional αβT-cell Development
title_fullStr Progressive Changes in CXCR4 Expression That Define Thymocyte Positive Selection Are Dispensable For Both Innate and Conventional αβT-cell Development
title_full_unstemmed Progressive Changes in CXCR4 Expression That Define Thymocyte Positive Selection Are Dispensable For Both Innate and Conventional αβT-cell Development
title_sort progressive changes in cxcr4 expression that define thymocyte positive selection are dispensable for both innate and conventional αβt-cell development
publisher Nature Portfolio
publishDate 2017
url https://doaj.org/article/b9b26475765442e6a982e5ae43e28e35
work_keys_str_mv AT bethlucas progressivechangesincxcr4expressionthatdefinethymocytepositiveselectionaredispensableforbothinnateandconventionalabtcelldevelopment
AT andreajwhite progressivechangesincxcr4expressionthatdefinethymocytepositiveselectionaredispensableforbothinnateandconventionalabtcelldevelopment
AT soniamparnell progressivechangesincxcr4expressionthatdefinethymocytepositiveselectionaredispensableforbothinnateandconventionalabtcelldevelopment
AT petermhenley progressivechangesincxcr4expressionthatdefinethymocytepositiveselectionaredispensableforbothinnateandconventionalabtcelldevelopment
AT williamejenkinson progressivechangesincxcr4expressionthatdefinethymocytepositiveselectionaredispensableforbothinnateandconventionalabtcelldevelopment
AT grahamanderson progressivechangesincxcr4expressionthatdefinethymocytepositiveselectionaredispensableforbothinnateandconventionalabtcelldevelopment
_version_ 1718388854370598912