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Maturation-Dependent Licensing of Naive T Cells for Rapid TNF Production

The peripheral naïve T cell pool is comprised of a heterogeneous population of cells at various stages of development, which is a process that begins in the thymus and is completed after a post-thymic maturation phase in the periphery. One hallmark of naïve T cells in secondary lymphoid organs is th...

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Autores principales: Priyadharshini, Bhavana, Welsh, Raymond M., Greiner, Dale L., Gerstein, Rachel M., Brehm, Michael A.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2991336/
https://www.ncbi.nlm.nih.gov/pubmed/21124839
http://dx.doi.org/10.1371/journal.pone.0015038
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author Priyadharshini, Bhavana
Welsh, Raymond M.
Greiner, Dale L.
Gerstein, Rachel M.
Brehm, Michael A.
author_facet Priyadharshini, Bhavana
Welsh, Raymond M.
Greiner, Dale L.
Gerstein, Rachel M.
Brehm, Michael A.
author_sort Priyadharshini, Bhavana
collection PubMed
description The peripheral naïve T cell pool is comprised of a heterogeneous population of cells at various stages of development, which is a process that begins in the thymus and is completed after a post-thymic maturation phase in the periphery. One hallmark of naïve T cells in secondary lymphoid organs is their unique ability to produce TNF rapidly after activation and prior to acquiring other effector functions. To determine how maturation influences the licensing of naïve T cells to produce TNF, we compared cytokine profiles of CD4(+) and CD8(+) single positive (SP) thymocytes, recent thymic emigrants (RTEs) and mature-naïve (MN) T cells during TCR activation. SP thymocytes exhibited a poor ability to produce TNF when compared to splenic T cells despite expressing similar TCR levels and possessing comparable activation kinetics (upregulation of CD25 and CD69). Provision of optimal antigen presenting cells from the spleen did not fully enable SP thymocytes to produce TNF, suggesting an intrinsic defect in their ability to produce TNF efficiently. Using a thymocyte adoptive transfer model, we demonstrate that the ability of T cells to produce TNF increases progressively with time in the periphery as a function of their maturation state. RTEs that were identified in NG-BAC transgenic mice by the expression of GFP showed a significantly enhanced ability to express TNF relative to SP thymocytes but not to the extent of fully MN T cells. Together, these findings suggest that TNF expression by naïve T cells is regulated via a gradual licensing process that requires functional maturation in peripheral lymphoid organs.
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spelling pubmed-29913362010-12-01 Maturation-Dependent Licensing of Naive T Cells for Rapid TNF Production Priyadharshini, Bhavana Welsh, Raymond M. Greiner, Dale L. Gerstein, Rachel M. Brehm, Michael A. PLoS One Research Article The peripheral naïve T cell pool is comprised of a heterogeneous population of cells at various stages of development, which is a process that begins in the thymus and is completed after a post-thymic maturation phase in the periphery. One hallmark of naïve T cells in secondary lymphoid organs is their unique ability to produce TNF rapidly after activation and prior to acquiring other effector functions. To determine how maturation influences the licensing of naïve T cells to produce TNF, we compared cytokine profiles of CD4(+) and CD8(+) single positive (SP) thymocytes, recent thymic emigrants (RTEs) and mature-naïve (MN) T cells during TCR activation. SP thymocytes exhibited a poor ability to produce TNF when compared to splenic T cells despite expressing similar TCR levels and possessing comparable activation kinetics (upregulation of CD25 and CD69). Provision of optimal antigen presenting cells from the spleen did not fully enable SP thymocytes to produce TNF, suggesting an intrinsic defect in their ability to produce TNF efficiently. Using a thymocyte adoptive transfer model, we demonstrate that the ability of T cells to produce TNF increases progressively with time in the periphery as a function of their maturation state. RTEs that were identified in NG-BAC transgenic mice by the expression of GFP showed a significantly enhanced ability to express TNF relative to SP thymocytes but not to the extent of fully MN T cells. Together, these findings suggest that TNF expression by naïve T cells is regulated via a gradual licensing process that requires functional maturation in peripheral lymphoid organs. Public Library of Science 2010-11-24 /pmc/articles/PMC2991336/ /pubmed/21124839 http://dx.doi.org/10.1371/journal.pone.0015038 Text en Priyadharshini et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Priyadharshini, Bhavana
Welsh, Raymond M.
Greiner, Dale L.
Gerstein, Rachel M.
Brehm, Michael A.
Maturation-Dependent Licensing of Naive T Cells for Rapid TNF Production
title Maturation-Dependent Licensing of Naive T Cells for Rapid TNF Production
title_full Maturation-Dependent Licensing of Naive T Cells for Rapid TNF Production
title_fullStr Maturation-Dependent Licensing of Naive T Cells for Rapid TNF Production
title_full_unstemmed Maturation-Dependent Licensing of Naive T Cells for Rapid TNF Production
title_short Maturation-Dependent Licensing of Naive T Cells for Rapid TNF Production
title_sort maturation-dependent licensing of naive t cells for rapid tnf production
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2991336/
https://www.ncbi.nlm.nih.gov/pubmed/21124839
http://dx.doi.org/10.1371/journal.pone.0015038
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