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Fas-Mediated Apoptosis Regulates the Composition of Peripheral αβ T Cell Repertoire by Constitutively Purging Out Double Negative T Cells

BACKGROUND: The Fas pathway is a major regulator of T cell homeostasis, however, the T cell population that is controlled by the Fas pathway in vivo is poorly defined. Although CD4 and CD8 single positive (SP) T cells are the two major T cell subsets in the periphery of wild type mice, the repertoir...

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Autores principales: Mohamood, Abdiaziz S., Bargatze, Dylan, Xiao, Zuoxiang, Jie, Chunfa, Yagita, Hideo, Ruben, Dawn, Watson, Julie, Chakravarti, Shukti, Schneck, Jonathan P., Hamad, Abdel Rahim A.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2565807/
https://www.ncbi.nlm.nih.gov/pubmed/18941614
http://dx.doi.org/10.1371/journal.pone.0003465
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author Mohamood, Abdiaziz S.
Bargatze, Dylan
Xiao, Zuoxiang
Jie, Chunfa
Yagita, Hideo
Ruben, Dawn
Watson, Julie
Chakravarti, Shukti
Schneck, Jonathan P.
Hamad, Abdel Rahim A.
author_facet Mohamood, Abdiaziz S.
Bargatze, Dylan
Xiao, Zuoxiang
Jie, Chunfa
Yagita, Hideo
Ruben, Dawn
Watson, Julie
Chakravarti, Shukti
Schneck, Jonathan P.
Hamad, Abdel Rahim A.
author_sort Mohamood, Abdiaziz S.
collection PubMed
description BACKGROUND: The Fas pathway is a major regulator of T cell homeostasis, however, the T cell population that is controlled by the Fas pathway in vivo is poorly defined. Although CD4 and CD8 single positive (SP) T cells are the two major T cell subsets in the periphery of wild type mice, the repertoire of mice bearing loss-of-function mutation in either Fas (lpr mice) or Fas ligand (gld mice) is predominated by CD4(−)CD8(−) double negative αβ T cells that also express B220 and generally referred to as B220(+)DN T cells. Despite extensive analysis, the basis of B220(+)DN T cell lymphoproliferation remains poorly understood. In this study we re-examined the issue of why T cell lymphoproliferation caused by gld mutation is predominated by B220(+)DN T cells. METHODOLOGY AND PRINCIPAL FINDINGS: We combined the following approaches to study this question: Gene transcript profiling, BrdU labeling, and apoptosis assays. Our results show that B220(+)DN T cells are proliferating and dying at exceptionally high rates than SP T cells in the steady state. The high proliferation rate is restricted to B220+DN T cells found in the gut epithelium whereas the high apoptosis rate occurred both in the gut epithelium and periphery. However, only in the periphery, apoptosis of B220(+)DN T cell is Fas-dependent. When the Fas pathway is genetically impaired, apoptosis of peripheral B220(+)DN T cells was reduced to a baseline level similar to that of SP T cells. Under these conditions of normalized apoptosis, B220(+)DN T cells progressively accumulate in the periphery, eventually resulting in B220(+)DN T cell lymphoproliferation. CONCLUSIONS/SIGNIFICANCE: The Fas pathway plays a critical role in regulating the tissue distribution of DN T cells through targeting and elimination of DN T cells from the periphery in the steady state. The results provide new insight into pathogenesis of DN T cell lymphoproliferation.
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spelling pubmed-25658072008-10-21 Fas-Mediated Apoptosis Regulates the Composition of Peripheral αβ T Cell Repertoire by Constitutively Purging Out Double Negative T Cells Mohamood, Abdiaziz S. Bargatze, Dylan Xiao, Zuoxiang Jie, Chunfa Yagita, Hideo Ruben, Dawn Watson, Julie Chakravarti, Shukti Schneck, Jonathan P. Hamad, Abdel Rahim A. PLoS One Research Article BACKGROUND: The Fas pathway is a major regulator of T cell homeostasis, however, the T cell population that is controlled by the Fas pathway in vivo is poorly defined. Although CD4 and CD8 single positive (SP) T cells are the two major T cell subsets in the periphery of wild type mice, the repertoire of mice bearing loss-of-function mutation in either Fas (lpr mice) or Fas ligand (gld mice) is predominated by CD4(−)CD8(−) double negative αβ T cells that also express B220 and generally referred to as B220(+)DN T cells. Despite extensive analysis, the basis of B220(+)DN T cell lymphoproliferation remains poorly understood. In this study we re-examined the issue of why T cell lymphoproliferation caused by gld mutation is predominated by B220(+)DN T cells. METHODOLOGY AND PRINCIPAL FINDINGS: We combined the following approaches to study this question: Gene transcript profiling, BrdU labeling, and apoptosis assays. Our results show that B220(+)DN T cells are proliferating and dying at exceptionally high rates than SP T cells in the steady state. The high proliferation rate is restricted to B220+DN T cells found in the gut epithelium whereas the high apoptosis rate occurred both in the gut epithelium and periphery. However, only in the periphery, apoptosis of B220(+)DN T cell is Fas-dependent. When the Fas pathway is genetically impaired, apoptosis of peripheral B220(+)DN T cells was reduced to a baseline level similar to that of SP T cells. Under these conditions of normalized apoptosis, B220(+)DN T cells progressively accumulate in the periphery, eventually resulting in B220(+)DN T cell lymphoproliferation. CONCLUSIONS/SIGNIFICANCE: The Fas pathway plays a critical role in regulating the tissue distribution of DN T cells through targeting and elimination of DN T cells from the periphery in the steady state. The results provide new insight into pathogenesis of DN T cell lymphoproliferation. Public Library of Science 2008-10-21 /pmc/articles/PMC2565807/ /pubmed/18941614 http://dx.doi.org/10.1371/journal.pone.0003465 Text en Mohamood 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
Mohamood, Abdiaziz S.
Bargatze, Dylan
Xiao, Zuoxiang
Jie, Chunfa
Yagita, Hideo
Ruben, Dawn
Watson, Julie
Chakravarti, Shukti
Schneck, Jonathan P.
Hamad, Abdel Rahim A.
Fas-Mediated Apoptosis Regulates the Composition of Peripheral αβ T Cell Repertoire by Constitutively Purging Out Double Negative T Cells
title Fas-Mediated Apoptosis Regulates the Composition of Peripheral αβ T Cell Repertoire by Constitutively Purging Out Double Negative T Cells
title_full Fas-Mediated Apoptosis Regulates the Composition of Peripheral αβ T Cell Repertoire by Constitutively Purging Out Double Negative T Cells
title_fullStr Fas-Mediated Apoptosis Regulates the Composition of Peripheral αβ T Cell Repertoire by Constitutively Purging Out Double Negative T Cells
title_full_unstemmed Fas-Mediated Apoptosis Regulates the Composition of Peripheral αβ T Cell Repertoire by Constitutively Purging Out Double Negative T Cells
title_short Fas-Mediated Apoptosis Regulates the Composition of Peripheral αβ T Cell Repertoire by Constitutively Purging Out Double Negative T Cells
title_sort fas-mediated apoptosis regulates the composition of peripheral αβ t cell repertoire by constitutively purging out double negative t cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2565807/
https://www.ncbi.nlm.nih.gov/pubmed/18941614
http://dx.doi.org/10.1371/journal.pone.0003465
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