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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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Detalles Bibliográficos
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
Descripción
Sumario: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.