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IL-2 prevents deletion of developing T-regulatory cells in the thymus.
Hu, Daniel Y; Wirasinha, Rushika C; Goodnow, Christopher C; Daley, Stephen R.
Afiliação
  • Hu DY; Immunology Department, The John Curtin School of Medical Research, The Australian National University, Canberra 0200, Australia.
  • Wirasinha RC; Infection and Immunity Program, Monash Biomedicine Discovery Institute and Department of Biochemistry and Molecular Biology, Monash University, Melbourne, VIC 3800, Australia.
  • Goodnow CC; Immunology Department, The John Curtin School of Medical Research, The Australian National University, Canberra 0200, Australia.
  • Daley SR; Immunology Division, Garvan Institute of Medical Research, Sydney, NSW 2010, Australia.
Cell Death Differ ; 24(6): 1007-1016, 2017 06.
Article em En | MEDLINE | ID: mdl-28362433
ABSTRACT
In the thymus, strongly self-reactive T cells may undergo apoptotic deletion or differentiate into Foxp3+ T-regulatory (T-reg) cells. Mechanisms that partition T cells into these two fates are unclear. Here, we show that IL-2 signalling is required to prevent deletion of CD4+ CD8- CCR7+ Helios+ thymocytes poised to upregulate Foxp3. The deletion prevented by IL-2 signalling is Foxp3 independent and occurs later in thymocyte development than the deletion that is prevented by Card11 signalling. Our results distinguish two bottlenecks at which strongly self-reactive thymocytes undergo deletion or progress to the next stage of T-reg differentiation; Card11 regulates the first bottleneck and IL-2 regulates the second.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Timo / Transdução de Sinais / Interleucina-2 / Linfócitos T Reguladores Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Timo / Transdução de Sinais / Interleucina-2 / Linfócitos T Reguladores Idioma: En Ano de publicação: 2017 Tipo de documento: Article