An essential role for the IL-2 receptor in T cell function.

TitleAn essential role for the IL-2 receptor in T cell function.
Publication TypeJournal Article
Year of Publication2016
AuthorsChinen T, Kannan AK, Levine AG, Fan X, Klein U, Zheng Y, Gasteiger G, Feng Y, Fontenot JD, Rudensky AY
JournalNat Immunol
Volume17
Issue11
Pagination1322-1333
Date Published2016 Nov
ISSN1529-2916
KeywordsAnimals, Biomarkers, CD8-Positive T-Lymphocytes, Cytokines, Female, Immunomodulation, Male, Mice, Mice, Knockout, Mice, Transgenic, Phenotype, Receptors, Interleukin-2, STAT5 Transcription Factor, T-Lymphocyte Subsets, T-Lymphocytes, Regulatory
Abstract

Regulatory T cells (T cells), which have abundant expression of the interleukin 2 receptor (IL-2R), are reliant on IL-2 produced by activated T cells. This feature indicates a key role for a simple network based on the consumption of IL-2 by T cells in their suppressor function. However, congenital deficiency in IL-2R results in reduced expression of the T cell lineage-specification factor Foxp3, which has confounded experimental efforts to understand the role of IL-2R expression and signaling in the suppressor function of T cells. Using genetic gain- and loss-of-function approaches, we found that capture of IL-2 was dispensable for the control of CD4 T cells but was important for limiting the activation of CD8 T cells, and that IL-2R-dependent activation of the transcription factor STAT5 had an essential role in the suppressor function of T cells separable from signaling via the T cell antigen receptor.

DOI10.1038/ni.3540
Alternate JournalNat. Immunol.
PubMed ID27595233
PubMed Central IDPMC5071159
Grant ListP30 CA008748 / CA / NCI NIH HHS / United States
R37 AI034206 / AI / NIAID NIH HHS / United States
/ / Howard Hughes Medical Institute / United States
F30 AI122721 / AI / NIAID NIH HHS / United States
T32 GM007739 / GM / NIGMS NIH HHS / United States
R01 AI107027 / AI / NIAID NIH HHS / United States
P30 CA014195 / CA / NCI NIH HHS / United States

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