| Literature DB >> 29396162 |
Akihiro Shimba1, Guangwei Cui2, Shizue Tani-Ichi3, Makoto Ogawa1, Shinya Abe1, Fumie Okazaki1, Satsuki Kitano4, Hitoshi Miyachi4, Hisakata Yamada5, Takahiro Hara2, Yasunobu Yoshikai5, Takashi Nagasawa6, Günther Schütz7, Koichi Ikuta8.
Abstract
Glucocorticoids are steroid hormones with strong anti-inflammatory and immunosuppressive effects that are produced in a diurnal fashion. Although glucocorticoids have the potential to induce interleukin-7 receptor (IL-7R) expression in T cells, whether they control T cell homeostasis and responses at physiological concentrations remains unclear. We found that glucocorticoid receptor signaling induces IL-7R expression in mouse T cells by binding to an enhancer of the IL-7Rα locus, with a peak at midnight and a trough at midday. This diurnal induction of IL-7R supported the survival of T cells and their redistribution between lymph nodes, spleen, and blood by controlling expression of the chemokine receptor CXCR4. In mice, T cell accumulation in the spleen at night enhanced immune responses against soluble antigens and systemic bacterial infection. Our results reveal the immunoenhancing role of glucocorticoids in adaptive immunity and provide insight into how immune function is regulated by the diurnal rhythm.Entities:
Keywords: CXCR4; T cell; diurnal rhythm; glucocorticoid; interleukin-7
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Year: 2018 PMID: 29396162 DOI: 10.1016/j.immuni.2018.01.004
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745