GITR controls intestinal inflammation by suppressing IL-15-dependent NK cell activity

Tsuyoshi Sakurai, Yuko Okuyama*, Shuhei Kobayashi, Hai The Phung, Atsuko Asao, Takeshi Kawabe, Lishomwa C. Ndhlovu, Carlo Riccardi, Hironori Kudo, Motoshi Wada, Masaki Nio, Takanori So, Naoto Ishii*

*この論文の責任著者

研究成果: ジャーナルへの寄稿学術論文査読

8 被引用数 (Scopus)

抄録

Glucocorticoid-induced TNFR family related gene (GITR) is a member of the TNFR superfamily that is expressed on cells of the immune system. Although the protective and pathogenic roles of GITR in T cell immunity are well characterized, the role of GITR in innate immunity in the intestinal tissues has not been well clarified. In this study, using a dextran sulfate sodium (DSS)-induced colitis model in mice, we found that GITR-deficiency rendered mice more susceptible to acute intestinal inflammation and that a significantly higher number of activated natural killer (NK) cells was accumulated in the colonic lamina propria of Gitr−/− mice as compared to wild-type mice. Additionally, Rag2−/− Gitr−/− mice, which lack T cells but have NK cells, also displayed more severe colonic inflammation than Rag2−/− mice. In contrast, an anti-GITR agonistic antibody significantly alleviated colitis in Rag2−/− mice. Engagement of GITR inhibited IL-15-mediated activating signaling events in NK cells, which include cell activation and proliferation, and production of cytokines and cytotoxic granules. Taken together, our results provide the first evidence that GITR negatively controls intestinal inflammation through NK cell functions.

本文言語英語
ページ(範囲)14820-14831
ページ数12
ジャーナルFASEB Journal
34
11
DOI
出版ステータス出版済み - 2020/11/01

ASJC Scopus 主題領域

  • バイオテクノロジー
  • 生化学
  • 分子生物学
  • 遺伝学

フィンガープリント

「GITR controls intestinal inflammation by suppressing IL-15-dependent NK cell activity」の研究トピックを掘り下げます。これらがまとまってユニークなフィンガープリントを構成します。

引用スタイル