TY - JOUR
T1 - GITR controls intestinal inflammation by suppressing IL-15-dependent NK cell activity
AU - Sakurai, Tsuyoshi
AU - Okuyama, Yuko
AU - Kobayashi, Shuhei
AU - Phung, Hai The
AU - Asao, Atsuko
AU - Kawabe, Takeshi
AU - Ndhlovu, Lishomwa C.
AU - Riccardi, Carlo
AU - Kudo, Hironori
AU - Wada, Motoshi
AU - Nio, Masaki
AU - So, Takanori
AU - Ishii, Naoto
N1 - Funding Information:
We thank Shimon Sakaguchi (Osaka University) and Takeshi Takahashi for the gift of the DTA-1 antibody. We also thank the Biomedical Research Core and the Institute for Animal Experimentation (Tohoku University Graduate School of Medicine) for technical support. This work was supported by JSPS KAKENHI Grant Number 16K15508 (NI).
Funding Information:
We thank Shimon Sakaguchi (Osaka University) and Takeshi Takahashi for the gift of the DTA‐1 antibody. We also thank the Biomedical Research Core and the Institute for Animal Experimentation (Tohoku University Graduate School of Medicine) for technical support. This work was supported by JSPS KAKENHI Grant Number 16K15508 (NI).
Publisher Copyright:
© 2020 Federation of American Societies for Experimental Biology
PY - 2020/11/1
Y1 - 2020/11/1
N2 - 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.
AB - 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.
KW - inflammatory bowel disease
KW - innate immunity
KW - natural killer cells
KW - TNFRSF
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U2 - 10.1096/fj.202001675R
DO - 10.1096/fj.202001675R
M3 - Article
C2 - 32910505
AN - SCOPUS:85090440780
SN - 0892-6638
VL - 34
SP - 14820
EP - 14831
JO - FASEB Journal
JF - FASEB Journal
IS - 11
ER -