Prostaglandin E2 promotes intestinal inflammation via inhibiting microbiota-dependent regulatory T cells

被引:51
|
作者
Crittenden, Siobhan [1 ]
Goepp, Marie [1 ]
Pollock, Jolinda [2 ]
Robb, Calum T. [1 ]
Smyth, Danielle J. [3 ]
Zhou, You [4 ,5 ]
Andrews, Robert [4 ,5 ]
Tyrrell, Victoria [4 ,5 ]
Gkikas, Konstantinos [6 ]
Adima, Alexander [1 ]
O'Connor, Richard A. [1 ]
Davies, Luke [4 ,5 ]
Li, Xue-Feng [7 ]
Yao, Hatti X. [1 ]
Ho, Gwo-Tzer [1 ]
Zheng, Xiaozhong [1 ]
Mair, Amil [1 ]
Vermeren, Sonja [1 ]
Qian, Bin-Zhi [7 ]
Mole, Damian J. [1 ]
Gerasimidis, Konstantinos [6 ]
Schwarze, Jurgen K. J. [1 ]
Breyer, Richard M. [8 ,9 ]
Arends, Mark J. [10 ]
O'Donnell, Valerie B. [4 ,5 ]
Iredale, John P. [11 ]
Anderton, Stephen M. [1 ]
Narumiya, Shuh [12 ,13 ]
Maizels, Rick M. [3 ]
Rossi, Adriano G. [1 ]
Howie, Sarah E. [1 ]
Yao, Chengcan [1 ]
机构
[1] Univ Edinburgh, Ctr Inflammat Res, Queens Med Res Inst, Edinburgh EH1 4TJ, Midlothian, Scotland
[2] Scotlands Rural Coll, SRUC Vet Serv, Easter Bush Estate, Aberdeen EH26 0PZ, Scotland
[3] Univ Glasgow, Wellcome Ctr Mol Parasitol, Inst Infect Immun & Inflammat, Glasgow G12 8TA, Lanark, Scotland
[4] Cardiff Univ, Syst Immun Univ Res Inst, Cardiff CF14 4XN, Wales
[5] Cardiff Univ, Div Infect & Immun, Cardiff CF14 4XN, Wales
[6] Univ Glasgow, Sch Med Dent & Nursing, Human Nutr, Glasgow G31 2ER, Lanark, Scotland
[7] Univ Edinburgh, MRC Ctr Reprod Hlth, Queens Med Res Inst, Edinburgh EH16 4TJ, Midlothian, Scotland
[8] Vanderbilt Univ, Med Ctr, Tennessee Valley Hlth Author, Dept Vet Affairs, Nashville, TN USA
[9] Vanderbilt Univ, Med Ctr, Dept Med, Nashville, TN USA
[10] Univ Edinburgh, Canc Res UK Edinburgh Ctr, Inst Genet & Mol Med, Div Pathol, Edinburgh EH4 2XR, Midlothian, Scotland
[11] Univ Bristol, Senate House, Bristol BS8 1TH, Avon, England
[12] Kyoto Univ, Med Innovat Ctr, Alliance Lab Adv Med Res, Grad Sch Med, Kyoto 6068507, Japan
[13] Kyoto Univ, Med Innovat Ctr, Dept Drug Discovery Med, Grad Sch Med, Kyoto 6068507, Japan
基金
欧洲研究理事会; 英国医学研究理事会; 英国惠康基金;
关键词
CHAIN FATTY-ACIDS; DIFFERENTIATION; HOMEOSTASIS; METABOLITES; BACTERIAL; TH17; ACTIVATION; GENERATION; POPULATION; EXPRESSION;
D O I
10.1126/sciadv.abd7954
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The gut microbiota fundamentally regulates intestinal homeostasis and disease partially through mechanisms that involve modulation of regulatory T cells (T-regs), yet how the microbiota-T-reg cross-talk is physiologically controlled is incompletely defined. Here, we report that prostaglandin E-2 (PGE(2)), a well-known mediator of inflammation, inhibits mucosal T(regs )in a manner depending on the gut microbiota. PGE(2) through its receptor EP4 diminishes T-reg-favorable commensal microbiota. Transfer of the gut microbiota that was modified by PGE(2)-EP4 signaling modulates mucosal T-reg responses and exacerbates intestinal inflammation. Mechanistically, PGE(2)-modified microbiota regulates intestinal mononuclear phagocytes and type I interferon signaling. Depletion of mononuclear phagocytes or deficiency of type I interferon receptor diminishes PGE(2)-dependent T(reg )inhibition. Together, our findings provide emergent evidence that PGE(2)-mediated disruption of microbiota-T-reg communication fosters intestinal inflammation.
引用
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页数:16
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