Nguyen Linh P, Pan Junliang, Dinh Theresa Thanh, Hadeiba Husein, O'Hara Edward, Ebtikar Ahmad, Hertweck Arnulf, Gökmen M Refik, Lord Graham M, Jenner Richard G, Butcher Eugene C, Habtezion Aida
Division of Gastroenterology and Hepatology, Stanford University School of Medicine, Stanford, CA 94305, USA.
The Center for Molecular Biology and Medicine, Veterans Affairs Palo Alto Health Care System and The Palo Alto Veterans Institute for Research, Palo Alto, California 94304, USA.
Nat Immunol. 2015 Feb;16(2):207-213. doi: 10.1038/ni.3079. Epub 2014 Dec 22.
Lymphocyte recruitment maintains intestinal immune homeostasis but also contributes to inflammation. The orphan chemoattractant receptor GPR15 mediates regulatory T cell homing and immunosuppression in the mouse colon. We show that GPR15 is also expressed by mouse TH17 and TH1 effector cells and is required for colitis in a model that depends on the trafficking of these cells to the colon. In humans GPR15 is expressed by effector cells, including pathogenic TH2 cells in ulcerative colitis, but is expressed poorly or not at all by colon regulatory T (Treg) cells. The TH2 transcriptional activator GATA-3 and the Treg-associated transcriptional repressor FOXP3 robustly bind human, but not mouse, GPR15 enhancer sequences, correlating with receptor expression. Our results highlight species differences in GPR15 regulation and suggest it as a potential therapeutic target for colitis.
淋巴细胞募集维持肠道免疫稳态,但也会引发炎症。孤儿趋化因子受体GPR15介导小鼠结肠中调节性T细胞归巢和免疫抑制。我们发现GPR15在小鼠TH17和TH1效应细胞中也有表达,并且在一个依赖于这些细胞向结肠运输的结肠炎模型中,它是结肠炎所必需的。在人类中,GPR15在效应细胞中表达,包括溃疡性结肠炎中的致病性TH2细胞,但在结肠调节性T(Treg)细胞中表达不佳或根本不表达。TH2转录激活因子GATA-3和Treg相关转录抑制因子FOXP3能强烈结合人类而非小鼠的GPR15增强子序列,这与受体表达相关。我们的结果突出了GPR15调控中的物种差异,并表明它是结肠炎的一个潜在治疗靶点。