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Role and species-specific expression of colon T cell homing receptor GPR15 in colitis

2014; Nature Portfolio; Volume: 16; Issue: 2 Linguagem: Inglês

10.1038/ni.3079

1529-2916

Linh P. Nguyen, Junliang Pan, Thanh Theresa Dinh, Husein Hadeiba, Edward O’Hara, Ahmad Ebtikar, Arnulf Hertweck, Refik Gökmen, Graham M. Lord, Richard G. Jenner, Eugene C. Butcher, Aida Habtezion,

Immune Response and Inflammation

The chemoattractant receptor GPR15 can direct CD4+ T cells to the colon. Habtezion and colleagues show that GATA-3 and Foxp3 exhibit species-specific differences in promoting GPR15 expression and thereby influences homing of CD4+ effector and regulatory T cells. 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.