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

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 T(H)17 and T(H)1 effector cells, an...

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Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4338558/
https://www.ncbi.nlm.nih.gov/pubmed/25531831
http://dx.doi.org/10.1038/ni.3079
Descripción
Sumario: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 T(H)17 and T(H)1 effector cells, and is required for colitis in a model that depends on their trafficking to the colon. In humans GPR15 is expressed by effector cells including pathogenic T(H)2 cells in ulcerative colitis, but is not expressed by regulatory T (T(reg)) cells. The T(H)2 transcriptional activator GATA-3 and the T(reg)–associated transcriptional repressor FOXP3 robustly bind human, but not mouse, GPR15 enhancer sequences, correlating with expression. Our results highlight species differences in GPR15 regulation, and suggest it as a potential therapeutic target for colitis.