| Literature DB >> 28900043 |
Thomas Suply1, Sébastien Hannedouche2, Nathalie Carte1, Jianping Li1, Bianka Grosshans1, Michael Schaefer1, Layla Raad1, Valérie Beck1, Solange Vidal1, Agnès Hiou-Feige1, Noémie Beluch1, Samuel Barbieri1, Johann Wirsching1, Nadine Lageyre1, Frank Hillger1, Corinne Debon1, Janet Dawson1, Philip Smith1, Vincent Lannoy2, Michel Detheux2, Francis Bitsch1, Rocco Falchetto1, Tewis Bouwmeester1, Jeffrey Porter3, Birgit Baumgarten1, Keith Mansfield3, José M Carballido1, Klaus Seuwen4, Frédéric Bassilana4.
Abstract
GPR15 is an orphan G protein-coupled receptor (GPCR) that is found in lymphocytes. It functions as a co-receptor of simian immunodeficiency virus and HIV-2 and plays a role in the trafficking of T cells to the lamina propria in the colon and to the skin. We describe the purification from porcine colonic tissue extracts of an agonistic ligand for GPR15 and its functional characterization. In humans, this ligand, which we named GPR15L, is encoded by the gene C10ORF99 and has some features similar to the CC family of chemokines. GPR15L was found in some human and mouse epithelia exposed to the environment, such as the colon and skin. In humans, GPR15L was also abundant in the cervix. In skin, GPR15L was readily detected after immunologic challenge and in human disease, for example, in psoriatic lesions. Allotransplantation of skin from Gpr15l-deficient mice onto wild-type mice resulted in substantial graft protection, suggesting nonredundant roles for GPR15 and GPR15L in the generation of effector T cell responses. Together, these data identify a receptor-ligand pair that is required for immune homeostasis at epithelia and whose modulation may represent an alternative approach to treating conditions affecting the skin such as psoriasis.Entities:
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Year: 2017 PMID: 28900043 DOI: 10.1126/scisignal.aal0180
Source DB: PubMed Journal: Sci Signal ISSN: 1945-0877 Impact factor: 8.192