Albers, D.; Novikova, S.; Vieyto-Nunez, J.; Almeida-Hernandez, Y.; Pastorio, C.; Klassen, F.; Weiss, D.; von Maltitz, P.; Jaikishan, J.; Datta, M.; Jumaa, H.; Jebaraj, B.; Stilgenbauer, S.; Kumar, M.; Maity, P. C.; Buske, C.; Stifel, U.; Zinngrebe, J.; Fischer-Posovszky, P.; Chevigne, A.; Kirchhoff, F.; Sanchez-Garcia, E.; Muench, J.; Harms, M.

GPR15LG, a chemokine-like ligand for the G-protein coupled receptor 15 (GPR15), is abundantly expressed in the gastrointestinal mucosa and inflamed skin. Emerging evidence suggests its involvement in inflammatory disorders and cancers. This study investigates the effects of GPR15LG on the signaling and downstream functions of C-X-C chemokine receptor type 4 (CXCR4), which plays a critical role in immune cell trafficking and cancer metastasis. The results demonstrate that GPR15LG binds to the orthosteric site of CXCR4, modulating downstream signaling in a context-dependent manner. Specifically, GPR15LG enhances CXCL12-mediated CXCR4 signaling synergistically, promoting wound healing and cell migration across various cell types, including CD4+ T cells and cancer cells. These findings underscore the role of GPR15LG in inflammation and metastasis, offering potential therapeutic avenues for CXCR4-mediated diseases.