Renal Intercalated Cells Sense and Mediate Inflammation via the P2Y.sub.14 Receptor

• Published in: PloS one 2015-03, Vol.10 (3)
• Main Authors: Azroyan, Anie, Cortez-Retamozo, Virna, Bouley, Richard, Liberman, Rachel, Ruan, Ye Chun, Kiselev, Evgeny, Jacobson, Kenneth A, Pittet, Mikael J, Brown, Dennis, Breton, Sylvie
• Format: Article
• Language: English
• Subjects: B cells; Cellulose; Glucose; Health aspects; Hostages; Inflammation
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0121419

Uncontrolled inflammation is one of the leading causes of kidney failure. Pro-inflammatory responses can occur in the absence of infection, a process called sterile inflammation. Here we show that the purinergic receptor P2Y.sub.14 (GPR105) is specifically and highly expressed in collecting duct intercalated cells (ICs) and mediates sterile inflammation in the kidney. P2Y.sub.14 is activated by UDP-glucose, a damage-associated molecular pattern molecule (DAMP) released by injured cells. We found that UDP-glucose increases pro-inflammatory chemokine expression in ICs as well as MDCK-C11 cells, and UDP-glucose activates the MEK1/2-ERK1/2 pathway in MDCK-C11 cells. These effects were prevented following inhibition of P2Y.sub.14 with the small molecule PPTN. Tail vein injection of mice with UDP-glucose induced the recruitment of neutrophils to the renal medulla. This study identifies ICs as novel sensors, mediators and effectors of inflammation in the kidney via P2Y.sub.14.