Inhibition of (interstitial) P2Y 6 receptors attenuates renal fibrosis progression

ABSTRACT Chronic kidney disease (CKD) affects over 850 million people worldwide and is characterized by progressive renal fibrosis driven by activated interstitial fibroblasts. Signaling by extracellular nucleotides and P2 receptors plays an important role in renal pathophysiology, yet its contribution to fibroblast activation and fibrosis remains poorly understood. Here, we investigated the expression and function of G q/11 -coupled P2Y receptors in renal interstitial fibroblasts and their involvement in experimental kidney fibrosis. Using highly selective RNA in situ hybridization, we detected P2Y 1 ( P2ry1 ) and P2Y 6 ( P2ry6 ) receptor expression in interstitial fibroblasts. Notably, P2Y 6 expression was markedly upregulated in several experimental mouse models of renal fibrosis. Functional assays in primary cultured renal fibroblasts confirmed G q/11 -coupled P2Y receptor activity, as evidenced by transient intracellular Ca 2+ elevations upon nucleotide stimulation. Primary cultured renal fibroblasts exhibited enhanced migration in response to extracellular uridine diphosphate (UDP). To assess the contribution of interstitial P2Y 6 receptors to fibrosis progression, we employed an adenine-induced nephropathy model with or without the selective P2Y 6 antagonist MRS2578. Pharmacological inhibition of P2Y 6 significantly reduced the mRNA expression of the myofibroblast marker α-smooth muscle actin and collagen I. Collectively, these findings suggest that upregulated P2Y 6 receptor signaling promotes the transition of resident interstitial cells into myofibroblasts during renal fibrosis, likely by modulating fibroblast migration. Inhibition of P2Y6 signaling could represent a new strategy for reducing excessive renal fibrosis. TRANSLATIONAL STATEMENT This study reveals the role of the P2Y 6 receptor ( P2ry6 ) in fibrotic processes in the kidney. P2Y 6 , a G q/11 protein-coupled UDP-sensitive receptor, is expressed in renal interstitial PDGFR-β-positive cells and macrophages. Its pharmacological inhibition significantly reduces fibrosis in the mouse adenine nephropathy model. Blocking P2Y 6 therefore represents a promising therapeutic strategy for kidney diseases characterized by excessive scarring.