P2Y Receptors Regulate CXCL10 Expression and Secretion in Mouse Intestinal Epithelial Cells.

In this study, we investigated the role of extracellular nucleotides in chemokine (KC, MIP-2, MCP-1, and CXCL10) expression and secretion by murine primary intestinal epithelial cells (IECs) with a focus on P2Y receptors. qRT-PCR experiments showed that P2Y was the dominant nucleotide receptor expressed in mouse IEC. In addition, the P2Y ligand UDP induced expression and secretion of CXCL10. For the other studies, we took advantage of mice deficient in P2Y (). Similar expression levels of P2Y, P2Y, P2X2, P2X4, and A were detected in and WT IEC. Agonists of TLR3 (poly(I:C)), TLR4 (LPS), P2Y, and P2Y increased the expression and secretion of CXCL10 more prominently in IEC than in WT IEC. CXCL10 expression and secretion induced by poly(I:C) in both and WT IEC were inhibited by general P2 antagonists (suramin and Reactive-Blue-2), by apyrase, and by specific antagonists of P2Y, P2Y, P2Y (only in WT), and P2X4. Neither adenosine nor an A antagonist had an effect on CXCL10 expression and secretion. Macrophage chemotaxis was induced by the supernatant of poly(I:C)-treated IEC which was consistent with the level of CXCL10 secreted. Finally, the non-nucleotide agonist FGF2 induced MMP9 mRNA expression also at a higher level in IEC than in WT IEC. In conclusion, extracellular nucleotides regulate CXCL10 expression and secretion by IEC. In the absence of P2Y, these effects are modulated by other P2 receptors also present on IEC. These data suggest that the presence of P2Y regulates chemokine secretion and may also regulate IEC homeostasis.