The Human G Protein-Coupled ATP Receptor P2Y11 Is Associated With IL-10 Driven Macrophage Differentiation

The G protein-coupled P2Y(11) receptor is known to sense extracellular ATP during inflammatory and immune responses. The dinucleotide NAD(+) has also been proposed to be a P2Y(11) receptor ligand but its role is less clear. Here, we have examined for the first time human P2Y(11) receptor protein levels and show that the receptor was upregulated during polarization of M2 macrophages. IL-10 reinforced P2Y(11) receptor expression during differentiation of M2c macrophages expressing CD163, CD16, and CD274 (PD-L1). Nutlin-3a mediated p53 stabilization further increased P2Y(11) receptor, CD16, and PD-L1 expression. AMP-activated kinase (AMPK), which mediates anti-inflammatory effects of IL-10, and nicotinamide phosphoribosyltransferase (NAMPT), the rate-limiting enzyme of the NAD(+) salvage pathway, which is under the control of AMPK, were also required for P2Y(11) receptor expression. The P2Y(11) receptor agonist ATP gamma S and NAD(+) could independently stimulate the production of IL-8 in M2 macrophages, however, only the ATP gamma S-induced response was mediated by P2Y(11) receptor. Both in a recombinant system and in macrophages, P2Y(11) receptor-driven IL-8 production predominantly depended on IkB kinase (IKK), and extracellular signal-regulated kinase (ERK). In conclusion, our data indicate that an AMPK-NAMPT-NAD(+) signaling axis promotes P2Y(11) receptor expression during M2 polarization of human macrophages in response to IL-10. PD-L1 expressing M2c macrophages that secrete the cancer-promoting chemokine IL-8 in response to P2Y(11) receptor stimulation may represent an important target in checkpoint blockade immunotherapy.