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Publication : The P2X7/P2X4 interaction shapes the purinergic response in murine macrophages.

First Author  Pérez-Flores G Year  2015
Journal  Biochem Biophys Res Commun Volume  467
Issue  3 Pages  484-90
PubMed ID  26456657 Mgi Jnum  J:233215
Mgi Id  MGI:5780958 Doi  10.1016/j.bbrc.2015.10.025
Citation  Perez-Flores G, et al. (2015) The P2X7/P2X4 interaction shapes the purinergic response in murine macrophages. Biochem Biophys Res Commun 467(3):484-90
abstractText  The ATP-gated P2X4 and P2X7 receptors are cation channels, co-expressed in excitable and non-excitable cells and play important roles in pain, bone development, cytokine release and cell death. Although these receptors interact the interacting domains are unknown and the functional consequences of this interaction remain unclear. Here we show by co-immunoprecipitation that P2X4 interacts with the C-terminus of P2X7 and by fluorescence resonance energy transfer experiments that this receptor-receptor interaction is driven by ATP. Furthermore, disrupting the ATP-driven interaction by knocking-out P2X4R provoked an attenuation of P2X7-induced cell death, dye uptake and IL-1beta release in macrophages. Thus, P2X7 interacts with P2X4 via its C-terminus and disrupting the P2X7/P2X4 interaction hinders physiological responses in immune cells.
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