Large-conductance channel formation mediated by P2X7 receptor activation is regulated through distinct intracellular signaling pathways in peritoneal macrophages and 2BH4 cells

• Published in: Naunyn-Schmiedeberg's archives of pharmacology Vol. 382; no. 1; pp. 73 - 87
• Main Authors: Faria, R. X., Cascabulho, C. M., Reis, R. A. M., Alves, Luiz Anastácio
• Format: Journal Article
• Language: English
• Published: Berlin/Heidelberg Springer-Verlag 01.07.2010
• Subjects: Adenosine Triphosphate - administration & dosage; Adenosine Triphosphate - metabolism; Animals; Biomedical and Life Sciences; Biomedicine; Cells, Cultured; Flow Cytometry; Ion Channels - metabolism; Macrophages, Peritoneal - metabolism; Mice; Mice, Inbred C57BL; Mitogen-Activated Protein Kinases - metabolism; Neurosciences; Original Article; Patch-Clamp Techniques; Pharmacology/Toxicology; Phosphatidylinositol 3-Kinases - metabolism; Protein Kinase C - metabolism; Receptors, Purinergic P2 - metabolism; Receptors, Purinergic P2X7; Signal Transduction; receptor; Intracellular Ca; Pore formation; P2X; Second messenger
• ISSN: 0028-1298; 1432-1912
• DOI: 10.1007/s00210-010-0523-8

The P2X 7 receptor (P2X7R) is a ligand-gated ATP receptor that acts as a low- and large-conductance channel (pore) and is known to be coupled to several downstream effectors. Recently, we demonstrated that the formation of a large-conductance channel associated with the P2X 7 receptor is induced by increasing the intracellular Ca 2+ concentration (Faria et al., Am J Physiol Cell Physiol 297:C28–C42, 2005 ). Here, we investigated the intracellular signaling pathways associated with P2X 7 large-conductance channel formation using the patch clamp technique in conjunction with fluorescent imaging and flow cytometry assays in 2BH4 cells and peritoneal macrophages. Different antagonists were applied to investigate the following pathways: Ca 2+ -calmodulin, phospholipase A, phospholipase D, phospholipase C, protein kinase C (PKC), mitogen-activated protein kinase (MAPK), MAPK/extracellular signal-regulated kinase, phosphoinositide 3-kinase (PI3K), and cytoskeletal proteins. Macroscopic ionic currents induced by 1 mM ATP were reduced by 85% in the presence of PKC antagonists. The addition of antagonists for MAPK, PI3K, and the cytoskeleton (actin, intermediary filament, and microtubule) blocked 92%, 83%, and 95% of the ionic currents induced by 1 mM ATP, respectively. Our results show that PKC, MAPK, PI3K, and cytoskeletal components are involved in P2X 7 receptor large-channel formation in 2BH4 cells and peritoneal macrophages.