Abstract
Salivary glands express multiple isoforms of P2X and P2Y nucleotide receptors, but their in vivo physiological roles are unclear. P2 receptor agonists induced salivation in an ex vivo submandibular gland preparation. The nucleotide selectivity sequence of the secretion response was BzATP ≫ ATP > ADP ≫ UTP, and removal of external Ca2+ dramatically suppressed the initial ATP-induced fluid secretion (∼85%). Together, these results suggested that P2X receptors are the major purinergic receptor subfamily involved in the fluid secretion process. Mice with targeted disruption of the P2X7 gene were used to evaluate the role of the P2X7 receptor in nucleoti-de-evoked fluid secretion. P2X7 receptor protein and BzATP-activated inward cation currents were absent, and importantly, purinergic receptor agonist-stimulated salivation was suppressed by more than 70% in submandibular glands from P2X7-null mice. Consistent with these observations, the ATP-induced increases in [Ca2+]i were nearly abolished in P2X7-/- submandibular acinar and duct cells. ATP appeared to also act through the P2X7 receptor to inhibit muscarinic-induced fluid secretion. These results demonstrate that the ATP-sensitive P2X7 receptor regulates fluid secretion in the mouse submandibular gland. © 2009 by The American Society for Biochemistry and Molecular Biology, Inc.
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CITATION STYLE
Nakamoto, T., Brown, D. A., Catalán, M. A., Gonzalez-Begne, M., Romanenko, V. G., & Melvin, J. E. (2009). Purinergic P2X7 receptors mediate ATP-induced saliva secretion by the mouse submandibular gland. Journal of Biological Chemistry, 284(8), 4815–4822. https://doi.org/10.1074/jbc.M808597200
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