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Am J Physiol Renal Physiol 279: F92-F101, 2000;
0363-6127/00 $5.00
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Vol. 279, Issue 1, F92-F101, July 2000

Extracellular ATP increases [CA2+]i in distal tubule cells. I. Evidence for a P2Y2 purinoceptor

Michel Bidet, Guy De Renzis, Sonia Martial, Isabelle Rubera, Michel Tauc, and Philippe Poujeol

Unité Mixte de Recherche 6548, Centre National de la Recherche Scientifique Université de Nice-Sophia Antipolis, 06108 Nice Cedex 2, France

Experiments were performed to characterize the P2 purinoceptor subtype responsible for cytoplasmic calcium mobilization in cells from the initial part of rabbit distal convoluted tubule (DCT). Free calcium concentration was measured in a DCT cell line (DC1) with the probe fura 2. Both ATP and UTP increased cytosolic Ca2+ concentration ([Ca2+]i; EC50 3 and 6 µM, respectively). The order of potency for nucleotide analogs was ATP = UTP > adenosine 5'-O-[thiotriphosphate] ADP > UDP, which is consistent with the pharmacology of the P2Y2 receptor subtype. The increased [Ca2+]i responses to ATP and UTP were strongly inhibited by suramin. Pretreatment of cells with pertussis toxin (PTX) attenuated the action of both nucleotides. Inhibition of phospholipase C with U-73122 totally blocked the [Ca2+]i response to ATP. Thus ATP- and UTP-stimulated [Ca2+]i mobilization in DC1 cells appears to be mediated via the activation of P2Y2 purinoceptors coupled to a G protein mechanism that is partially sensitive to PTX. Calcium flux measurements showed that lanthanum- and nifedipine-sensitive calcium channels are involved in the [Ca2+]i response to ATP.

purinergic receptors; kidney; intracellular calcium; calcium channels


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