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Am J Physiol Gastrointest Liver Physiol 289: G935-G948, 2005. First published May 19, 2005; doi:10.1152/ajpgi.00017.2005
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HORMONES AND SIGNALING

P2X2 receptors are essential for [Ca2+]i increases in response to ATP in cultured rat myenteric neurons

Toshio Ohta, Akane Kubota, Matsuka Murakami, Ken-ichi Otsuguro, and Shigeo Ito

Laboratory of Pharmacology, Department of Biomedical Science, Graduate School of Veterinary Medicine, Hokkaido University, Sapporo, Japan

Submitted 29 March 2005 ; accepted in final form 25 July 2005

We characterized ATP-induced changes in intracellular Ca2+ concentration ([Ca2+]i) and membrane current in cultured rat myenteric neurons using ratiometric Ca2+ imaging with fura-2 and the whole cell patch-clamp technique, respectively. Neuronal cells were functionally identified by [Ca2+]i responses to high K+ and nicotine, which occurred only in cells positive for neuron-specific protein gene product 9.5 immunoreactivity. ATP evoked a dose-dependent increase of [Ca2+]i that was greatly decreased by the removal of extracellular Ca2+ concentration ([Ca2+]o). The amplitude of the [Ca2+]i response to ATP was reduced by half in the presence of voltage-dependent Ca2+ channel blockers. In [Ca2+]o-free solution, ATP produced a small transient rise in [Ca2+]i similar to that induced by P2Y agonists. At –60 mV, ATP evoked a slowly inactivating inward current that was suppressed by the removal of extracellular Na+ concentration. The current-voltage relation for ATP showed an inward rectification with the reversal potential of about 0 mV. The apparent rank order of potency for the purinoceptor agonist-induced increases of [Ca2+]i was ATP ≥ adenosine 5'-O-3-triphosphate ≥ CTP ≥ 2-methylthio-ATP > benzoylbenzoyl-ATP. A similar potency order was obtained with current responses to these agonists. P2 antagonists inhibited inward currents induced by ATP. Ca2+ and Mg2+ suppressed the ATP-induced current, and Zn2+, Cu2+, and protons potentiated it. RT-PCR and immunocytochemical studies showed the expression of P2X2 receptors in cultured rat myenteric neurons. These results suggest that ATP mainly activates ionotropic P2X2 receptors, resulting in a [Ca2+]i increase dependent on [Ca2+]o in rat myenteric neurons. A small part of the ATP-induced [Ca2+]i increase may be also mediated via a P2Y receptor-related mechanism.

enteric neuron; fura-2; patch clamp; purinoceptor



Address for reprint requests and other correspondence: T. Ohta, Laboratory of Pharmacology, Dept. of Biomedical Science, Graduate School of Veterinary Medicine, Hokkaido Univ., Sapporo 060-0818 Japan (e-mail: tohta{at}vetmed.hokudai.ac.jp)




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