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J Physiol Volume 560, Number 2, 505-517, October 15, 2004 DOI: 10.1113/jphysiol.2004.068924
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Quantal release of ATP from clusters of PC12 cells

Alessandra Fabbro1,2, Andrei Skorinkin3, Micaela Grandolfo1, Andrea Nistri1,2 and Rashid Giniatullin1,2,4

1 Sector of Neurobiology
2 INFM Unit, International School for Advanced Studies (SISSA), 34014 Trieste, Italy
3 Biochemical and Biophysical Institute of the Russian Academy of Sciences, 420008 Kazan, Russia
4 Kazan Medical University, 420012 Kazan, Russia

Although ATP is important for intercellular communication, little is known about the mechanism of endogenous ATP release due to a dearth of suitable models. Using PC12 cells known to express the P2X2 subtype of ATP receptors and to store ATP with catecholamines inside dense-core vesicles, we found that clusters of PC12 cells cultured for 3–7 days generated small transient inward currents (STICs) after an inward current elicited by exogenous ATP. The amplitude of STICs in individual cells correlated with the peak amplitude of ATP-induced currents. STICs appeared as asynchronous responses (approximately 20 pA average amplitude) for 1–20 s and were investigated with a combination of patch clamping, Ca2+ imaging, biochemistry and electron microscopy. Comparable STICs were produced by focal KCl pulses and were dependent on extracellular Ca2+. STICs were abolished by the P2X antagonist PPADS and potentiated by Zn2+, suggesting they were mediated by P2X2 receptor activation. The highest probability of observing STICs was after the peak of intracellular Ca2+ increase caused by KCl. Biochemical measurements indicated that KCl application induced a significant release of ATP from PC12 cells. Electron microscopy studies showed narrow clefts without ‘synaptic-like’ densities between clustered cells. Our data suggest that STICs were caused by quantal release of endogenous ATP by depolarized PC12 cells in close juxtaposition to the recorded cell. Thus, STICs may be a new experimental model to characterize the physiology of vesicular release of ATP and to study the kinetics and pharmacology of P2X2 receptor-mediated quantal currents.

(Received 26 May 2004; accepted after revision 23 August 2004; first published online 26 August 2004)
Corresponding author A. Nistri: Sector of Neurobiology, International School for Advanced Studies (SISSA), 34014 Trieste, Italy. Email: nistri{at}sissa.it




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