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The Journal of Neuroscience, October 18, 2006, 26(42):10658-10666; doi:10.1523/JNEUROSCI.2609-06.2006

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Cellular/Molecular
The Orexin OX1 Receptor Regulates Ca2+ Entry via Diacylglycerol-Activated Channels in Differentiated Neuroblastoma Cells

Johnny Näsman,1 Genevieve Bart,1 Kim Larsson,1 Lauri Louhivuori,1 Hanna Peltonen,1 and Karl E. O. Åkerman1,2

1A. I. Virtanen Institute for Molecular Sciences, Department of Neurobiology, University of Kuopio, FIN-70211 Kuopio, Finland, and 2Department of Neuroscience, Uppsala University, Biomedical Center, S-75123 Uppsala, Sweden

Correspondence should be addressed Johnny Näsman, A. I. Virtanen Institute for Molecular Sciences, P.O. Box 1627, FIN-70211 Kuopio, Finland. Email: johnny.nasman{at}uku.fi

We studied the cellular response to orexin type 1 receptor (OX1R) stimulation in differentiated IMR-32 neuroblastoma cells. In vitro differentiation of IMR-32 cells with 5-bromo-2'-deoxyuridine leads to a neuronal phenotype with long neurite extensions and an upregulation of mainly N-type voltage-gated calcium channels. Transduction of differentiated IMR-32 cells with baculovirus harboring an OX1R–green fluorescent protein cDNA fusion construct resulted in appearance of fluorescence that was confined mainly to the plasma membrane in the cell body and to neurites. Application of orexin-A to fluorescent cells led to an increase in intracellular free Ca2+ concentration, [Ca2+]i. At low nanomolar concentrations of orexin-A, the response was reversibly attenuated by removal of extracellular Ca2+, by application of a high concentration (10 mM) of Mg2+, and by the pharmacological channel blocker dextromethorphan. A diacylglycerol, dioctanoylglycerol, but not thapsigargin or depolarization with potassium, mimicked the OX1R response with regard to Mg2+ sensitivity. A reverse transcription-PCR screening identified mRNAs for all transient receptor potential canonical (TRPC) channels, including TRPC3, TRPC6, and TRPC7, which are known to be activated by diacylglycerol. Expression of a dominant-negative TRPC6 channel subunit blunted the responses to both dioctanoylglycerol and OX1R stimulation. The results suggest that the OX1R activates a Ca2+ entry pathway that involves diacylglycerol-activated TRPC channels in neuronal cells.

Key words: baculovirus; calcium; differentiation; neuroblastoma; orexin; TRP channel


Received Oct. 19, 2005; revised Aug. 16, 2006; accepted Aug. 16, 2006.

Correspondence should be addressed Johnny Näsman, A. I. Virtanen Institute for Molecular Sciences, P.O. Box 1627, FIN-70211 Kuopio, Finland. Email: johnny.nasman{at}uku.fi




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