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Peptides. 2008 May;29(5):721-6. doi: 10.1016/j.peptides.2007.12.019. Epub 2008 Jan 31.

State-dependent calcium mobilization by urotensin-II in cultured human endothelial cells.

Author information

1
Department of Pharmacology, 3420 N. Broad Street, Temple University School of Medicine, Philadelphia, PA 19140, USA. ebrailou@temple.edu

Abstract

Human endothelial cells express urotensin-II (U-II) as well as its receptor GPR14. Using microfluorimetric techniques, the effect of human U-II on cytosolic Ca2+ concentrations [Ca2+]i in cultured human aortic endothelial cells (HAECs) loaded with Fura-2 was evaluated in static or flow conditions. Under the static state, U-II (100 nM) abolished spontaneous Ca2+ oscillations, which occurred in a population of cultured HAEC. Similarly, U-II reduced thrombin-, but not ATP-induced calcium responses, suggesting that the peptide does not alter the Gq/11/IP3 pathway; rather, it modifies the coupling between protease-activated receptors and Gq/11/IP3. Under the flow condition, U-II (1, 10 and 100 nM) produced a dose-dependent increase in [Ca2+]i, which was subjected to desensitization. The result demonstrates a state-dependent effect of U-II in cultured HAEC, which may explain the variable responses to U-II under different experimental conditions.

PMID:
18314227
PMCID:
PMC2387077
DOI:
10.1016/j.peptides.2007.12.019
[Indexed for MEDLINE]
Free PMC Article

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