Cell Biology International · 2005 · 15 citations · 13 references
Life SciencesCell BiologyPhysiologyCalcium HomeostasisCell SignalingSignal TransductionCalcium MetabolismCalcium SignalingIntracellular Calcium SignalingIon Channel SignalingMembrane ElectrophysiologyCa2+ SignalingCalcium Influx MechanismsCalcium Ion SignalingCalcium Signal TransductionInositol Trisphosphate Receptor SignalingInositol Trisphosphate SignalingIntracellular Calcium DynamicsIntracellular Calcium Release
Human umbilical vein endothelial cells were exposed to sinusoidal electric fields of 0.3 or 30 kV/m, 50 Hz, for 24 h. Changes in intracellular calcium concentration ([Ca(2+)](i)) induced by ATP-stimulation in the absence of extracellular Ca(2+) were observed in individual cells. No differences were observed between the exposure and sham-exposure groups in [Ca(2+)](i) resting level before ATP-stimulation, or in the [Ca(2+)](i) peak levels induced by stimulation. However, the duration of the initial transients in [Ca(2+)](i) following an ATP stimulus was significantly prolonged by exposure to a 30 kV/m field. The inositol trisphosphate receptor inhibitor, xestospongin C, inhibited the ATP-induced elevation in [Ca(2+)](i) in both the exposure and sham-exposure groups. The ATP-receptor P2Y appeared to play an important role in the increase of [Ca(2+)](i). The present results suggest that an extremely low-frequency electric field affects the function of vascular endothelial cells by a mechanism involving activation of P2Y.
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