Ca 2+ oscillations induced by histamine H 1 receptor stimulation in HeLa cells: Fura-2 and patch clamp analysis

Abstract

The response of HeLa cells to histamine H 1 receptor stimulation is characterized by periodic increases in cytosolic free Ca 2+ concentration. The mechanisms underlying this oscillatory behaviour are not well understood. Fura-2 and patch clamp experiments carried out on HeLa cells have previously shown: (a) that Ca 2+ oscillations are not initially dependent on the presence of external Ca 2+, that external Ca 2+ is required to maintain the oscillatory activity; (b) that a depolarization of the cell membrane leads to an inhibition of Ca 2+ oscillations during the external Ca 2+ dependent phase of the process; and (c) that Ca 2+ oscillations can be abolished during this latter phase by the exogenous addition of Ca 2+ channel blocking agents, such as Co 2+ or La 3+. The contribution of the inositol phosphate pathway to Ca 2+ oscillations was more recently investigated in whole cell experiments performed with patch pipettes containing IP 3 or the non-hydrolysable GTP analogue GTP-γS. Clear periodic current fluctuations were recorded using both patch pipette solutions. Assuming that the intracellular IP 3 level remained constant under these conditions, these findings provide direct evidence that the Ca 2+ oscillations in HeLa cells do not arise from a periodic production of IP 3. The effect of the internal and external cell pri on the oscillatory process was also investigated in Fura-2 and patch clamp experiments. It was found that an increase in intracellular pH from 7.4 to 7.7 during the external Ca 2+ dependent phase of the histamine stimulation abolishes the appearance of Ca 2+ spikes whereas, a cellular acidification to pH 7.2 maintains or stimulates the Ca 2+ oscillatory activity. The former effect was observed in the absence of Ca 2+ in the bathing medium, indicating that the inhibitory action of alkaline pH was not related to a reduced Ca 2+ entry. An increase in extracellular pH from 7.3 to 9.0 in contrast elicited an intracellular Ca 2+ accumulation which resulted in most cases in an inhibition of the oscillatory process. This effect was dependent on external Ca 2+ and was observed in alkaline internal pH conditions (pH 7.7). These observations suggest: (a) that the net Ca 2+ influx in HeLa cells is strongly dependent on the cell internal and external pH; and (b) that the magnitude of this Ca 2+ influx controls to a large extent the oscillation frequency. Finally, an inhibition of the histamine induced Ca 2+ oscillatory activity was observed following the addition of the Ca 2+-induced Ca 2+-release (CICR) inhibitor adenine to the external medium. This finding indicates that there is a possible contribution of a CICR mechanism to the Ca 2+ oscillations in HeLa cells. A similar inhibitory action of adenine was also observed in the absence of Ca 2+ in the bathing solution. These observations tend therefore to support a model in which Ca 2+ oscillations are related to a CICR mechanism fueled by a pH dependent net Ca 2+ influx.