Figure 1 A high level of Ca2+ influx achieved by prolonging the depolarizing pulse abolishes the inhibitory effect of PGE1 on exocytosis. A high level.

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Date of download: 6/25/2016 Copyright © 2016 SPIE. All rights reserved. Expression of channelrhodopsin-2 (ChR2) in layer 5 pyramidal neurons in the barrel.
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Figure 1 A high level of Ca2+ influx achieved by prolonging the depolarizing pulse abolishes the inhibitory effect of PGE1 on exocytosis. A high level of Ca2+ influx achieved by prolonging the depolarizing pulse abolishes the inhibitory effect of PGE1 on exocytosis. Using standard whole-cell capacitance measurements, the exocytosis elicited by depolarizing pulses (from −70 to +10mV) with two different pulse durations was monitored in control and hormone-treated cells. During the depolarizing pulses, the Ca2+ currents were recorded simultaneously. (A and B) The recording traces of ICa and capacitance in control and PGE1-treated cells stimulated with 100- and 500-ms pulses, respectively. The arrows indicate the different experimental conditions. (C) The summaries of capacitance changes (left) and calcium influxes (right) in A and B, control (black), and PGE1 (white). The traces shown in the figure were averaged from 18 to 30 cells. The values of ΔCm and Ca2+ charge integrals were normalized by cell size (fF/pF and pQ/pF). **P<0.01, #NS. Ying Zhao et al. J Endocrinol 2016;229:287-294 © 2016 Society for Endocrinology