Light Dependence of Calcium and Membrane Potential Measured in Blowfly Photoreceptors In Vivo

Light adaptation in insect photoreceptors is caused by an increase in the cytosolic Ca(2+) concentration. To better understand this process, we measured the cytosolic Ca(2+) concentration in vivo as a function of adapting light intensity in the white-eyed blowfly mutant chalky. We developed a technique to measure the cytosolic Ca(2+) concentration under conditions as natural as possible. The calcium indicator dyes Oregon Green 1, 2, or 5N (Molecular Probes, Inc., Eugene, OR) were iontophoretically injected via an intracellular electrode into a photoreceptor cell in the intact eye; the same electrode was also used to measure the membrane potential. The blue-induced green fluorescence of these dyes could be monitored by making use of the optics of the facet lens and the rhabdomere waveguide. The use of the different Ca(2+)-sensitive dyes that possess different affinities for Ca(2+) allowed the quantitative determination of the cytosolic Ca(2+) concentration in the steady state. Determining the cytosolic Ca(2+) concentration as a function of the adapting light intensity shows that the Ca(2+) concentration is regulated in a graded fashion over the whole dynamic range where a photoreceptor cell can respond to light. When a photoreceptor is adapted to bright light, the cytosolic Ca(2+) concentration reaches stable values higher than 10 μM. The data are consistent with the hypothesis that the logarithm of the increase in cytosolic Ca(2+) concentration is linear with the logarithm of the light intensity. From the estimated values of the cytosolic Ca(2+) concentration, we conclude that the Ca(2+)-buffering capacity is limited. The percentage of the Ca(2+) influx that is buffered gradually decreases with increasing Ca(2+) concentrations; at cytosolic Ca(2+) concentration levels above 10 μM, buffering becomes minimal