Measurement of cytosolic Ca2+ concentration in Limulus ventral photoreceptors using fluorescent dyes.
Open Access
- 1 January 1995
- journal article
- Published by Rockefeller University Press in The Journal of general physiology
- Vol. 105 (1) , 95-116
- https://doi.org/10.1085/jgp.105.1.95
Abstract
Several Ca-sensitive fluorescent dyes (fura-2, mag-fura-2 and Calcium Green-5N) were used to measure intracellular calcium ion concentration, Cai, accompanying light-induced excitation of Limulus ventral nerve photoreceptors. A ratiometric procedure was developed for quantification of Calcium Green-5N fluorescence. A mixture of Calcium Green-5N and a Ca-insensitive dye, ANTS, was injected in the cell and the fluorescence intensities of both dyes were used to calculate the spatial average of Cai within the light-sensitive R lobe of the photoreceptor. In dark-adapted photoreceptors, the initial Cai was 0.40 +/- 0.22 microM (SD, n = 7) as measured with fura-2. Cai peaked in the light-sensitive R lobe at 700-900 ms after the onset of an intense measuring light step, when the spatial average of Cai within the R lobe reached 68 +/- 14 and 62 +/- 37 microM (SD, n = 5) as measured with mag-fura-2 and Calcium Green-5N, respectively. The rate of Cai rise was calculated to be approximately 350 microM/s under the measuring conditions. The resting level of Mg2+ was estimated to be 1.9 +/- 0.9 mM, calculated from mag-fura-2 measurements. To investigate the effect of adapting light on the initial Cai level in the R lobe, a 1-min step of 420 nm background light was applied before each measurement. The first significant (P < 0.05) change in the initial level of Cai occurred even at the lowest adapting light intensity, which delivered approximately 3 x 10(3) effective photons/s. The relative sensitivity of the light-adapted photoreceptors was linearly related to the relative Cai on a double log plot with slope between -4.3 and -5.3. We were unable to detect a Cai rise preceding the light-activated receptor potential. The Cai rise, measured with Calcium Green-5N, lagged 14 +/- 5 ms (SD, n = 32) behind the onset of the receptor potential at room temperature in normal ASW. In the absence of extracellular Ca2+ and at 10 degrees C, this lag increased to 44 +/- 12 ms (SD, n = 17).Keywords
This publication has 36 references indexed in Scilit:
- A new generation of Ca2+ indicators with greatly improved fluorescence properties.Published by Elsevier ,2021
- Ca2+ is an obligatory intermediate in the excitation cascade of limulus photoreceptorsNeuron, 1993
- Photoreceptor excitation and adaptation by inositol 1,4,5-trisphosphateNature, 1984
- Quantitative pressure injection of picoliter volumes into Limulus ventral photoreceptorsBiophysical Journal, 1983
- Distinct lobes of Limulus ventral photoreceptors. II. Structure and ultrastructure.The Journal of general physiology, 1982
- Ca2+-sequestering smooth endoplasmic reticulum in an invertebrate photoreceptor. II. Its properties as revealed by microphotometric measurements.The Journal of cell biology, 1982
- Re-Examination of the Apparent Binding Constant of Ethylene Glycol Bis(β-Aminoethyl Ether)-N,N,N',N'-Tetraacetic Acid with Calcium around Neutral pH12The Journal of Biochemistry, 1980
- Detection of light‐induced changes of intracellular ionized calcium concentration in Limulus ventral photoreceptors using arsenazo IIIThe Journal of Physiology, 1977
- Changes in Intracellular Free Calcium Concentration during Illumination of Invertebrate PhotoreceptorsThe Journal of general physiology, 1974
- The Effects of Intracellular Iontophoretic Injection of Calcium and Sodium Ions on the Light Response of Limulus Ventral PhotoreceptorsThe Journal of general physiology, 1972