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).
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1 January 1995
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January 01 1995
Measurement of cytosolic Ca2+ concentration in Limulus ventral photoreceptors using fluorescent dyes.
K Y Ukhanov,
K Y Ukhanov
Department of Zoology, University of Maryland, College Park 20742, USA.
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T M Flores,
T M Flores
Department of Zoology, University of Maryland, College Park 20742, USA.
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H S Hsiao,
H S Hsiao
Department of Zoology, University of Maryland, College Park 20742, USA.
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P Mohapatra,
P Mohapatra
Department of Zoology, University of Maryland, College Park 20742, USA.
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C H Pitts,
C H Pitts
Department of Zoology, University of Maryland, College Park 20742, USA.
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R Payne
R Payne
Department of Zoology, University of Maryland, College Park 20742, USA.
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K Y Ukhanov
,
T M Flores
,
H S Hsiao
,
P Mohapatra
,
C H Pitts
,
R Payne
Department of Zoology, University of Maryland, College Park 20742, USA.
Online ISSN: 1540-7748
Print ISSN: 0022-1295
J Gen Physiol (1995) 105 (1): 95–116.
Citation
K Y Ukhanov, T M Flores, H S Hsiao, P Mohapatra, C H Pitts, R Payne; Measurement of cytosolic Ca2+ concentration in Limulus ventral photoreceptors using fluorescent dyes.. J Gen Physiol 1 January 1995; 105 (1): 95–116. doi: https://doi.org/10.1085/jgp.105.1.95
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