Ukhanov K Y, Flores T M, Hsiao H S, Mohapatra P, Pitts C H, Payne R
Department of Zoology, University of Maryland, College Park 20742, USA.
J Gen Physiol. 1995 Jan;105(1):95-116. doi: 10.1085/jgp.105.1.95.
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).
几种钙敏荧光染料(fura-2、mag-fura-2和钙绿-5N)被用于测量细胞内钙离子浓度(Cai),同时伴随着光诱导的鲎腹神经光感受器的激发。开发了一种比率测量程序用于定量钙绿-5N荧光。将钙绿-5N和一种钙不敏感染料ANTS的混合物注入细胞,并使用两种染料的荧光强度来计算光感受器光敏R叶内Cai的空间平均值。在用fura-2测量时,暗适应光感受器的初始Cai为0.40±0.22微摩尔(标准差,n = 7)。在强烈测量光脉冲开始后700 - 900毫秒时,光敏R叶内的Cai达到峰值,此时用mag-fura-2和钙绿-5N测量时,R叶内Cai的空间平均值分别达到68±14和62±37微摩尔(标准差,n = 5)。在测量条件下,Cai上升速率计算约为350微摩尔/秒。根据mag-fura-2测量结果,Mg2+的静息水平估计为1.9±0.9毫摩尔。为了研究适应光对R叶初始Cai水平的影响,在每次测量前施加1分钟的420纳米背景光脉冲。即使在最低的适应光强度下,即大约每秒传递3×10³个有效光子时,Cai初始水平也出现了第一个显著(P < 0.05)变化。在双对数图上,光适应光感受器的相对敏感性与相对Cai呈线性相关,斜率在 -4.3至 -5.3之间。我们未能检测到光激活受体电位之前的Cai上升。在正常人工海水(ASW)中,室温下用钙绿-5N测量的Cai上升比受体电位开始滞后14±5毫秒(标准差,n = 32)。在无细胞外Ca2+且温度为10℃时,这种滞后增加到44±12毫秒(标准差,n = 17)。