Valant P A, Adjei P N, Haynes D H
Department of Molecular and Cellular Pharmacology, University of Miami School of Medicine, Florida 33101.
J Membr Biol. 1992 Oct;130(1):63-82. doi: 10.1007/BF00233739.
This communication reports the kinetics of the Na+/Ca2+ exchanger and of the plasma membrane (PM) Ca2+ pump of the intact human platelet. The kinetic properties of these two systems were deduced by studying the rate of Ca2+ extrusion and its Na+ dependence for concentrations of cytoplasmic free Ca2+ ([Ca2+]cyt) in the 1-10-microM range. The PM Ca(2+)-ATPase was previously characterized (Johansson, J.S. Haynes, D.H. 1988. J. Membrane Biol. 104:147-163) for [Ca2+]cyt < or = 1.5 microM with the fluorescent Ca2+ indicator quin2 (Kd = 115 nM). That study determined that the PM Ca2+ pump in the basal state has a Vmax = 0.098 mM/min, a Km = 80 nM and a Hill coefficient = 1.7. The present study extends the measurable range of [Ca2+]cyt with the intracellular Ca2+ probe, rhod2 (Kd = 500 nM), which has almost a fivefold lower affinity for Ca2+. An Appendix also describes the Mg2+ and pH dependence of the Kd and fluorescence characteristics of the commercially available dye, which is a mixture of two molecules. Rates of active Ca2+ extrusion were determined by two independent methods which gave good agreement: (i) by measuring Ca2+ extrusion into a Ca(2+)-free medium (above citation) or (ii) by the newly developed "ionomycin short-circuit" method, which determines the ionomycin concentration necessary to short circuit the PM Ca2+ extrusion systems. Absolute rates of extrusion were determined by knowledge of how many Ca2+ ions are moved by ionomycin per minute. The major findings are as follows: (i) The exchanger is saturable with respect to Ca2+ with a Km = 0.97 +/- 0.31 microM and Vmax = 1.0 +/- 0.6 mM/min. (ii) At high [Ca2+]cyt, the exchanger works at a rate 10 times as large as the basal Vmax of the PM Ca2+ extrusion pump. (iii) The exchanger can work in reverse after Na+ loading of the cytoplasm by monensin. (iv) The PM Ca2+ extrusion pump is activated by exposure to [Ca2+]cyt > or = 1.5 microM for 20-50 sec. Activation raises the pump Vmax to 1.6 +/- 0.6 mM/min and the Km to 0.55 +/- 0.24 microM. (v) The Ca2+ buffering capacity of the cytoplasm is 3.6 mM in the 0.1 to 3 microM range of [Ca2+]cyt. In summary, the results show that the human platelet can extrude Ca2+ very rapidly at high [Ca2+]cyt. Both the Na+/Ca2+ exchanger and Ca2+ pump activation may prevent inappropriate platelet activation by marginal stimuli.
本通讯报道了完整人血小板中钠钙交换体和质膜(PM)钙泵的动力学。通过研究1 - 10微摩尔范围内细胞质游离钙浓度([Ca2+]cyt)下的钙外排速率及其对钠的依赖性,推导了这两个系统的动力学特性。先前已用荧光钙指示剂喹啉2(Kd = 115 nM)对[Ca2+]cyt≤1.5微摩尔时的PM钙ATP酶进行了表征(约翰松,J.S. 海恩斯,D.H. 1988.《膜生物学杂志》104:147 - 163)。该研究确定基础状态下的PM钙泵Vmax = 0.098毫摩尔/分钟,Km = 80 nM,希尔系数 = 1.7。本研究使用细胞内钙探针罗丹明2(Rhod2,Kd = 500 nM,对钙的亲和力几乎低五倍)扩展了[Ca2+]cyt的可测量范围。附录还描述了市售染料(两种分子的混合物)的Kd和荧光特性对镁和pH的依赖性。通过两种独立方法确定了活性钙外排速率,二者结果吻合良好:(i)通过测量钙向无钙培养基中的外排(上述引用文献),或(ii)通过新开发的“离子霉素短路”方法,该方法确定使PM钙外排系统短路所需的离子霉素浓度。通过了解离子霉素每分钟移动的钙离子数量确定了绝对外排速率。主要发现如下:(i)交换体对钙具有饱和性,Km = 0.97±0.31微摩尔,Vmax = 1.0±0.6毫摩尔/分钟。(ii)在高[Ca2+]cyt时,交换体的工作速率是PM钙外排泵基础Vmax的10倍。(iii)通过莫能菌素使细胞质钠负载后,交换体可逆向工作。(iv)暴露于[Ca2+]cyt≥1.5微摩尔20 - 50秒可激活PM钙外排泵。激活后泵的Vmax升至1.6±0.6毫摩尔/分钟,Km升至0.55±0.24微摩尔。(v)在[Ca2+]cyt为0.1至3微摩尔范围内,细胞质的钙缓冲能力为3.6毫摩尔。总之,结果表明人血小板在高[Ca2+]cyt时能非常快速地外排钙。钠钙交换体和钙泵的激活均可能通过边缘刺激防止血小板不适当激活。