Narayanan N, Su N, Bedard P
Department of Physiology, University of Western Ontario, London, Canada.
Biochim Biophys Acta. 1991 Nov 18;1070(1):83-91. doi: 10.1016/0005-2736(91)90149-3.
While studying the effects of membrane phosphorylation on active Ca2+ transport in cardiac sarcoplasmic reticulum (SR) we used NaF (a conventional phosphatase inhibitor) in the Ca2+ transport assay medium to suppress protein dephosphorylation by endogenous phosphatases. Unexpectedly, depending on the experimental conditions employed, NaF was found to cause a strong inhibitory or stimulatory effect on ATP-dependent, oxalate-facilitated Ca2+ uptake (Ca2+ pump) activity of SR. Investigation of this phenomenon using canine cardiac SR revealed the following. Exposure of SR to NaF in the absence of Ca2+ or ATP in the Ca2+ transport assay medium (prior to initiating Ca2+ transport by the addition of Ca2+ or ATP) promoted a striking concentration-dependent inhibitory effect of NaF (50% and 90% inhibition with approx. 4 and 10 mM NaF, respectively) on Ca2+ uptake by SR; the magnitude of inhibition did not differ appreciably with varying oxalate concentrations. In contrast, exposure of SR to NaF in the presence of both Ca2+ and ATP resulted in a concentration-dependent stimulatory effect of NaF (half-maximal stimulation at approx. 2.5 mM NaF with 2.5 mM oxalate in assay) on Ca2+ uptake; the magnitude of stimulation decreased with increasing oxalate concentration (greater than 2-fold at 1 mM oxalate, 10% at 5 mM oxalate). The inhibitory effect prevailed when SR was exposed to NaF in the presence of Ca2+ alone (without ATP) or ATP alone (without Ca2+). Both the inhibitory and stimulatory effects of NaF were specific to fluoride ion, as NaCl (1-10 mM) showed no effect on Ca2+ uptake by SR under identical assay conditions. A persistently less active state of the Ca2+ pump (evidenced by decreased Ca2+ transport rates) resulted upon pretreatment of SR with NaF in the absence of Ca2+ or ATP; presence of Ca2+ and ATP during pretreatment prevented this transition. The inhibitory action of NaF on the Ca2+ pump was accompanied by a two-fold increase in K0.5 for Ca2+ and decrements in Hill coefficient (nH) and Ca(2+)-stimulated ATP hydrolysis, as well as steady-state level of Ca(2+)-induced phosphoenzyme. The stimulatory effect of NaF, on the other hand, was associated with an increase in the ratio of Ca2+ transported/ATP hydrolysed with only minor changes, if any, in the above parameters. These findings imply that the divergent effects of fluoride are dependent on specific conformational states of the Ca(2+)-ATPase which evolve during the catalytic and ion transport cycle.(ABSTRACT TRUNCATED AT 400 WORDS)
在研究膜磷酸化对心肌肌浆网(SR)中Ca2+主动转运的影响时,我们在Ca2+转运测定培养基中使用了NaF(一种传统的磷酸酶抑制剂)来抑制内源性磷酸酶引起的蛋白质去磷酸化。出乎意料的是,根据所采用的实验条件,发现NaF对SR的ATP依赖性、草酸盐促进的Ca2+摄取(Ca2+泵)活性有强烈的抑制或刺激作用。使用犬心肌SR对这一现象进行研究得到了以下结果。在Ca2+转运测定培养基中,在不存在Ca2+或ATP的情况下(在添加Ca2+或ATP启动Ca2+转运之前)将SR暴露于NaF,会使NaF对SR摄取Ca2+产生显著的浓度依赖性抑制作用(分别用约4 mM和10 mM NaF时抑制50%和90%);抑制程度随草酸盐浓度变化没有明显差异。相反,在同时存在Ca2+和ATP的情况下将SR暴露于NaF,会使NaF对Ca2+摄取产生浓度依赖性刺激作用(在测定中用2.5 mM草酸盐时,约2.5 mM NaF时达到半数最大刺激);刺激程度随草酸盐浓度增加而降低(在1 mM草酸盐时大于2倍,在5 mM草酸盐时为10%)。当SR仅在存在Ca2+(无ATP)或ATP(无Ca2+)的情况下暴露于NaF时,抑制作用占主导。NaF的抑制和刺激作用均对氟离子具有特异性,因为在相同测定条件下,NaCl(1 - 10 mM)对SR摄取Ca2+没有影响。在不存在Ca2+或ATP的情况下用NaF预处理SR会导致Ca2+泵持续处于活性较低的状态(表现为Ca2+转运速率降低);预处理期间存在Ca2+和ATP可防止这种转变。NaF对Ca2+泵的抑制作用伴随着Ca2+的K0.5增加两倍,以及希尔系数(nH)、Ca2+刺激的ATP水解和Ca2+诱导的磷酸酶稳态水平降低。另一方面,NaF的刺激作用与Ca2+转运/ATP水解的比率增加有关,而上述参数仅有微小变化(如果有的话)。这些发现表明,氟化物的不同作用取决于Ca2+ - ATP酶在催化和离子转运循环过程中所呈现的特定构象状态。(摘要截断于400字)