Hardwick J C, Ehrlich Y H, Hendley E D
Department of Physiology and Biophysics, University of Vermont College of Medicine, Burlington 05405.
J Neurochem. 1989 Nov;53(5):1512-8. doi: 10.1111/j.1471-4159.1989.tb08546.x.
This study examined the effects of extracellular ATP on norepinephrine (NE) uptake, using PC12 cells as a model of noradrenergic neurons. Previous experiments with synaptosomes led to the hypothesis that extracellular ATP can regulate NE uptake via an ecto-protein kinase. In the present study, we examined the high-affinity uptake of NE (referred to as uptake 1) in PC12 cells in the presence of varying concentrations of extracellular ATP. In the presence of Ca2+, low concentrations of ATP (0.1 microM) increased uptake 1 by approximately 36%. This increase could be mimicked by adenosine-5'-O-(3-thiotriphosphate) tetralithium salt (ATP gamma S), an analogue of ATP which can be utilized by protein kinases, and not by 5'-adenylylimidodiphosphate tetralithium salt, a nonhydrolyzable analogue of ATP, GTP, ADP, and adenosine also had no effect on uptake 1. Preincubation of the cells with NE and ATP gamma S, followed by washing and assaying NE uptake 30 min later, resulted in a persistent increase in uptake 1. Similar pretreatment with ATP did not show this increase; however, simultaneous pretreatment with ATP and ATP gamma S blocked the activation produced by ATP gamma S alone. Kinetic analysis showed that ATP gamma S pretreatment produces an increase in the Vmax of uptake 1 without altering the apparent Km for NE. These results support the hypothesis that extracellular ATP can regulate NE uptake via an ecto-protein kinase.
本研究以PC12细胞作为去甲肾上腺素能神经元模型,研究了细胞外ATP对去甲肾上腺素(NE)摄取的影响。先前对突触体进行的实验提出了一个假设,即细胞外ATP可通过一种胞外蛋白激酶调节NE摄取。在本研究中,我们检测了在不同浓度细胞外ATP存在的情况下,PC12细胞中NE的高亲和力摄取(称为摄取1)。在Ca2+存在的情况下,低浓度的ATP(0.1微摩尔)使摄取1增加了约36%。这种增加可被腺苷-5'-O-(3-硫代三磷酸)四锂盐(ATPγS)模拟,ATPγS是一种ATP类似物,可被蛋白激酶利用,而不能被ATP的非水解类似物5'-腺苷酰亚胺二磷酸四锂盐模拟,GTP、ADP和腺苷对摄取1也没有影响。用NE和ATPγS对细胞进行预孵育,然后洗涤并在30分钟后测定NE摄取,结果导致摄取1持续增加。用ATP进行类似的预处理未显示出这种增加;然而,用ATP和ATPγS同时进行预处理可阻断单独由ATPγS产生的激活作用。动力学分析表明,ATPγS预处理使摄取1的Vmax增加,而不改变NE的表观Km。这些结果支持了细胞外ATP可通过胞外蛋白激酶调节NE摄取这一假设。