Phaneuf S, Berta P, Casanova J, Cavadore J C
Biochem Biophys Res Commun. 1987 Mar 13;143(2):454-60. doi: 10.1016/0006-291x(87)91375-1.
The effects of extracellular ATP on phosphoinositide metabolism and intracellular Ca2+ concentration were studied in a primary culture of rat aortic myocytes. ATP increases the level of inositol phosphates, the putative second messenger for Ca2+ mobilization. No saturation of inositol phosphates accumulation is obtained (up to 10(-2) M ATP). Under the same conditions, ATP rapidly mobilizes intracellular Ca2+ in fura-2 loaded myocytes. The mobilization of intracellular Ca2+ is dose-dependent (maximal at 10(-4) M ATP), and is not affected by addition of EGTA. It is concluded that the receptors mediating the cytosolic increase of Ca2+ are of the P2-purinoceptor subtype. The physiological functions of these receptors are not presently known.
在大鼠主动脉肌细胞原代培养物中研究了细胞外ATP对磷酸肌醇代谢和细胞内Ca2+浓度的影响。ATP增加了肌醇磷酸的水平,肌醇磷酸是Ca2+动员的假定第二信使。未观察到肌醇磷酸积累的饱和现象(高达10(-2) M ATP)。在相同条件下,ATP能迅速动员负载fura-2的肌细胞内的Ca2+。细胞内Ca2+的动员呈剂量依赖性(在10(-4) M ATP时最大),并且不受EGTA添加的影响。得出的结论是,介导Ca2+胞质增加的受体属于P2-嘌呤能受体亚型。目前尚不清楚这些受体的生理功能。