Owen N E, Villereal M L
Proc Natl Acad Sci U S A. 1982 Jun;79(11):3537-41. doi: 10.1073/pnas.79.11.3537.
Sodium influx in serum-deprived human diploid fibroblasts can be stimulated by addition of serum (5-fold) or the divalent cation ionophore A23187 (3-fold). The possible involvement of calmodulin in serum or A23187 stimulation of Na+ influx has been investigated by using six psychoactive agents that are known to bind calmodulin and inhibit calmodulin-sensitive enzymes. Each agent inhibited serum- and A23187-stimulated Na+ influx in a dose-dependent manner. Furthermore, the K1 for inhibition of serum-stimulated Na+ influx correlates directly with the Ca2+-specific calmodulin binding previously determined in a cell-free system [Levin, R. M. & Weiss, B. (1979) J. Pharmacol. Exp, Ther. 208, 454--459]. None of the agents tested had any effect on the serum-insensitive component of net Na+ influx in these cells. These data support the concept that serum and A23187 stimulate Na+ influx in human diploid fibroblasts via an increase of intracellular Ca2+ and a subsequent calmodulin-mediated activation of the amiloride-sensitive transport pathway.
血清剥夺的人二倍体成纤维细胞中的钠内流可通过添加血清(5倍)或二价阳离子载体A23187(3倍)来刺激。通过使用六种已知可结合钙调蛋白并抑制钙调蛋白敏感酶的精神活性药物,研究了钙调蛋白在血清或A23187刺激钠内流过程中可能的参与情况。每种药物均以剂量依赖的方式抑制血清和A23187刺激的钠内流。此外,抑制血清刺激的钠内流的K1与先前在无细胞系统中测定的钙特异性钙调蛋白结合直接相关[Levin, R. M. & Weiss, B. (1979) J. Pharmacol. Exp, Ther. 208, 454 - 459]。所测试的药物均对这些细胞中净钠内流的血清不敏感成分没有任何影响。这些数据支持这样一种概念,即血清和A23187通过增加细胞内钙以及随后钙调蛋白介导的氨氯地平敏感转运途径的激活来刺激人二倍体成纤维细胞中的钠内流。