Villereal M L
J Cell Physiol. 1981 Jun;107(3):359-69. doi: 10.1002/jcp.1041070307.
Human fibroblasts that have been serum deprived for 4 hours have a digitoxin-insensitive Na influx of 9.5 +/- 1.0 (n = 4) mumol/g prot/min which is not significantly different from the influx of 9.4 +/- 0.6 (n = 3) mumol/g prot/min measured in cells arrested in the G1/G0 state by serum-deprivation for a period of four days. The Na influx in serum-deprived cells is rapidly stimulated (within one minute) simply by assaying the cells in medium containing 10% fetal bovine serum (FBS). The digitoxin-insensitive NA influx for cells in the presence of 10% FBS is 22.9 +/- 1.1 (n = 6) mumol/g prot/min. The stimulation of Na influx in serum-deprived cells can also be achieved by the addition of the purified mitogen, epidermal growth factor (EGF). Addition of EGF to serum-deprived cells gives a maximal stimulation of Na influx of approximately 1.6-fold, with the concentration for half-maximal stimulation being 7.5 ng/ml. The stimulation of Na influx results from the activation of an amiloride-sensitive pathway, which appears to be minimally active in serum-deprived cells. Kinetic analysis of Na influx experiments in the presence of 10% FBS and varying concentrations of amiloride indicate that at infinite concentrations of amiloride the Na flux would be reduced to 8.9 mumol/g prot/min, which is comparable to the level of Na flux measured in serum-deprived cells in the presence of 5 mM amiloride. Thus, amiloride can totally inhibit the serum-stimulated component of Na influx while inhibiting less than 10% of the Na influx in serum-deprived cells. The Na influx in serum-deprived cells can also be stimulated 2.5-fold by preincubating cells in the presence of the Ca+ ionophore A23187 to elevate the intracellular Ca content. This stimulation of Na influx by intracellular Ca+2 can be virtually eliminated by adding 1 mM amiloride.
血清饥饿4小时的人成纤维细胞,其对洋地黄毒苷不敏感的钠内流为9.5±1.0(n = 4)μmol/g蛋白/分钟,这与通过血清饥饿4天而停滞在G1/G0期的细胞中测得的9.4±0.6(n = 3)μmol/g蛋白/分钟的内流无显著差异。血清饥饿细胞中的钠内流仅通过在含有10%胎牛血清(FBS)的培养基中检测细胞就能迅速被刺激(在1分钟内)。在10% FBS存在下,细胞对洋地黄毒苷不敏感的钠内流为22.9±1.1(n = 6)μmol/g蛋白/分钟。血清饥饿细胞中钠内流的刺激也可通过添加纯化的促有丝分裂原表皮生长因子(EGF)来实现。向血清饥饿细胞中添加EGF可使钠内流最大刺激约1.6倍,半数最大刺激浓度为7.5 ng/ml。钠内流的刺激是由一种对氨氯地平敏感的途径激活所致,该途径在血清饥饿细胞中似乎活性最低。在10% FBS和不同浓度氨氯地平存在下进行的钠内流实验的动力学分析表明,在氨氯地平无限浓度时,钠通量将降至8.9 μmol/g蛋白/分钟,这与在5 mM氨氯地平存在下血清饥饿细胞中测得的钠通量水平相当。因此,氨氯地平可完全抑制血清刺激的钠内流成分,而抑制血清饥饿细胞中钠内流的比例不到10%。血清饥饿细胞中的钠内流也可通过在Ca+离子载体A23187存在下预孵育细胞以提高细胞内钙含量而被刺激2.5倍。通过添加1 mM氨氯地平,这种由细胞内Ca+2引起的钠内流刺激几乎可被消除。