Jacobs W R, Mandel L J
J Membr Biol. 1987;97(1):53-62. doi: 10.1007/BF01869614.
Sodium-calcium exchange has been suggested to play a pivotal role in the regulation of cytosolic free calcium (Caf) by epithelial cells. Using isolated epithelial cells from the toad urinary bladder, Caf has been measured using the intracellular Ca-sensitive fluorescent dyes Fura 2 and Quin 2. Dye loading did not alter cell viability as assessed by measurements of ATP and ADP content or cell oxygen consumption. When basal Caf was examined over a wide range of cell dye content (from 0.04 to 180 nmol dye/mg protein) an inverse relationship was observed. At low dye content, Caf was 300-380 nM and, as dye content was increased, Caf progressively fell to 60 nM. Using low dye content cells, in which minimal alteration in Ca steady state would be expected, the role for plasma membrane Na-Ca exchange was examined using either medium sodium substitution or ouabain. While medium sodium substitution increased Caf, prolonged treatment with ouabain had no effect on Caf despite a clear increase in cell sodium content. The lack of effect of ouabain suggests that Na-Ca exchange-mediated Ca efflux plays a minimal role in the regulation of basal Caf. However, exchange-mediated Ca efflux may play a role in Caf regulation when cytosolic calcium is elevated.
钠钙交换被认为在上皮细胞调节胞质游离钙(Caf)中起关键作用。利用从蟾蜍膀胱分离出的上皮细胞,使用细胞内钙敏感荧光染料Fura 2和Quin 2测量Caf。通过测量ATP和ADP含量或细胞氧消耗评估,染料加载并未改变细胞活力。当在广泛的细胞染料含量范围(从0.04到180 nmol染料/毫克蛋白质)内检测基础Caf时,观察到一种反比关系。在低染料含量时,Caf为300 - 380 nM,随着染料含量增加,Caf逐渐降至60 nM。使用低染料含量细胞(预期钙稳态变化最小),通过培养基钠替代或哇巴因研究质膜钠钙交换的作用。虽然培养基钠替代增加了Caf,但尽管细胞钠含量明显增加,长时间用哇巴因处理对Caf没有影响。哇巴因缺乏作用表明钠钙交换介导的钙外流在基础Caf调节中起最小作用。然而,当胞质钙升高时,交换介导的钙外流可能在Caf调节中起作用。