Blaustein M P
Fed Proc. 1976 Dec;35(14):2574-8.
The intracellular ionized calcium concentration ([Ca2+]i) in squid axons is far below that expected at equilibrium, and Ca2+ must therefore be extruded against a large electrochemical gradient in order to maintain the steady state. In the absence of ATP, Ca efflux from internally-dialyzed axons is largely dependent on external Na, and is associated with a Cai-dependent Na influx. An Nai-dependent Ca influx and Cao-dependent Na efflux have also been observed in squid axons. The data imply that the axolemma has a "carrier" mechanism that can mediate the counterflow exchange of Na+ for Ca2+. Several observations indicate that the stoichiometry of the exchange is about 3 Na+-for-1 Ca2+:a) Ca efflux appears to be a cubic function of external Na concentration; b) Ca efflux is reduced when the membrane is depolarized; and c) the Nao-dependent Ca efflux is about 1.5 pmoles/cm2-sec when free [Ca2+]i is about 160 mum, while the Cai-dependent Na influx is about 5 pmoles/cm2sec. If the stoichiometry is 3-for-1, the Na electrochemical gradient, alone, could provide sufficient energy to maintain [Ca2+]i at about 50-200 nM. ATP also influences the Ca efflux: it appears to increase the affinity of the transport mechanism for internal Ca, but does not affect the maximum velocity of transport. Thus ATP may catalyze, but not necessarily energize Ca transport.
枪乌贼轴突内的离子化钙浓度([Ca2+]i)远低于平衡时预期的浓度,因此,为了维持稳态,Ca2+必须逆着较大的电化学梯度被排出。在没有ATP的情况下,从内部透析的轴突中Ca的流出很大程度上依赖于外部的Na,并且与依赖于[Ca]i的Na流入相关。在枪乌贼轴突中也观察到了依赖于[Na]i的Ca流入和依赖于[Ca]o的Na流出。这些数据表明轴膜具有一种“载体”机制,该机制可以介导Na+与Ca2+的逆向交换。一些观察结果表明,这种交换的化学计量比约为3个Na+交换1个Ca2+:a)Ca流出似乎是外部Na浓度的三次函数;b)当膜去极化时,Ca流出减少;c)当游离[Ca2+]i约为160μM时,依赖于[Ca]o的Ca流出约为1.5皮摩尔/平方厘米·秒,而依赖于[Ca]i的Na流入约为5皮摩尔/平方厘米·秒。如果化学计量比是3:1,仅Na电化学梯度就可以提供足够的能量将[Ca2+]i维持在约50 - 200 nM。ATP也影响Ca流出:它似乎增加了转运机制对内部Ca的亲和力,但不影响转运的最大速度。因此,ATP可能催化但不一定为Ca转运提供能量。