Duhm J, Becker B F
J Membr Biol. 1979 Dec 31;51(3-4):263-86. doi: 10.1007/BF01869087.
Ouabain-resistant Na+-Li+ countertransport was studied on erythrocytes of man, sheep, rabbit, and beef. A transport system, exchanging Li+ for Na+ in a ratio of 1:1, was present in all four species. Li+ uptake by the exchange system increased 30-fold in the order man less than HK-sheep less than LK-sheep less than rabbit less than LK-beef. This order is identical to that of ouabain-resistant Na+-Na+ exchange in these species, but bears no relation to the Na+-K+ pump activity. The activity of the Na+-Li+ exchange system varied up to 7 and 16-fold among individual red cell specimens from man and beef, the variability being much smaller in sheep and rabbit erythrocytes. The affinities of the system for Li+ and Na+ were similar among the species and individuals (half saturation of the external site at about 1 mM Li+ and 50 mM Na+, respectively). 50-60% of Na+-Li+ exchange was blocked by N-ethylmaleimide in all species. p-Chloromercuribenzene sulfonate inhibited the exchange only in beef and sheep erythrocytes (60-80%). The two SH-reagents act by decreasing the maximum activity of the system, whilst leaving its affinity for Li+ unaltered. Phloretin was a potent inhibitor in all species. 1 mM each of furosemide, ethacrynic acid, and quinidine induced only a slight inhibition. The Na+-Li+ exchange of human and beef erythrocytes increased 3.5-fold upon elevation of the extracellular pH from 6 to 8.5, the pH-dependence arising from a change in affinity of the system for the cations and being similar to that reported for ouabain-resistant Na+-Na+ exchange in beef erythrocytes. It is concluded that a transport system exists in the red cell membranes of the four species which can mediate ouabain-resistant exchange of either Na+ for Na+, Na+ for Li+, or Li+ for Li+. The exchange system exhibits essentially identical transport characteristics in the four species, but shows a marked inter- and intra-species variability in maximum transport capacity and some differences in susceptibility towards inhibitors. A similar transport system is probably present also in other tissues. The exchange system seems to be distinct from the conventional Na+-K+ pump and shows no clear relation to one of the furosemide-sensitive, ouabain-resistant Na+ transport systems described in the literature.
在人、绵羊、兔和牛的红细胞上研究了哇巴因抗性的钠-锂逆向转运。在所有这四个物种中都存在一种转运系统,该系统以1:1的比例用锂交换钠。通过该交换系统摄取锂的量按照人<高钾绵羊<低钾绵羊<兔<低钾牛的顺序增加了30倍。这个顺序与这些物种中哇巴因抗性的钠-钠交换顺序相同,但与钠-钾泵活性无关。在来自人和牛的单个红细胞标本中,钠-锂交换系统的活性变化高达7倍和16倍,而在绵羊和兔红细胞中的变异性要小得多。该系统对锂和钠的亲和力在物种和个体之间相似(外部位点的半饱和浓度分别约为1 mM锂和50 mM钠)。在所有物种中,50%-60%的钠-锂交换被N-乙基马来酰亚胺阻断。对氯汞苯磺酸盐仅在牛和绵羊红细胞中抑制该交换(60%-80%)。这两种巯基试剂通过降低系统的最大活性起作用,同时不改变其对锂的亲和力。根皮素在所有物种中都是一种有效的抑制剂。1 mM的速尿、依他尼酸和奎尼丁仅引起轻微抑制。当细胞外pH从6升高到8.5时,人和牛红细胞的钠-锂交换增加了3.5倍,pH依赖性源于系统对阳离子亲和力的变化,并且与报道的牛红细胞中哇巴因抗性的钠-钠交换相似。得出的结论是,在这四个物种的红细胞膜中存在一种转运系统,它可以介导钠与钠、钠与锂或锂与锂之间的哇巴因抗性交换。该交换系统在这四个物种中表现出基本相同的转运特性,但在最大转运能力方面表现出明显的种间和种内变异性,并且在对抑制剂的敏感性方面存在一些差异。其他组织中可能也存在类似的转运系统。该交换系统似乎与传统的钠-钾泵不同,并且与文献中描述的一种速尿敏感、哇巴因抗性的钠转运系统没有明显关系。