Helbig H, Korbmacher C, Berweck S, Kühner D, Wiederholt M
Institut für Klinische Physiologie, Klinikum Steglitz der Freien Universität Berlin.
Pflugers Arch. 1988 Jul;412(1-2):80-5. doi: 10.1007/BF00583734.
Uptake studies with 22Na were performed in cultured bovine pigmented ciliary epithelial cells, in order to characterize mechanisms of Na+ transport. A large part of Na+ uptake was sensitive to amiloride, quinidine and harmaline. Na+ uptake was stimulated by intracellular acidification (using the NH+4 prepulse technique), and was inhibited with increasing extracellular proton concentration. Decreasing extracellular pH from 7.5 to 7.0 increased the apparent KM for Na+ from 38 to 86 mM without considerable changes in Vmax. In the presence of 5 mM Na+ half maximal inhibition of amiloride sensitive Na+ uptake by extracellular protons was observed at a hydrogen concentration of 50 nM. In the presence of 50 mM Na+ the proton concentration necessary for 50% inhibition was 139 nM. Thus, the mode of inhibition of extracellular H+ seemed to be competitive with a Ki of 20-40 nM. 10 microM amiloride increased the apparent KM for Na+ from 33 mM to 107 mM, while Vmax remained nearly unchanged. IC50 for amiloride was 6 microM at 5 mM Na+ and 36 microM in the presence of 150 mM Na+. Thus, amiloride behaves as a competitive inhibitor with a Ki of about 5 microM. The affinities of Na+ to the transport site (KM approximately 16 mM), to the inhibitory site for protons (KM approximately 21 mM), and to the inhibitory site for amiloride (KM approximately 26 mM) were in the same order of magnitude. In summary, we have presented evidence for the presence of a Na+/H+ exchanger in cultured bovine pigmented ciliary epithelial cells.(ABSTRACT TRUNCATED AT 250 WORDS)
为了表征钠离子转运机制,我们在培养的牛色素性睫状上皮细胞中进行了用22Na的摄取研究。大部分钠离子摄取对氨氯吡脒、奎尼丁和骆驼蓬碱敏感。钠离子摄取受到细胞内酸化(使用NH+4预脉冲技术)的刺激,并随着细胞外质子浓度的增加而受到抑制。将细胞外pH从7.5降至7.0会使钠离子的表观KM从38 mM增加到86 mM,而Vmax没有显著变化。在存在5 mM钠离子的情况下,在氢浓度为50 nM时观察到细胞外质子对氨氯吡脒敏感的钠离子摄取的半数最大抑制。在存在50 mM钠离子的情况下,50%抑制所需的质子浓度为139 nM。因此,细胞外H+的抑制模式似乎是竞争性的,Ki为20 - 40 nM。10 microM氨氯吡脒使钠离子的表观KM从33 mM增加到107 mM,而Vmax几乎保持不变。在5 mM钠离子存在下氨氯吡脒的IC50为6 microM,在150 mM钠离子存在下为36 microM。因此,氨氯吡脒表现为竞争性抑制剂,Ki约为5 microM。钠离子对转运位点(KM约为16 mM)、质子抑制位点(KM约为21 mM)和氨氯吡脒抑制位点(KM约为26 mM)的亲和力处于相同数量级。总之,我们提供了证据表明在培养的牛色素性睫状上皮细胞中存在钠/氢交换器。(摘要截断于250字)