Dunham Philip B, Kelley Scott J, Logue Paul J
Department of Biology, Syracuse University, 130 College Place, Syracuse, NY 13244-1220, USA.
Am J Physiol Cell Physiol. 2004 Aug;287(2):C336-44. doi: 10.1152/ajpcell.00582.2003. Epub 2004 Apr 7.
Na+/H+ exchangers (NHE) are ubiquitous transporters participating in regulation of cell volume and pH. Cell shrinkage, acidification, and growth factors activate NHE by increasing its sensitivity to intracellular H+ concentration. In this study, the kinetics were studied in dog red blood cells of Na+ influx through NHE as a function of external Na+ concentration (Na+). In cells in isotonic media, Na+ inhibited Na+ influx >40 mM. Osmotic shrinkage activated NHE by reducing this inhibition. In cells in isotonic media + 120 mM sucrose, there was no inhibition, and influx was a hyperbolic function of Na+. The kinetics of Na+-inhibited Na+ influx were analyzed at various extents of osmotic shrinkage. The curves for inhibited Na+ fluxes were sigmoid, indicating more than one Na+ inhibitory site associated with each transporter. Shrinkage significantly increased the Na+ concentration at half-maximal velocity of Na+-inhibited Na+ influx, the mechanism by which shrinkage activates NHE.
钠/氢交换体(NHE)是广泛存在的转运蛋白,参与细胞体积和pH值的调节。细胞收缩、酸化以及生长因子通过提高其对细胞内氢离子浓度的敏感性来激活NHE。在本研究中,以细胞外钠离子浓度(Na⁺)为函数,研究了狗红细胞中通过NHE的钠离子内流动力学。在等渗介质中的细胞中,Na⁺在>40 mM时抑制钠离子内流。渗透性收缩通过减少这种抑制作用来激活NHE。在含有120 mM蔗糖的等渗介质中的细胞中,没有抑制作用,内流是Na⁺的双曲线函数。在不同程度的渗透性收缩下分析了钠离子抑制的钠离子内流动力学。抑制的钠离子通量曲线呈S形,表明每个转运蛋白有不止一个钠离子抑制位点。收缩显著增加了钠离子抑制的钠离子内流半最大速度时的钠离子浓度,这是收缩激活NHE的机制。