Rajendran V M, Binder H J
Department of Internal Medicine, Yale University, New Haven, Connecticut 06510.
J Biol Chem. 1994 Jan 7;269(1):156-60.
This study was designed to investigate the function of intravesicular proton on two pH gradient-dependent transport processes, a novel Na-HCO3 cotransport and a Na-H exchange, that are present in basolateral membrane vesicles of rat distal colon. Increasing intravesicular proton concentration saturated 22Na uptake via both Na-H exchange and Na-HCO3 cotransport; reduced the apparent Km for sodium for Na-H exchange from 94.9 to 35.6 mM, without alteration in the Vmax; but enhanced the Vmax for Na-HCO3 cotransport from 4.3 to 11.7 nmol/mg protein.6 s, while not changing the Km for sodium. The effect of a 10-fold proton concentration gradient at two different absolute proton concentrations on both systems was also determined. 22Na uptake via Na-HCO3 cotransport, but not via Na-H exchange, was enhanced at the higher proton concentration, indicating that the magnitude of the proton concentration gradient is primarily responsible for proton stimulation of Na-H exchange, whereas the absolute proton concentration is critical for proton enhancement of Na-HCO3 cotransport. These studies also demonstrate saturation of both transport systems as a function of intravesicular proton concentration without an exponential component. These results indicate that proton stimulated Na-H exchange and Na-HCO3 cotransport are regulated by distinct and separate mechanisms that may reflect their different cellular functions.
本研究旨在探究膀胱内质子对大鼠远端结肠基底外侧膜囊泡中存在的两种pH梯度依赖性转运过程的作用,这两种转运过程分别是一种新型的Na-HCO₃协同转运和一种Na-H交换。增加囊泡内质子浓度会使通过Na-H交换和Na-HCO₃协同转运的²²Na摄取达到饱和;将Na-H交换中钠的表观Km从94.9 mM降至35.6 mM,而Vmax不变;但会使Na-HCO₃协同转运的Vmax从4.3 nmol/mg蛋白提高到11.7 nmol/mg蛋白.6 s,同时不改变钠的Km。还测定了在两种不同的绝对质子浓度下10倍质子浓度梯度对这两种系统的影响。在较高质子浓度下,通过Na-HCO₃协同转运而非Na-H交换的²²Na摄取增加,这表明质子浓度梯度的大小主要负责质子对Na-H交换的刺激作用,而绝对质子浓度对质子增强Na-HCO₃协同转运至关重要。这些研究还表明,这两种转运系统均随囊泡内质子浓度饱和,且无指数成分。这些结果表明,质子刺激的Na-H交换和Na-HCO₃协同转运受不同且独立的机制调节,这可能反映了它们不同的细胞功能。