Yip Kay-Pong, Tsuruoka Shuichi, Schwartz George J, Kurtz Ira
Department of Physiology and Biophysics, College of Medicine, University of South Florida, Tampa, Florida 33612, USA.
Am J Physiol Renal Physiol. 2002 Nov;283(5):F1098-104. doi: 10.1152/ajprenal.0241.2001.
The outer medullary collecting duct (OMCD) plays an important role in mediating transepithelial HCO transport [J(HCO(3)(-))] and urinary acidification. HCO absorption by type A intercalated cells in the OMCD inner stripe (OMCD(is)) segment is thought to by mediated by an apical vacuolar H(+)-ATPase and H(+)-K(+)-ATPase coupled to a basolateral Cl(-)-HCO exchanger (AE1). Besides these Na(+)-independent transporters, previous studies have shown that OMCD(is) type A intercalated cells have an apical electroneutral EIPA-sensitive, DIDS-insensitive Na(+)-HCO cotransporter (NBC3); a basolateral Na(+)/H(+) antiporter; and a basolateral Na(+)-K(+)-ATPase. In this study, we reexamined the Na(+) dependence of transepithelial Na(+) transport in the OMCD(is) and determined the role of apical NBC3 in intracellular (pH(i)) regulation in OMCD(is) type A intercalated cells. Control tubules absorbed HCO at a rate of approximately 13 pmol. min(-1). mm(-1). Lowering luminal Na(+) from 140 to 40 mM decreased [J(HCO(3)(-))] by approximately 15% without a change in transepithelial potential (V(te)). Furthermore, 50 microM EIPA (lumen) also decreased [J(HCO(3)(-))] by approximately 13% without a change in V(te). The effect of lowering luminal Na(+) and adding EIPA were not additive. These results demonstrate that [J(HCO(3)(-))] in the OMCD(is) is in part Na(+) dependent. In separate experiments, the pH(i) recovery rate after an NH prepulse was monitored in single type A intercalated cells with confocal fluorescence microscopy. The pH(i) recovery rate was approximately 0.21 pH/min in Na(+)-containing solutions and decreased to approximately 0.16 pH/min with EIPA (50 microM, lumen). In tubules perfused/bathed without Na(+), luminal Na(+) addition resulted in a pH(i) recovery rate of approximately 0.36 pH/min, whereas the Na(+)-independent recovery rate was approximately 0.16 pH/min. EIPA (50 microM, lumen) decreased the Na(+)-dependent pH(i) recovery rate to approximately 0.07 pH/min. The Na(+)-independent recovery rate was decreased to approximately 0.06 pH/min by bafilomycin (10 nM, lumen) and to approximately 0.10 pH/min using Schering 28080 (10 microM, lumen). These findings indicate that NBC3 contributes to pH(i) regulation in OMCD(is) type A intercalated cells and plays only a minor role in mediating [J(HCO(3)(-))] in the OMCD(is).
外髓集合管(OMCD)在介导跨上皮HCO转运[J(HCO(3)(-))]和尿液酸化过程中发挥着重要作用。OMCD内带(OMCD(is))段A型闰细胞对HCO的吸收被认为是由顶端空泡H(+)-ATP酶和H(+)-K(+)-ATP酶介导的,它们与基底外侧Cl(-)-HCO交换体(AE1)偶联。除了这些不依赖Na(+)的转运体,先前的研究表明,OMCD(is)型A型闰细胞有一个顶端电中性的、对EIPA敏感、对DIDS不敏感的Na(+)-HCO共转运体(NBC3);一个基底外侧Na(+)/H(+)逆向转运体;以及一个基底外侧Na(+)-K(+)-ATP酶。在本研究中,我们重新审视了OMCD(is)中跨上皮Na(+)转运对Na(+)的依赖性,并确定了顶端NBC3在OMCD(is)型A型闰细胞内pH(pH(i))调节中的作用。对照小管以约13 pmol·min(-1)·mm(-1)的速率吸收HCO。将管腔Na(+)浓度从140 mM降至40 mM可使[J(HCO(3)(-))]降低约15%,而跨上皮电位(V(te))无变化。此外,50 μM EIPA(管腔)也可使[J(HCO(3)(-))]降低约13%,而V(te)无变化。降低管腔Na(+)浓度和添加EIPA的作用并非相加的。这些结果表明,OMCD(is)中的[J(HCO(3)(-))]部分依赖于Na(+)。在单独的实验中,用共聚焦荧光显微镜监测单个A型闰细胞在NH预脉冲后的pH(i)恢复率。在含Na(+)的溶液中,pH(i)恢复率约为0.21 pH/min,而加入EIPA(50 μM,管腔)后降至约0.16 pH/min。在无Na(+)灌注/浴的小管中,加入管腔Na(+)可使pH(i)恢复率达到约0.36 pH/min,而不依赖Na(+)的恢复率约为0.16 pH/min。EIPA(50 μM,管腔)可使依赖Na(+)的pH(i)恢复率降至约0.07 pH/min。不依赖Na(+)的恢复率被巴弗洛霉素(10 nM,管腔)降至约0.06 pH/min,使用先灵葆雅28080(10 μM,管腔)后降至约0.10 pH/min。这些发现表明,NBC3有助于OMCD(is)型A型闰细胞中的pH(i)调节,并且在介导OMCD(is)中的[J(HCO(3)(-))]过程中仅起次要作用。