Schild L, Aronson P S, Giebisch G
Department of Cellular and Molecular Physiology, Yale University School of Medicine, New Haven, Connecticut 06510.
Am J Physiol. 1990 Mar;258(3 Pt 2):F530-6. doi: 10.1152/ajprenal.1990.258.3.F530.
We used real-time recordings of cell volume changes to test for the role of the Cl(-)-formate exchanger in mediating NaCl entry across the apical membrane of rabbit proximal tubule cells. In the absence of extracellular Cl-, 0.5 and 5 mM formate in the tubule lumen induced an increase in cell volume of 1 and 9%, respectively. Formate-induced cell swelling was reduced by alkalinizing the tubule lumen or by addition of luminal amiloride (2 mM), indicating that the increase in cell volume results from the intracellular accumulation of Na-formate via nonionic diffusion of formic acid in parallel with Na(+)-H+ exchange. The cell volume increase induced by 0.5 mM formate was potentiated (from 1 to 4%) by Cl-, as expected for a formate-mediated stimulation of NaCl uptake via parallel Cl(-)-formate exchange and Na(+)-H+ exchange across the apical membrane. By contrast, the cell volume increase induced by 5 mM formate was attenuated (from 9 to 4%) by Cl-. The attenuating effect of Cl- on formate-induced cell swelling required the operation of the apical membrane Cl(-)-formate exchanger. The effect of 1:1 Cl(-)-formate exchange to attenuate formate-induced cell swelling can be explained if the cell possesses a volume-activated anion exit pathway, most likely at the basolateral cell membrane, that is capable of mediating the efflux of Cl- but not formate from the cell.
我们使用细胞体积变化的实时记录来测试Cl(-)-甲酸根交换体在介导NaCl跨兔近端小管细胞顶端膜进入细胞过程中的作用。在无细胞外Cl-的情况下,小管腔内0.5 mM和5 mM的甲酸根分别使细胞体积增加了1%和9%。通过使小管腔碱化或添加管腔阿米洛利(2 mM)可减少甲酸根诱导的细胞肿胀,这表明细胞体积增加是由于甲酸通过与Na(+)-H+交换平行的非离子扩散在细胞内积累形成甲酸钠所致。正如通过顶端膜上平行的Cl(-)-甲酸根交换和Na(+)-H+交换介导的甲酸根刺激NaCl摄取所预期的那样,0.5 mM甲酸根诱导的细胞体积增加被Cl-增强(从1%增加到4%)。相比之下,5 mM甲酸根诱导的细胞体积增加被Cl-减弱(从9%降至4%)。Cl-对甲酸根诱导的细胞肿胀的减弱作用需要顶端膜Cl(-)-甲酸根交换体的参与。如果细胞具有一个体积激活的阴离子流出途径,最有可能位于基底外侧细胞膜,该途径能够介导Cl-而非甲酸根从细胞中流出,那么1:1的Cl(-)-甲酸根交换减弱甲酸根诱导的细胞肿胀的作用就可以得到解释。