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大鼠肺泡上皮细胞中Na(+)-H+逆向转运活性的极化分布。

Polarized distribution of Na(+)-H+ antiport activity in rat alveolar epithelial cells.

作者信息

Lubman R L, Crandall E D

机构信息

Division of Pulmonary and Critical Care Medicine, University of Southern California, Los Angeles 90033.

出版信息

Am J Physiol. 1994 Feb;266(2 Pt 1):L138-47. doi: 10.1152/ajplung.1994.266.2.L138.

Abstract

In this study, we investigated the polarized distribution of Na(+)-H+ antiport activity in alveolar epithelial cell monolayers. Rat alveolar type II pneumocytes were grown on detachable tissue culture-treated Nuclepore filters. The membrane filters, with their adherent intact alveolar epithelial cell monolayers, were mounted in a cuvette designed to contain two fluid compartments separated by the monolayer. Cells were loaded with the pH-sensitive dye 2',7'-biscarboxyethyl-5,6-carboxylfluorescein and intracellular pH (pHi) measured spectrofluorometrically. Monolayers were studied at ambient temperature on days 3-4 in culture, coincident with the development of high tissue resistance (RT > or = 2000 omega.cm2). Cells were incubated in HCO(3-)-free Na+ buffer [(in mM) 140 NaCl, 6 HEPES, pH 7.4] and acidified by NH3 prepulse. Rates of realkalinization (JH+) were calculated as the product of the initial rate of recovery (dpHi/dt) and the intracellular buffer capacity (beta i). Under control conditions, recovery occurred with an initial JH+ of 28.4 mM/min. When 100 microM dimethylamiloride (DMA), an amiloride analogue with enhanced specificity for inhibiting the Na(+)-H+ antiporter, was present in the basolateral fluid, recovery was inhibited by > 90%. Conversely, when the monolayers were acidified in Na+ buffer containing DMA (100 microM) in the apical fluid, acidification and recovery were identical to control. Recovery from acidification was inhibited by basolateral DMA with a one-half maximal inhibitory concentration (IC50) of 100 nm and by basolateral amiloride with an IC50 of 10 microns. Recovery was completely inhibited by omission of Na+ from the basolateral fluid, but omission of Na+ from apical fluid had no effect. We conclude that Na(+)-H+ antiport activity is located exclusively on the basolateral surface of these alveolar epithelial cell monolayers, where it most likely represents the high-amiloride affinity isoform of the Na(+)-H+ antiporter, NHE-1. The Na(+)-H+ antiporter, asymmetrically distributed to the basolateral surface of the polarized alveolar epithelium, contributes to intracellular homeostasis in alveolar pneumocytes and may also play a role in signal transduction in these cells.

摘要

在本研究中,我们调查了肺泡上皮细胞单层中Na(+)-H+逆向转运活性的极化分布。将大鼠II型肺泡上皮细胞培养在可拆卸的经组织培养处理的核孔滤膜上。将带有完整肺泡上皮细胞单层的膜滤器安装在一个小室中,该小室设计为包含由单层分隔的两个液室。用pH敏感染料2',7'-双羧乙基-5,6-羧基荧光素加载细胞,并通过荧光分光光度法测量细胞内pH(pHi)。在培养的第3 - 4天,于环境温度下研究单层细胞,此时组织电阻较高(RT≥2000Ω·cm2)。将细胞置于不含HCO(3-)的Na+缓冲液[(以mM计)140 NaCl, 6 HEPES, pH 7.4]中,并用NH3预脉冲酸化。再碱化速率(JH+)计算为初始恢复速率(dpHi/dt)与细胞内缓冲能力(βi)的乘积。在对照条件下,初始JH+为28.4 mM/min时发生恢复。当基底外侧液中存在100μM二甲基氨氯吡脒(DMA),一种对抑制Na(+)-H+逆向转运体具有增强特异性的氨氯吡脒类似物时,恢复受到>90%的抑制。相反,当单层细胞在顶端液中含有DMA(100μM)的Na+缓冲液中酸化时,酸化和恢复与对照相同。基底外侧DMA对酸化恢复的抑制作用,其半数最大抑制浓度(IC50)为100 nM,基底外侧氨氯吡脒的IC50为10μM。从基底外侧液中去除Na+可完全抑制恢复,但从顶端液中去除Na+则无影响。我们得出结论,Na(+)-H+逆向转运活性仅位于这些肺泡上皮细胞单层的基底外侧表面,在那里它很可能代表Na(+)-H+逆向转运体的高氨氯吡脒亲和力异构体NHE-1。Na(+)-H+逆向转运体不对称地分布于极化肺泡上皮的基底外侧表面,有助于肺泡上皮细胞内的稳态,也可能在这些细胞的信号转导中起作用。

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