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具有近端肾小管细胞特征的上皮细胞系(LLC-PK1)中的钠离子传导运输

Conductive Na+ transport in an epithelial cell line (LLC-PK1) with characteristics of proximal tubular cells.

作者信息

Cantiello H F, Scott J A, Rabito C A

出版信息

Am J Physiol. 1987 Apr;252(4 Pt 2):F590-7. doi: 10.1152/ajprenal.1987.252.4.F590.

DOI:10.1152/ajprenal.1987.252.4.F590
PMID:3031998
Abstract

Na+ influx and efflux from confluent monolayers of an epithelial cell line with multiple differentiated characteristics of the straight segment of the renal proximal tubule were studied in the presence and absence of a pH gradient. The results show that Na+ influx in the absence of a pH gradient is inhibited by amiloride as well as by complete replacement of Cl- by an impermeable anion, such as isethionate. Dissipation of cell membrane potential by increasing the potassium concentration of the extracellular medium in the presence of valinomycin also inhibited Na+ influx, whereas sodium influx induced by an H+ gradient was not affected. Inhibition of Na+ influx by different maneuvers produced hyperpolarization of the plasma cell membrane, as would be expected if the sodium movement involved net displacement of charges. Calcium and other divalent and trivalent cations also inhibited Na+ influx measured in the absence of an H+ gradient. Na+ influx induced by a pH gradient, however, was not affected. Like the Na+-H+-exchange system, the conductive Na+ pathway is localized in the apical membrane of the epithelial cells. From these results, we conclude that at least a fraction of transepithelial Na+ transport in LLC-PK1 monolayers occurs through a simple rheogenic transport system.

摘要

在有和没有pH梯度的情况下,研究了具有肾近端小管直段多种分化特征的上皮细胞系汇合单层中Na⁺的流入和流出。结果表明,在没有pH梯度的情况下,氨氯吡咪以及用不可渗透的阴离子(如羟乙磺酸盐)完全替代Cl⁻可抑制Na⁺流入。在缬氨霉素存在下,通过增加细胞外培养基中的钾浓度来消散细胞膜电位也抑制了Na⁺流入,而由H⁺梯度诱导的钠流入则不受影响。通过不同操作抑制Na⁺流入会导致质膜超极化,这正如如果钠的移动涉及净电荷位移所预期的那样。钙以及其他二价和三价阳离子也抑制了在没有H⁺梯度时测量的Na⁺流入。然而,由pH梯度诱导的Na⁺流入不受影响。与Na⁺-H⁺交换系统一样,传导性Na⁺途径定位于上皮细胞的顶端膜。从这些结果中,我们得出结论,LLC-PK1单层中的跨上皮Na⁺转运至少有一部分是通过简单的生电转运系统进行的。

相似文献

1
Conductive Na+ transport in an epithelial cell line (LLC-PK1) with characteristics of proximal tubular cells.具有近端肾小管细胞特征的上皮细胞系(LLC-PK1)中的钠离子传导运输
Am J Physiol. 1987 Apr;252(4 Pt 2):F590-7. doi: 10.1152/ajprenal.1987.252.4.F590.
2
Polarized distribution of the Na+/H+ exchange system in a renal cell line (LLC-PK1) with characteristics of proximal tubular cells.具有近端肾小管细胞特征的肾细胞系(LLC-PK1)中Na+/H+交换系统的极化分布。
J Biol Chem. 1986 Mar 5;261(7):3252-8.
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Sodium-hydrogen exchange system in LLC-PK1 epithelium.LLC-PK1上皮细胞中的钠氢交换系统。
Am J Physiol. 1987 Jan;252(1 Pt 1):C63-7. doi: 10.1152/ajpcell.1987.252.1.C63.
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Coupling of Na-H exchange and Na-K pump activity in cultured rat proximal tubule cells.培养的大鼠近端小管细胞中钠氢交换与钠钾泵活性的偶联
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Pharmacologically different Na/H antiporters on the apical and basolateral surfaces of cultured porcine kidney cells (LLC-PK1).培养的猪肾细胞(LLC-PK1)顶膜和基底外侧膜上药理学特性不同的钠/氢交换体
Proc Natl Acad Sci U S A. 1988 Sep;85(18):6797-801. doi: 10.1073/pnas.85.18.6797.
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Increased Na(+)-H+ antiporter activity in apical membrane vesicles from mutant LLC-PK1 cells.突变型LLC-PK1细胞顶端膜囊泡中钠氢交换体活性增加。
Am J Physiol. 1991 Apr;260(4 Pt 1):C738-44. doi: 10.1152/ajpcell.1991.260.4.C738.
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Sodium cotransport processes in renal epithelial cell lines.肾上皮细胞系中的钠协同转运过程。
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Cystine dimethyl ester reduces the forces driving sodium-dependent transport in LLC-PK1 cells.胱氨酸二甲酯降低了LLC-PK1细胞中驱动钠依赖性转运的驱动力。
Am J Physiol. 1992 Aug;263(2 Pt 1):C516-20. doi: 10.1152/ajpcell.1992.263.2.C516.

引用本文的文献

1
Effects of cell differentiation on ion conductances and membrane voltage in LLC-PK1 cells.细胞分化对LLC-PK1细胞离子电导和膜电压的影响。
Pflugers Arch. 1995 Jan;429(3):370-7. doi: 10.1007/BF00374152.
2
Membrane localization of the pertussis toxin-sensitive G-protein subunits alpha i-2 and alpha i-3 and expression of a metallothionein-alpha i-2 fusion gene in LLC-PK1 cells.百日咳毒素敏感的G蛋白亚基αi - 2和αi - 3的膜定位以及金属硫蛋白-αi - 2融合基因在LLC - PK1细胞中的表达。
Proc Natl Acad Sci U S A. 1990 Jun;87(12):4635-9. doi: 10.1073/pnas.87.12.4635.
3
Millimolar amiloride concentrations block K conductance in proximal tubular cells.
毫摩尔浓度的氨氯吡咪可阻断近端肾小管细胞的钾离子电导。
Br J Pharmacol. 1992 Oct;107(2):532-8. doi: 10.1111/j.1476-5381.1992.tb12779.x.