Differential activation of system A and betaine/GABA transport in MDCK cell membranes by hypertonic stress

被引:32
作者
Kempson, SA [1 ]
机构
[1] Indiana Univ, Sch Med, Dept Physiol & Biophys, Indianapolis, IN 46202 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES | 1998年 / 1372卷 / 01期
关键词
alpha-(methylamino)isobutyric acid; gamma-aminobutyric acid; membrane transport; osmotic stress; actinomycin D; cycloheximide;
D O I
10.1016/S0005-2736(98)00051-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Accumulation of osmolytes by renal cells is due in part to increased uptake via specific transporters. These include amino acid transport system A and the betaine/GABA transporter (BGT1). Transport changes have been characterized using intact cells which makes the intracellular mechanisms difficult to determine. In this study the hypertonic upregulation of system A and BGT1 was studied directly at the membrane level in Madin-Darby canine kidney (MDCK) cells. Both system A and BGT1 transport systems were detected in an isolated membrane fraction containing plasma membranes. System A transport was increased in membranes prepared from cells after 6 h hypertonic stress (449 mosmol/kg) but BGT1 activity was minimal and not different from isotonic controls. The increase in system A was blocked by inhibitors of RNA and protein synthesis. BGT1 transport was induced in membranes prepared after 24 h hypertonicity. At this time system A activity in the membrane fraction remained increased, unlike the downregulation observed in intact MDCK cells. We conclude that differential upregulation of system A and BGT1 by hypertonic stress is due to intrinsic changes in these transporters at the membrane level. In contrast, the downregulation of system A in intact cells when hypertonicity is prolonged for 24 h is Likely due to the action of an intracellular repressor that is not present in the isolated membranes. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:117 / 123
页数:7
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