Involvement of transporter recruitment as well as gene expression in the substrate-induced adaptive regulation of amino acid transport system A

被引:87
作者
Ling, R
Bridges, CC
Sugawara, M
Fujita, T
Leibach, FH
Prasad, PD
Ganapathy, V [1 ]
机构
[1] Med Coll Georgia, Dept Biochem & Mol Biol, Augusta, GA 30912 USA
[2] Kyoto Pharmaceut Univ, Dept Biopharmaceut & Biochem Pharmacol, Kyoto 6078414, Japan
[3] Med Coll Georgia, Dept Obstet & Gynecol, Augusta, GA 30912 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES | 2001年 / 1512卷 / 01期
关键词
system A; adaptive regulation; amino acid starvation; transporter recruitment; gene expression; glioma cell;
D O I
10.1016/S0005-2736(01)00310-8
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
We investigated the molecular mechanism involved in the adaptive regulation of the amino acid transport system Al a process in which amino acid starvation induces the transport activity. These studies were done with rat C6 glioma cells. System A activity in these cells is mediated exclusively by the system A subtype, amino acid transporter A2 (ATA2). The other two known system A subtypes, ATA1 and ATA3, are not expressed in these cells. Exposure of these cells to an amino acid-free medium induces system A activity. This process consists of an acute phase and a chronic phase. Laser-scanning confocal microscopic immunolocalization of ATA2 reveals that the acute phase is associated with recruitment of preformed ATA2 from an intracellular pool to the plasma membrane. In contrast, the chronic phase is associated with an induction of nta gene expression as evidenced from the increase in the steady-state levels of ATA2 mRNA, restoration of the intracellular pool of ATA2 protein, and blockade of the induction by cycloheximide and actinomycin D. The increase in system A activity induced by amino acid starvation is blocked specifically by system A substrates, including the non-metabolizable alpha-(methylamino)isobutyric acid. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:15 / 21
页数:7
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