CAT2-mediated L-arginine transport and nitric oxide production in activated macrophages

被引:93
作者
Kakuda, DK
Sweet, MJ
MacLeod, CL
Hume, DA
Markovich, D [1 ]
机构
[1] Univ Queensland, Dept Physiol & Pharmacol, Brisbane, Qld 4072, Australia
[2] Univ Queensland, Dept Microbiol, Brisbane, Qld 4072, Australia
[3] Univ Queensland, Dept Biochem, Brisbane, Qld 4072, Australia
[4] Univ Queensland, Ctr Cellular & Mol Biol, Brisbane, Qld 4072, Australia
[5] Univ Calif San Diego, Dept Med, La Jolla, CA 92093 USA
[6] Univ Calif San Diego, Canc Genet Program, La Jolla, CA 92093 USA
关键词
amino acid; antisense inhibition; iNOS; NO; Xenopus oocyte;
D O I
10.1042/0264-6021:3400549
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
Activated macrophages require L-arginine uptake to sustain NO synthesis. Several transport systems could mediate this L-arginine influx. Using competition analysis and gene-expression studies, amino acid transport system yt was identified as the major carrier responsible for this activity. To identify which of the four known y(+) transport-system genes is involved in macrophage-induced L-arginine uptake, we used a hybrid-depletion study in Xenopus oocytes. Cationic amino acid transporter (CAT) 2 antisense oligodeoxyribonucleotides abolished the activated-macrophage-mRNA-induced L-arginine transport. Together with expression studies documenting that CAT2 mRNA and protein levels are elevated with increased L-arginine uptake, our data demonstrate that CAT2 mediates the L-arginine transport that is required for the raised NO production in activated J774 macrophages.
引用
收藏
页码:549 / 553
页数:5
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