Durante W, Liao L, Iftikhar I, Cheng K, Schafer A I
Houston Veterans Affairs Medical Center, Texas 77030, USA.
J Biol Chem. 1996 May 17;271(20):11838-43. doi: 10.1074/jbc.271.20.11838.
Since recent studies demonstrated that platelet-derived growth factor (PDGF) induces vascular smooth muscle cell (SMC) proliferation by stimulating polyamine synthesis, we examined whether the transcellular transport of L-ornithine, the cationic amino acid precursor of polyamines, could regulate the mitogenic response of PDGF. Treatment of SMC with PDGF stimulated DNA and putrescine synthesis, and this was enhanced further by increasing the extracellular concentration of L-ornithine. The potentiating effect of L-ornithine was reversed by the competitive inhibitor of cationic amino acid transport, methyl-L-arginine, or by preventing putrescine formation with alpha-difluoromethylornithine. Cationic amino acid uptake by SMC was Na+-independent and was mediated by both a high and low affinity carrier system. Treatment of SMC with PDGF initially (0-2 h) decreased basic amino acid transport, while longer exposures (6-24 h) progressively increased uptake. Kinetic studies indicated that PDGF-induced inhibition was associated with a decrease in affinity for cationic amino acids, while the stimulation was mediated by an increase in transport capacity. Endogenous PDGF released by collagen-activated platelets likewise up-regulated cationic amino acid transport in SMC. Reverse transcriptase-polymerase chain reaction detected the presence of mRNA encoding two distinct cationic amino acid transporter (CAT) proteins, CAT-1 and CAT-2B. Treatment of SMC with PDGF strongly induced the expression CAT-2B mRNA and modestly elevated the level of CAT-1 mRNA. These results demonstrate that PDGF-induced polyamine synthesis and SMC mitogenesis are dependent on the transcellular transport of L-ornithine. The capacity of PDGF to up-regulate the transport of L-ornithine by inducing the expression of the genes for CAT-1 and CAT-2B may modulate its mitogenic effect by providing SMC with the necessary intracellular precursor for polyamine biosynthesis.
由于最近的研究表明血小板衍生生长因子(PDGF)通过刺激多胺合成来诱导血管平滑肌细胞(SMC)增殖,我们研究了多胺的阳离子氨基酸前体L-鸟氨酸的跨细胞转运是否能够调节PDGF的促有丝分裂反应。用PDGF处理SMC可刺激DNA和腐胺合成,并且通过增加细胞外L-鸟氨酸浓度可进一步增强这种作用。L-鸟氨酸的增强作用可被阳离子氨基酸转运的竞争性抑制剂甲基-L-精氨酸逆转,或者通过用α-二氟甲基鸟氨酸阻止腐胺形成来逆转。SMC对阳离子氨基酸的摄取不依赖于Na +,并且由高亲和力和低亲和力载体系统介导。用PDGF处理SMC最初(0 - 2小时)会降低碱性氨基酸转运,而较长时间暴露(6 - 24小时)会逐渐增加摄取。动力学研究表明,PDGF诱导的抑制与对阳离子氨基酸的亲和力降低有关,而刺激是由转运能力增加介导的。胶原激活的血小板释放的内源性PDGF同样上调了SMC中阳离子氨基酸的转运。逆转录酶 - 聚合酶链反应检测到编码两种不同阳离子氨基酸转运蛋白(CAT),即CAT-1和CAT-2B的mRNA的存在。用PDGF处理SMC强烈诱导CAT-2B mRNA的表达,并适度提高CAT-1 mRNA的水平。这些结果表明,PDGF诱导的多胺合成和SMC有丝分裂依赖于L-鸟氨酸的跨细胞转运。PDGF通过诱导CAT-1和CAT-2B基因的表达来上调L-鸟氨酸转运的能力,可能通过为SMC提供多胺生物合成所需的细胞内前体来调节其促有丝分裂作用。