Nicholson B, McGivan J D
Department of Biochemistry, School of Medical Sciences, University of Bristol, United Kingdom.
J Biol Chem. 1996 May 24;271(21):12159-64. doi: 10.1074/jbc.271.21.12159.
In renal epithelial cells amino acid deprivation induces an increase in L-Asp transport with a doubling of the Vmax and no change in Km (4.5 micronM) in a cycloheximide-sensitive process. The induction of sodium-depending L-aspartate transport was inhibited by single amino acids that are metabolized to produce glutamate but not by those that do not produce glutamate. The transaminase inhibitor aminooxyacetate in glutamine-free medium caused a decrease in cell glutamate content and an induction of glutamate transport. In complete medium aminooxyacetate neither decreased cell glutamate nor increased transport activity. These results are consistent with a triggering of induction of transport by low intracellular glutamate concentrations. High affinity glutamate transport in these cells is mediated by the excitatory amino acid carrier 1 (EAAC1) gene product. Western blotting using antibodies to the C-terminal region of EAAC1 showed that there is no increase in the amount of EAAC1 protein on prolonged incubation in amino acid-free medium. Conversely, the induction of high affinity glutamate transport by hyperosmotic shock was accompanied by an increase in EAAC1 protein. It is proposed that low glutamate levels lead to the induction of a putative protein that activates the EAAC1 transporter. A model illustrating such a mechanism is described.
在肾上皮细胞中,氨基酸剥夺会导致L-天冬氨酸转运增加,Vmax加倍,Km(4.5微摩尔)不变,这是一个对放线菌酮敏感的过程。依赖钠的L-天冬氨酸转运的诱导受到代谢生成谷氨酸的单一氨基酸的抑制,但不受不生成谷氨酸的氨基酸的抑制。在无谷氨酰胺培养基中,转氨酶抑制剂氨基氧乙酸导致细胞谷氨酸含量降低,并诱导谷氨酸转运。在完全培养基中,氨基氧乙酸既不降低细胞谷氨酸含量,也不增加转运活性。这些结果与低细胞内谷氨酸浓度触发转运诱导一致。这些细胞中的高亲和力谷氨酸转运由兴奋性氨基酸载体1(EAAC1)基因产物介导。使用针对EAAC1 C末端区域的抗体进行蛋白质印迹分析表明,在无氨基酸培养基中长时间孵育后,EAAC1蛋白量没有增加。相反,高渗休克诱导的高亲和力谷氨酸转运伴随着EAAC1蛋白的增加。有人提出,低谷氨酸水平会导致一种假定蛋白质的诱导,该蛋白质激活EAAC1转运体。描述了一个说明这种机制的模型。