Yamamoto Toshifumi, Nishizaki Itone, Nukada Toshihide, Kamegaya Etsuko, Furuya Shigeki, Hirabayashi Yoshio, Ikeda Kazutaka, Hata Harumi, Kobayashi Hideaki, Sora Ichiro, Yamamoto Hideko
Laboratory of Molecular Recognition, Graduate School of Integrated Science, Yokohama City University, 22-2 Seto, Kanazawa-ku, Yokohama 236-0027, Japan.
Neurosci Res. 2004 May;49(1):101-11. doi: 10.1016/j.neures.2004.02.004.
The uptake of L-serine, a nonessential amino acid known to be transported by the neutral amino acid transporter system ASC, was studied in primary cultures of rat neurons and astrocytes, and compared with that in human embryonic kidney (HEK293) cells transfected with rat ASCT1 cDNA. We first cloned neutral amino acid transporter ASCT1 from rat neurons in primary culture as a transporter candidate for L-serine uptake in the brain. The predicted amino acid sequence from rat ASCT1 exhibited significant homology with mouse and human ASCT1s. The amino acid sequence of rat ASCT1 was 92 and 84% identical to that of mouse and of human ASCT1, respectively. HEK293 cells expressing the rat ASCT1 cDNA showed a saturable dose-dependent and Na(+)-dependent increase in L-[(3)H] serine uptake by high affinity ( K(m) = 67 microM). The substrate selectivity of rat ASCT1 was the same as those of the mouse and human transporter. Northern blot analysis revealed that ASCT1 mRNA was ubiquitously expressed in the brain, with its highest concentration in the striatum and hippocampus. When the uptake of L -[(3)H] serine into rat primary neurons or astrocytes was compared with that of HEK293 cells expressing rat ASCT1 or rat ASCT2 cDNA, the inhibition profile of amino acids for the rat neurons quite resembled that for HEK293 cells expressing rat ASCT1. In contrast, the profile for rat astrocytes was a mixture of that for HEK293 cells expressing rat ASCT1 and that for the cells expressing rat ASCT2. Furthermore, L-[(3)H] serine uptake in neurons was fully Na(+)-dependent. ASCT1 mRNA was expressed in both primary neurons and astrocytes, whereas ASCT2 mRNA was expressed only in astrocytes, as determined by using RT-PCR with primers specific for the rat ASCT1 or rat ASCT2 transporter. Taken together, these findings indicate that ASCT1 predominantly contributes to the uptake of L-serine in primary neurons.
L-丝氨酸是一种已知由中性氨基酸转运体系统ASC转运的非必需氨基酸,本研究在大鼠神经元和星形胶质细胞的原代培养物中对其摄取情况进行了研究,并与转染了大鼠ASCT1 cDNA的人胚肾(HEK293)细胞中的摄取情况进行了比较。我们首先从原代培养的大鼠神经元中克隆了中性氨基酸转运体ASCT1,作为大脑中L-丝氨酸摄取的转运体候选物。大鼠ASCT1预测的氨基酸序列与小鼠和人ASCT1具有显著同源性。大鼠ASCT1的氨基酸序列与小鼠和人ASCT1的氨基酸序列分别有92%和84%的同一性。表达大鼠ASCT1 cDNA的HEK293细胞通过高亲和力(K(m)=67 microM)表现出L-[(3)H]丝氨酸摄取的饱和剂量依赖性和Na(+)依赖性增加。大鼠ASCT1的底物选择性与小鼠和人转运体相同。Northern印迹分析显示,ASCT1 mRNA在大脑中普遍表达,在纹状体和海马体中浓度最高。当将L -[(3)H]丝氨酸进入大鼠原代神经元或星形胶质细胞的摄取与表达大鼠ASCT1或大鼠ASCT2 cDNA的HEK293细胞的摄取进行比较时,氨基酸对大鼠神经元的抑制谱与表达大鼠ASCT1的HEK293细胞的抑制谱非常相似。相反,大鼠星形胶质细胞的谱是表达大鼠ASCT1的HEK293细胞和表达大鼠ASCT2的细胞的谱的混合。此外,神经元中L-[(3)H]丝氨酸的摄取完全依赖于Na(+)。通过使用针对大鼠ASCT1或大鼠ASCT2转运体的特异性引物进行RT-PCR测定,发现ASCT1 mRNA在原代神经元和星形胶质细胞中均有表达,而ASCT2 mRNA仅在星形胶质细胞中表达。综上所述,这些发现表明ASCT1在原代神经元中主要负责L-丝氨酸的摄取。