Maeda Tomoji, Shima Yoichiro, Sugiura Shigeki, Aizawa Shin, Tamai Ikumi
Department of Membrane Transport and Pharmacokinetics, Faculty of Pharmaceutical Sciences, Tokyo University of Science, Chiba, Japan.
Drug Metab Pharmacokinet. 2008;23(3):181-7. doi: 10.2133/dmpk.23.181.
We recently showed that arginine transport via cationic amino acid transporter 1 (CAT1), which transports arginine, lysine, ornithine, and histidine, is essential for erythropoiesis. In the present study, to confirm the importance of both arginine and CAT1 in erythropoiesis, we investigated the relationship of arginine uptake activity and differentiation and proliferation of blood cells by knockdown of the CAT1 gene using shRNA. Five short hairpin RNA (shRNA)-transfected K562 cell clones, in which the CAT1 mRNA expression level is decreased, and a vector-transfected clone were obtained. The differentiation to erythrocytes and proliferation of K562 cells were decreased by knockdown of CAT1. In addition, the initial uptake rate of [(3)H]arginine was decreased in the shRNA-transfected cell clones. The ratio of differentiation of CAT1-knockdown K562 cells was well correlated with the uptake activity for arginine by the cells (R(2)=0.59). These findings indicate that CAT1 is directly involved in erythropoiesis through supplying arginine to the blood cells.
我们最近发现,通过阳离子氨基酸转运体1(CAT1)转运精氨酸、赖氨酸、鸟氨酸和组氨酸,对红细胞生成至关重要。在本研究中,为了证实精氨酸和CAT1在红细胞生成中的重要性,我们使用短发夹RNA(shRNA)敲低CAT1基因,研究了精氨酸摄取活性与血细胞分化和增殖之间的关系。获得了五个转染短发夹RNA(shRNA)的K562细胞克隆,其中CAT1 mRNA表达水平降低,以及一个转染载体的克隆。敲低CAT1可降低K562细胞向红细胞的分化和增殖。此外,转染shRNA的细胞克隆中[³H]精氨酸的初始摄取率降低。CAT1敲低的K562细胞的分化率与细胞对精氨酸的摄取活性密切相关(R² = 0.59)。这些发现表明,CAT1通过向血细胞供应精氨酸直接参与红细胞生成。