Sips H J, van Dam K
J Membr Biol. 1981;62(3):231-7. doi: 10.1007/BF01998168.
The L-alanine-dependent transport of sodium ions across the plasma membrane of rat-liver parenchymal cells was studied using isolated plasma membrane vesicles. Sodium uptake is stimulated specifically by the L-isomer of alanine and other amino acids, whose transport is sodium-dependent in rat-liver plasma membrane vesicles. The L-alanine-dependent sodium flux across the membrane is inhibited by an excess of Li+ ions, but not by K+ or choline ions. Sodium transport is sensitive to -SH reagents and ionophores, and is an electrogenic process: a membrane potential (negative inside) can enhance L-alanine-dependent sodium accumulation. The data presented provide further evidence for a sodium-alanine cotransport mechanism.
利用分离的质膜囊泡,研究了L-丙氨酸依赖的钠离子跨大鼠肝脏实质细胞质膜的转运。丙氨酸的L-异构体和其他氨基酸可特异性刺激钠摄取,其转运在大鼠肝脏质膜囊泡中依赖于钠。过量的Li+离子可抑制跨膜的L-丙氨酸依赖的钠通量,但K+或胆碱离子则无此作用。钠转运对-SH试剂和离子载体敏感,是一个生电过程:膜电位(内侧为负)可增强L-丙氨酸依赖的钠积累。所提供的数据为钠-丙氨酸共转运机制提供了进一步的证据。