Bergsten P, Yu R, Kehrl J, Levine M
Laboratory of Cell Biology and Genetics, National Institute of Diabetes, Digestive, and Kidney Diseases, National Institutes of Health, Bethesda, Maryland 20892.
Arch Biochem Biophys. 1995 Feb 20;317(1):208-14. doi: 10.1006/abbi.1995.1155.
Ascorbic acid (vitamin C) transport was investigated in human B lymphocytes. The vitamin was transported by two components. The first was a high-affinity activity with an apparent Km of 7-10 microM and Vmax of 0.14 mM/h (3.11 x 10(-4) mumol x h-1 x mg protein-1). The activity was concentration and temperature dependent, saturable, and inhibited by carbonylcyanide-p-trifluoromethoxyphenylhydrazone and ouabain and generated ascorbic acid accumulation against a concentration gradient. Kinetics for the second component were indeterminate because ascorbate was not accumulated against a concentration gradient. Subcellular fractionation revealed that intracellular ascorbic acid in human B lymphocytes was > 90% localized to the cytosol and not protein bound. Kinetic parameters of high-affinity ascorbic acid transport could operate effectively with plasma concentrations normally found in humans.
对人B淋巴细胞中的抗坏血酸(维生素C)转运进行了研究。维生素通过两种成分进行转运。第一种是高亲和力活性,表观Km为7 - 10微摩尔,Vmax为0.14毫摩尔/小时(3.11×10⁻⁴微摩尔·小时⁻¹·毫克蛋白质⁻¹)。该活性与浓度和温度相关,具有饱和性,并受到羰基氰化物 - 对 - 三氟甲氧基苯腙和哇巴因的抑制,且能逆浓度梯度产生抗坏血酸积累。第二种成分的动力学无法确定,因为抗坏血酸盐不能逆浓度梯度积累。亚细胞分级分离显示,人B淋巴细胞中的细胞内抗坏血酸> 90%定位于细胞质溶胶,且不与蛋白质结合。高亲和力抗坏血酸转运的动力学参数在人体正常血浆浓度下可有效发挥作用。