Padh H, Aleo J J
Biochim Biophys Acta. 1987 Jul 23;901(2):283-90. doi: 10.1016/0005-2736(87)90125-8.
Ascorbic acid transport by 3T6 mouse skin fibroblasts has been characterized using radiometric technique with L-[1-14C]ascorbic acid under the conditions in which oxidation of ascorbic acid was prevented by addition of 1 mM thiourea. The ascorbate transport is temperature-dependent with the energy of activation E and Q10 of 13.3 kcal/mol and 2.0, respectively. The transport requires energy and exhibits Michaelis-Menten kinetics with an apparent Km of 112 microM and Vmax of 158 pmol/min per mg protein, when the extracellular Na+ concentration is 150 mM. The ascorbate transport requires presence of extracellular Na+ and can be inhibited by ouabain treatment. At 40 and 200 microM ascorbate concentrations, respectively, 1.4 and 1.0 moles of Na+ bound the transporter molecule per each mole of ascorbate transported. Increased Na+ binding to the transporter at lower ascorbate concentration may signify multiple Na+-binding sites or ascorbate concentration dependent conformational changes in the transporter molecule. Increasing Na+ concentration decreases Km without affecting Vmax, suggesting that Na+ increases affinity of ascorbate for the transporter molecule without affecting translocation process. An increase in ascorbate concentration reduces the number of Na+ bound to the transporter from 1.4 to 1.0. The ascorbate transport is stimulated by Ca2+ and other divalent cations. The mechanism of stimulation by Ca2+ is not clear. Calcium increases both the Km and Vmax. The data presented support the hypothesis that the ascorbate transport by 3T6 fibroblasts is an energy and temperature-dependent active process driven by the Na+ electrochemical gradient. A potent inhibitor of ascorbate transport is also demonstrated in human serum.
利用放射性技术,在添加1 mM硫脲以防止抗坏血酸氧化的条件下,用L-[1-14C]抗坏血酸对3T6小鼠皮肤成纤维细胞的抗坏血酸转运进行了表征。抗坏血酸盐转运具有温度依赖性,活化能E和Q10分别为13.3 kcal/mol和2.0。当细胞外Na+浓度为150 mM时,转运需要能量,并呈现米氏动力学,表观Km为112 microM,Vmax为每毫克蛋白质158 pmol/min。抗坏血酸盐转运需要细胞外Na+的存在,并且可以被哇巴因处理所抑制。在抗坏血酸盐浓度分别为40和200 microM时,每转运1摩尔抗坏血酸盐,有1.4和1.0摩尔的Na+与转运蛋白分子结合。在较低抗坏血酸盐浓度下,Na+与转运蛋白的结合增加,这可能意味着转运蛋白分子中有多个Na+结合位点或抗坏血酸盐浓度依赖性的构象变化。增加Na+浓度会降低Km而不影响Vmax,表明Na+增加了抗坏血酸对转运蛋白分子的亲和力而不影响转运过程。抗坏血酸盐浓度的增加会使与转运蛋白结合的Na+数量从1.4减少到1.0。抗坏血酸盐转运受到Ca2+和其他二价阳离子的刺激。Ca2+的刺激机制尚不清楚。钙会增加Km和Vmax。所提供的数据支持以下假设:3T6成纤维细胞的抗坏血酸盐转运是一个由Na+电化学梯度驱动的能量和温度依赖性的主动过程。在人血清中也证实了一种有效的抗坏血酸盐转运抑制剂。