Yuasa S, Hamprecht B
J Neurochem. 1987 Aug;49(2):528-35. doi: 10.1111/j.1471-4159.1987.tb02896.x.
The transport of taurine into membrane vesicles prepared from neuroblastoma x glioma hybrid cells 108CC5 was studied. A great part of the taurine uptake by the membrane preparation is due to the transport into an osmotically sensitive space of membrane vesicles. Taurine uptake by membrane vesicles is an active transport driven by the concentration gradient of Na+ across the membrane (outside concentration greater than inside). The Km value of 36 microM for Na+-dependent taurine uptake indicates a high-affinity transport system. The rate of taurine transport by the membrane vesicles is enhanced by the K+ gradient (inside concentration greater than outside) and the K+ ionophore valinomycin. Taurine transport is inhibited by several structural analogs of taurine: hypotaurine, beta-alanine, and taurocyamine. All these results indicate that the taurine transport system of the membrane vesicles displays properties almost identical to those of intact neuroblastoma X glioma hybrid cells.
对从神经母细胞瘤x胶质瘤杂交细胞108CC5制备的膜囊泡中牛磺酸的转运进行了研究。膜制剂对牛磺酸的摄取很大一部分是由于其转运到膜囊泡的渗透敏感空间。膜囊泡对牛磺酸的摄取是一种由Na+跨膜浓度梯度驱动的主动转运(外部浓度大于内部)。Na+依赖性牛磺酸摄取的Km值为36 microM,表明存在高亲和力转运系统。膜囊泡对牛磺酸的转运速率因K+梯度(内部浓度大于外部)和K+离子载体缬氨霉素而增强。牛磺酸转运受到牛磺酸的几种结构类似物的抑制:亚牛磺酸、β-丙氨酸和氨基乙磺酸。所有这些结果表明,膜囊泡的牛磺酸转运系统表现出与完整神经母细胞瘤x胶质瘤杂交细胞几乎相同的特性。