Furman S, Lichtstein D, Ilani A
Department of Physiology, The Hebrew University-Hadassah Medical School, Jerusalem, Israel.
Biochim Biophys Acta. 1997 Apr 3;1325(1):34-40. doi: 10.1016/s0005-2736(96)00238-6.
Sodium-dependent phosphate entry into neuronal cells was demonstrated in synaptic plasma membrane vesicles and synaptosomes prepared from rat brains, in PC12 cells and in primary culture of pituitary cells. The extent of the sodium-dependent phosphate transport in the synaptic plasma membrane preparation, at [Na]out = 110 mM and [P(i)]out = 0.1 mM, varied between 0.28 to 1.02 nmol phosphate/mg membrane protein/min. In pituitary cells the value was only about 0.05 nmol P(i)/mg protein/min. In PC12 cells the activity increased from 0.0085 to 0.26 nmol P(i)/mg protein/min in the transit from undifferentiated to differentiated cells. The dependence of phosphate on sodium concentrations fits a model in which two sodium ions are required to transfer the phosphate into the cells with a K[Na]0.5 of 43 mM. The K(m) for the phosphate transport in the synaptic plasma membrane preparations was between 0.1 and 0.45 mM. It is concluded that sodium-driven active transport of phosphate is a ubiquitous activity in various types of neuronal cells.
在从大鼠脑制备的突触质膜囊泡和突触体、PC12细胞以及垂体细胞原代培养物中,均证实了钠依赖性磷酸盐进入神经元细胞的过程。在突触质膜制剂中,当细胞外[Na] = 110 mM且细胞外[P(i)] = 0.1 mM时,钠依赖性磷酸盐转运的程度在0.28至1.02 nmol磷酸盐/毫克膜蛋白/分钟之间变化。在垂体细胞中,该值仅约为0.05 nmol P(i)/毫克蛋白/分钟。在PC12细胞中,从未分化细胞转变为分化细胞的过程中,活性从0.0085增加至0.26 nmol P(i)/毫克蛋白/分钟。磷酸盐对钠浓度的依赖性符合一个模型,即需要两个钠离子将磷酸盐转运到细胞中,其半最大激活浓度(K[Na]0.5)为43 mM。突触质膜制剂中磷酸盐转运的米氏常数(K(m))在0.1至0.45 mM之间。得出的结论是,钠驱动的磷酸盐主动转运在各种类型的神经元细胞中是一种普遍存在的活动。