Béliveau R, Ibnoul-Khatib H
Département de Chimie, Université du Québec à Montréal, Canada.
Biochem J. 1988 Jun 15;252(3):801-6. doi: 10.1042/bj2520801.
Phosphate uptake by rat renal brush-border membrane vesicles was studied under experimental conditions where transmembrane electrical potential (delta psi) could be manipulated. Experiments were performed under initial rate conditions to avoid complications associated with the dissipation of ion gradients. First, phosphate uptake was shown to be strongly affected by the nature of Na+ co-anions, the highest rates of uptake being observed with 100 mM-NaSCN (1.010 +/- 0.086 pmol/5 s per micrograms of protein) and the lowest with 50 mM-Na2SO4 (0.331 +/- 0.046 pmol/5 s per micrograms of protein). Anion substitution studies showed that potency of the effect of the co-anions was in the order thiocyanate greater than nitrate greater than chloride greater than isethionate greater than gluconate greater than sulphate, which correlates with the known permeability of the membrane to these anions and thus to the generation of transmembrane electrical potentials of decreasing magnitude (inside negative). The stimulation by ion-diffusion-induced potential was observed from pH 6.5 to 8.5, indicating that the transport of both monovalent and divalent phosphate was affected. In addition, inside-negative membrane potentials were generated by valinomycin-induced diffusion of K+ from K+-loaded vesicles and showed a 57% stimulation of phosphate uptake, at pH 7.5. Similar experiments with H+-loaded vesicles, in the presence of carbonyl cyanide m-chlorophenylhydrazone gave a 50% stimulation compared with controls. Inside-positive membrane potentials were also induced by reversal of the K+ gradient (outside greater than inside) in the presence of valinomycin and gave 58% inhibition of phosphate uptake. The membrane-potential dependency of phosphate uptake was finally analysed under thermodynamic equilibrium, and a stimulation by inside-negative potential was observed. The transport of phosphate was thus driven against a concentration gradient by a membrane potential, implicating the net transfer of a positive charge during the translocation process. These results indicate a major contribution of electrical potential to phosphate uptake in renal brush-border membranes.
在可操控跨膜电势(Δψ)的实验条件下,研究了大鼠肾刷状缘膜囊泡对磷酸盐的摄取。实验在初始速率条件下进行,以避免与离子梯度耗散相关的并发症。首先,磷酸盐摄取受Na⁺共阴离子性质的强烈影响,在100 mM - NaSCN时观察到最高摄取速率(每微克蛋白质1.010±0.086 pmol/5 s),在50 mM - Na₂SO₄时最低(每微克蛋白质0.331±0.046 pmol/5 s)。阴离子替代研究表明,共阴离子效应的效力顺序为硫氰酸盐>硝酸盐>氯化物>羟乙磺酸盐>葡萄糖酸盐>硫酸盐,这与膜对这些阴离子的已知通透性相关,进而与跨膜电势大小递减(内侧为负)的产生相关。在pH 6.5至8.5范围内观察到离子扩散诱导电势的刺激作用,表明单价和二价磷酸盐的转运均受到影响。此外,缬氨霉素诱导K⁺从负载K⁺的囊泡中扩散产生内侧为负的膜电势,在pH 7.5时显示磷酸盐摄取增加57%。在羰基氰化物间氯苯腙存在下,对负载H⁺的囊泡进行类似实验,与对照相比摄取增加50%。在缬氨霉素存在下,通过逆转K⁺梯度(外侧>内侧)也可诱导内侧为正的膜电势,并导致磷酸盐摄取抑制58%。最后在热力学平衡条件下分析了磷酸盐摄取对膜电势的依赖性,观察到内侧为负的电势具有刺激作用。因此,磷酸盐的转运是由膜电势逆浓度梯度驱动的,这意味着在转运过程中有正电荷的净转移。这些结果表明电势对肾刷状缘膜中磷酸盐摄取有重要贡献。