Bowen-Pope D F, Rubin H
Proc Natl Acad Sci U S A. 1977 Apr;74(4):1585-9. doi: 10.1073/pnas.74.4.1585.
Cultures of chick embryo fibroblasts were incubated for varying periods in media containing different concentrations of Ca2+ and Mg2+-Mg2+ deprivation produced a gradual decrease in the Vmax of the glucose transport system for the D-glucose analogues 3-O-[3H]methyl-D-glucose and 2-deoxy-D-[3H]glucose and a parallel decrease in the rate of production of lactate from glucose in the medium. It greatly reduced the rates of [3H]uridine uptake and incorporation by decreasing the Vmax of the uridine transport system. Addition of Mg2+ to Mg2+-deprived cultures rapidly increased the rate of [3H]uridine uptake without requiring protein synthesis and increased the rate of 2-deoxy-D-[3H]glucose uptake without requiring RNA synthesis. These effects of changes in Mg2+ concentration qualitatively reproduce the effects of such variables as cell density and serum and insulin concentrations. Ca2+ deprivation resulted in similar, though much smaller, changes in the activities of the two transport systems, but also greatly increased the "leakiness" of the cells to the nontransported hexose L-[3H]glucose.
将鸡胚成纤维细胞培养物在含有不同浓度Ca2+和Mg2+的培养基中孵育不同时间——去除Mg2+会使葡萄糖转运系统对D-葡萄糖类似物3-O-[3H]甲基-D-葡萄糖和2-脱氧-D-[3H]葡萄糖的Vmax逐渐降低,同时培养基中葡萄糖产生乳酸的速率也平行下降。它通过降低尿苷转运系统的Vmax,极大地降低了[3H]尿苷摄取和掺入的速率。向去除Mg2+的培养物中添加Mg2+会迅速提高[3H]尿苷摄取速率,且无需蛋白质合成,同时提高2-脱氧-D-[3H]葡萄糖摄取速率,且无需RNA合成。Mg2+浓度变化的这些效应定性地重现了细胞密度、血清和胰岛素浓度等变量的效应。去除Ca2+会导致这两种转运系统的活性发生类似但小得多的变化,同时也大大增加了细胞对非转运己糖L-[3H]葡萄糖的“渗漏性”。