Christopher C W, Kohlbacher M S, Amos H
Biochem J. 1976 Aug 15;158(2):439-50. doi: 10.1042/bj1580439.
The rate of D-glucose uptake by cells that had been deprived of sugar for 18-24h was consistently observed to be 15-20 times higher than that in control cells maintained for the same length of time in medium containing glucose. This increased rate of glucose transport by sugar-starved cells was due to a 3-5-fold increase in the Vmax. value of a low-affinity system (Km 1 mM) combined with an increase in the Vmax of a separate high-affinity system (Km 0.05-0.2 mM). The high-affinity system, which was most characteristic of starved cells, was particularly sensitive to low concentrations of the thiol reagent N-ethylmaleimide; 50% inhibition of uptake occurred at approx. 0.01 mM-N-ethylmaleimide. In contrast with the high-affinity system, the low-affinity system of either the fed cells or the starved cells was unaffected by N-ethylmaleimide. In addition to the increases in the rate of D-glucose transport, cells deprived of sugar had increased rates of transport of 3-O-methyl-D-glucose and 2-deoxy-D-glucose. No measurable high-affinity transport system could be demonstrated for the transport of 3-O-methylgucose, and N-ethylmaleimide did not alter the initial rate. Thus the transport of 3-O-methyglucose by both fed and starved cells was exclusively by the N-ethylmaleimide-insensitive low-affinity system. The low-affinity system also appeared to be the primary means for the transport of 2-deoxyglucose by fed and starved cells. However, some of the transport of 2-deoxyglucose by starved cells was inhibited by N-ethylmaleimide, suggesting that 2-deoxyglucose may also be transported by a high-affinity system. The results of experiments that measured transport kinetics strongly suggest that glucose can be transported by a least two separate systems, and 3-O-methylglucose and 2-deoxyglucose by one. Support for these interpretations comes from the analysis of the effects of N-ethylmaleimide and cycloheximide as well as from the results of competition experiments. The uptake of glucose is quite different from that of 2-deoxyglucose and 3-O-methylglucose. The net result of sugar starvation serves to emphasize these differences. The apparent de-repression of the transport systems studied presents an interesting basis for further studies of the regulation of transport in a variety of cells.
在无糖环境中培养18 - 24小时的细胞对D - 葡萄糖的摄取速率,一直被观察到比在含葡萄糖培养基中培养相同时间的对照细胞高15 - 20倍。糖饥饿细胞葡萄糖转运速率的增加,是由于低亲和力系统(Km为1 mM)的Vmax值增加了3 - 5倍,同时一个单独的高亲和力系统(Km为0.05 - 0.2 mM)的Vmax也增加了。高亲和力系统是饥饿细胞最典型的特征,对低浓度的硫醇试剂N - 乙基马来酰胺特别敏感;在约0.01 mM - N - 乙基马来酰胺时,摄取受到50%的抑制。与高亲和力系统不同,饱食细胞或饥饿细胞的低亲和力系统不受N - 乙基马来酰胺的影响。除了D - 葡萄糖转运速率增加外,无糖培养的细胞对3 - O - 甲基 - D - 葡萄糖和2 - 脱氧 - D - 葡萄糖的转运速率也增加。对于3 - O - 甲基葡萄糖的转运,未检测到可测量的高亲和力转运系统,且N - 乙基马来酰胺不改变其初始转运速率。因此,饱食细胞和饥饿细胞对3 - O - 甲基葡萄糖的转运均仅通过对N - 乙基马来酰胺不敏感的低亲和力系统进行。低亲和力系统似乎也是饱食细胞和饥饿细胞转运2 - 脱氧葡萄糖的主要方式。然而,饥饿细胞对2 - 脱氧葡萄糖的部分转运受到N - 乙基马来酰胺的抑制,这表明2 - 脱氧葡萄糖也可能通过高亲和力系统转运。测量转运动力学的实验结果强烈表明,葡萄糖至少可通过两个独立的系统转运,而3 - O - 甲基葡萄糖和2 - 脱氧葡萄糖可通过一个系统转运。对这些解释的支持来自对N - 乙基马来酰胺和环己酰亚胺作用的分析以及竞争实验的结果。葡萄糖的摄取与2 - 脱氧葡萄糖和3 - O - 甲基葡萄糖的摄取有很大不同。糖饥饿的最终结果进一步凸显了这些差异。所研究的转运系统的明显去阻遏现象,为进一步研究各种细胞中转运的调控提供了一个有趣的基础。