Christopher C W
J Supramol Struct. 1977;6(4):485-94. doi: 10.1002/jss.400060403.
Hamster (nil) cells maintained overnight in culture medium containing cyclohemiximide and either glucose or fructose exhibit strikingly different rates of hexose transport and metabolism (i.e. uptake). Pretreatment of cultures with sulfhydryl reagents makes it possible to determine initial transport rates for a physiological sugar such as galactose which is a catabolite in hamster cells. Using galactose transport as a model, hexose uptake enhancements can now be shown to be due almost entirely to increases in the rate of the transport step. The transport regulation can best be accounted for by a model comprised of 2 antagonizing mechanism. This model involves turnover of transport carriers as well as inhibitory units ("regulators"). The experimental as well as the theoretical model may also apply to the well-known uptake enhancements observed in oncogenically transformed cells.
在含有环己酰亚胺以及葡萄糖或果糖的培养基中培养过夜的仓鼠(无)细胞,表现出显著不同的己糖转运和代谢(即摄取)速率。用巯基试剂对培养物进行预处理,使得能够确定诸如半乳糖这种在仓鼠细胞中作为分解代谢物的生理性糖的初始转运速率。以半乳糖转运为模型,现在可以表明己糖摄取增强几乎完全是由于转运步骤速率的增加。转运调节最好用一个由两种拮抗机制组成的模型来解释。该模型涉及转运载体以及抑制单元(“调节子”)的周转。实验模型和理论模型也可能适用于在致癌转化细胞中观察到的众所周知的摄取增强现象。