Sener A, Malaisse-Lagae F, Malaisse W J
Laboratory of Experimental Medicine, Brussels Free University, Belgium.
Eur J Biochem. 1987 Dec 30;170(1-2):447-52. doi: 10.1111/j.1432-1033.1987.tb13720.x.
In tumoral islet cells (RINm5F line) the phosphorylation of D-fructose is catalyzed by hexokinase rather than fructokinase. Fructose 6-phosphate appears to be preferentially channelled into the pentose cycle, as suggested by a ratio of D-[1-14C]fructose/D-[U-14C]fructose oxidation close to 2.7, the failure to generate 14C-labelled lactate from D-[1-14C]fructose and a poor metabolic response to menadione. When the islet cells are exposed to both D-fructose and D-glucose, however, the metabolism of the former hexose is dramatically modified, fructose 6-phosphate being now formed at a lower rate and preferentially channelled into the glycolytic pathway. These findings illustrate the existence of regulatory steps in fructose catabolism located distally to its site of phosphorylation.
在肿瘤胰岛细胞(RINm5F系)中,D-果糖的磷酸化由己糖激酶而非果糖激酶催化。果糖6-磷酸似乎优先进入戊糖循环,这是由D-[1-14C]果糖/D-[U-14C]果糖氧化比接近2.7、无法从D-[1-14C]果糖生成14C标记的乳酸以及对甲萘醌的代谢反应较差所表明的。然而,当胰岛细胞同时暴露于D-果糖和D-葡萄糖时,前者己糖的代谢会发生显著改变,此时果糖6-磷酸的形成速率较低,并且优先进入糖酵解途径。这些发现说明了果糖分解代谢中位于其磷酸化位点远端的调节步骤的存在。