Keitt A S
J Clin Invest. 1969 Nov;48(11):1997-2007. doi: 10.1172/JCI106165.
Analyses of key glycolytic intermediates in freshly drawn red cells from six related individuals suggest that decreased hexokinase activity underlies the hemolytic process in the two members with overt hemolysis. Low red cell glucose 6-phosphate (G6P) was observed not only in the anemic patients but in the presumptive heterozygotes as well and served as a useful marker for the presence of the trait. Hexokinase activity was labile in distilled water hemolysates but was only slightly low when protected by glucose, mercaptoethanol, and ethylenediaminetetraacetate (EDTA). Normal red cell hexokinase was demonstrated to be dependent on glucose for maintenance of activity after heating to 45 degrees C. The cells of the proposita are unable to utilize glucose efficiently at glucose concentrations lower than 0.2 mmole/liter whereas normal cells maintain linear glucose consumption to at least 0.05 mM glucose. These qualitative abnormalities could result from the presence of a mutant hexokinase with an abnormally reactive sulfhydryl group and altered substrate affinity in the red cells of this kindred.
对来自六个相关个体的新鲜抽取红细胞中的关键糖酵解中间体进行分析表明,己糖激酶活性降低是两名有明显溶血症状成员溶血过程的基础。不仅在贫血患者中,而且在推定的杂合子中也观察到红细胞葡萄糖6-磷酸(G6P)水平较低,它可作为该性状存在的有用标志物。己糖激酶活性在蒸馏水溶血产物中不稳定,但在有葡萄糖、巯基乙醇和乙二胺四乙酸(EDTA)保护时仅略低。正常红细胞己糖激酶在加热至45摄氏度后被证明依赖葡萄糖来维持活性。先证者的细胞在葡萄糖浓度低于0.2毫摩尔/升时无法有效利用葡萄糖,而正常细胞在葡萄糖浓度至少为0.05毫摩尔/升时仍保持线性葡萄糖消耗。这些定性异常可能是由于该家族红细胞中存在具有异常反应性巯基基团和改变底物亲和力的突变己糖激酶所致。