Galbraith D A, Watts D C
Biochem J. 1981 Apr 1;195(1):221-8. doi: 10.1042/bj1950221.
Acetylcholinesterase was studied in human red cells that had been fractionated on Ficoll/Triosil density gradients into classes representing different ages in vivo. Reticulocytes have negligible acetylcholinesterase activity; this is rapidly acquired on maturation to the erythrocyte. The activity per cell reaches a maximum and then, after a constant period, declines again towards the end of cell life. The maximum activity and the rates of activity gain and loss per cell are quantitatively different in adults and children. Kinetic studies showed that Vmax. follows the same age/activity profile but Km is unaffected by cell age. The acetylcholinesterase protein content, determined by quantitative crossed immunoelectrophoresis, also shows a profile of increase and then decrease with cell age but the specific activity calculated from the protein estimate shows a reverse picture in which there is a slight decrease from young to mid-age cells followed by an increase again in older cells. These results are interpreted to indicate a complex developmental picture in which the overall cell age against enzyme activity profile is determined partly by the amount of enzyme protein present and partly from the modifying effect on the enzyme activity, of interactions with an aging cell membrane.
在通过Ficoll/Triosil密度梯度分离成代表体内不同年龄阶段的类别的人类红细胞中研究了乙酰胆碱酯酶。网织红细胞的乙酰胆碱酯酶活性可忽略不计;在成熟为红细胞时会迅速获得该活性。每个细胞的活性达到最大值,然后在一段稳定期后,在细胞寿命结束时再次下降。每个细胞的最大活性以及活性增加和损失的速率在成人和儿童中在数量上有所不同。动力学研究表明,Vmax遵循相同的年龄/活性曲线,但Km不受细胞年龄的影响。通过定量交叉免疫电泳测定的乙酰胆碱酯酶蛋白含量也显示出随细胞年龄增加然后减少的曲线,但根据蛋白估计值计算的比活性显示出相反的情况,即从年轻细胞到中年细胞略有下降,然后在老年细胞中再次增加。这些结果被解释为表明存在一个复杂的发育情况,其中针对酶活性曲线的整体细胞年龄部分由存在的酶蛋白量决定,部分由与衰老细胞膜相互作用对酶活性的修饰作用决定。