Herráez A, Díez J C, Luque J
Departamento de Bioquímica y Biología Molecular, Universidad de Alcalá, Madrid, Spain.
J Immunol Methods. 1993 Jun 18;162(2):225-34. doi: 10.1016/0022-1759(93)90387-m.
An enzyme-linked immunosorbent assay (ELISA) for the quantitation of rat erythrocyte membrane sialoglycoproteins (glycophorins) has been developed. Samples of erythrocytes and reticulocytes were analysed using this assay, and response compared among them and purified glycophorins samples. A broadly homologous behaviour of glycophorins was found in both cell types, suggesting the presence in reticulocytes of glycophorin molecules closely similar to those on the erythrocyte. A quantitative evaluation of glycophorins on both cell types yielded comparable levels of these glycoproteins, but with significantly higher values (1.7-fold) for reticulocytes. It is suggested that the lower number of epitopes present on the erythrocyte membrane might be due to the disappearance of some glycophorin-associated antigenic determinants during the maturation of reticulocyte to erythrocyte.
已开发出一种用于定量大鼠红细胞膜唾液糖蛋白(血型糖蛋白)的酶联免疫吸附测定(ELISA)法。使用该测定法分析了红细胞和网织红细胞样本,并比较了它们与纯化的血型糖蛋白样本之间的反应。在两种细胞类型中均发现血型糖蛋白具有广泛的同源行为,这表明网织红细胞中存在与红细胞上的血型糖蛋白分子非常相似的分子。对两种细胞类型上的血型糖蛋白进行定量评估,得出这些糖蛋白的水平相当,但网织红细胞的值明显更高(1.7倍)。有人提出,红细胞膜上存在的表位数量较少可能是由于在网织红细胞成熟为红细胞的过程中,一些与血型糖蛋白相关的抗原决定簇消失了。