Marynen P, Van Leuven F, Cassiman J J, Van den Berghe H
Biochim Biophys Acta. 1984 Jun 15;799(2):187-93. doi: 10.1016/0304-4165(84)90294-0.
alpha 2-Macroglobulin complexed to proteinases activated during clotting of cystic fibrosis and control sera was quantitated with the complex-specific monoclonal antibody F2B2 . Similar amounts of alpha 2-macroglobulin complexes (between 40 and 90 micrograms/ml) were generated in cystic fibrosis and control sera. Endocytosis of the complexes by normal human fibroblasts was compared to the amount of complexes detected by the F2B2 -radioimmunoassay. Normal uptake was observed with 13 out of 14 cystic fibrosis sera. One cystic fibrosis serum showed strongly reduced endocytosis of the complexes. Complexes isolated from this serum on immobilized F2B2 failed to inhibit binding of purified alpha 2-macroglobulin-trypsin to its receptor, demonstrating deficient receptor-binding of these complexes. The low uptake complexes could not be distinguished from complexes isolated from control or other cystic fibrosis sera by isoelectric focusing, rate electrophoresis or SDS-polyacrylamide gel electrophoresis.
利用复合物特异性单克隆抗体F2B2对与囊性纤维化血清和对照血清凝血过程中激活的蛋白酶结合的α2-巨球蛋白进行定量。囊性纤维化血清和对照血清中产生的α2-巨球蛋白复合物量相似(40至90微克/毫升之间)。将正常人成纤维细胞对这些复合物的内吞作用与F2B2放射免疫测定法检测到的复合物量进行比较。14份囊性纤维化血清中有13份观察到正常摄取。一份囊性纤维化血清显示复合物的内吞作用大幅降低。从该血清中通过固定化F2B2分离出的复合物未能抑制纯化的α2-巨球蛋白-胰蛋白酶与其受体的结合,表明这些复合物的受体结合存在缺陷。通过等电聚焦、速率电泳或SDS-聚丙烯酰胺凝胶电泳,无法将低摄取复合物与从对照血清或其他囊性纤维化血清中分离出的复合物区分开来。