Jonas L, Walzel H, Bremer H, Wiedlocha A
Department of Pathology, University of Rostock, Germany.
Acta Histochem. 1992;92(1):46-53. doi: 10.1016/S0065-1281(11)80140-6.
Using a preembedding electron microscopic technique, the binding and internalization of gold labelled mistletoe lectin I (MLI.Au), its 2 A subunits (MLI-A.Au) and of the B subunit (MLI-B.Au) in murine L 1210V leukemia cells was analysed. Furthermore, the endocytosis of a gold marked immunotoxin (MoAb-16-MLI-A.Au), consisting of a monoclonal antibody (MoAb-16) reacting with L 1210V cells and the cytotoxic A subunits (MLI-A) was detected. The cells were incubated with MLI.Au, MLI-A.Au, MLI-B.Au, or MoAb-16-MLI-A.Au at 37 degrees C for 1, 3, 5, 10, 20 or 30 min, respectively. Remarkable differences were found in the endocytotic pathway and internalization kinetics. The endocytosis of MLI, its subunits and of the immunotoxin has been compared to that of the other ligands in various systems.
采用预包埋电子显微镜技术,分析了金标记的槲寄生凝集素I(MLI.Au)、其2个A亚基(MLI-A.Au)和B亚基(MLI-B.Au)在小鼠L 1210V白血病细胞中的结合和内化情况。此外,还检测了一种金标记免疫毒素(MoAb-16-MLI-A.Au)的内吞作用,该免疫毒素由与L 1210V细胞反应的单克隆抗体(MoAb-16)和细胞毒性A亚基(MLI-A)组成。将细胞分别与MLI.Au、MLI-A.Au、MLI-B.Au或MoAb-16-MLI-A.Au在37℃下孵育1、3、5、10、20或30分钟。在内吞途径和内化动力学方面发现了显著差异。已将MLI及其亚基以及免疫毒素的内吞作用与各种系统中其他配体的内吞作用进行了比较。