Feldman S R, Rosenberg M R, Ney K A, Michalopoulos G, Pizzo S V
Biochem Biophys Res Commun. 1985 Apr 30;128(2):795-802. doi: 10.1016/0006-291x(85)90117-2.
The binding of 125I-labeled human alpha 2-macroglobulin-methylamine to adult rat hepatocytes in primary culture was studied at 4 degrees C. Cells which had been in culture for 4 hours exhibited steady state ligand binding after 1 hour, a receptor number of 22,400 receptors per cell, and a dissociation constant of 0.6 nM. Adult rat hepatocytes exhibited a significant decrease in receptor number with increased time in primary culture with less than 10% of the initial number of receptors remaining after 2 days (p less than 0.01). In autopsy studies of mice injected intravenously with 125I-labeled alpha 2-macroglobulin-methylamine, greater than 90% of the cleared ligand was found in the liver. Autoradiography of the liver demonstrated that 80% of the ligand was cleared by hepatocytes. It is concluded that the hepatocytes are the primary pathway for clearance from the circulation of receptor recognized alpha 2-macroglobulin.
在4℃下研究了125I标记的人α2-巨球蛋白-甲胺与原代培养的成年大鼠肝细胞的结合。培养4小时的细胞在1小时后呈现稳态配体结合,每个细胞的受体数量为22,400个,解离常数为0.6 nM。成年大鼠肝细胞在原代培养中随着时间增加受体数量显著减少,2天后剩余的受体数量不到初始数量的10%(p<0.01)。在静脉注射125I标记的α2-巨球蛋白-甲胺的小鼠尸检研究中,发现超过90%的清除配体存在于肝脏中。肝脏的放射自显影表明80%的配体被肝细胞清除。结论是肝细胞是受体识别的α2-巨球蛋白从循环中清除的主要途径。