Boers W, Linthorst C, van Dijk M C, van Berkel T J
Van Gool Laboratory of Experimental Internal Medicine, Academic Medical Center, Amsterdam, The Netherlands.
Ann N Y Acad Sci. 1994 Sep 10;737:428-30. doi: 10.1111/j.1749-6632.1994.tb44331.x.
Serum clearance of alpha 2M-Me or alpha 2M-Tr is rapid and identical. Alpha 2M-Tr is almost exclusively taken up in the liver by the parenchymal cells; the uptake of alpha 2M-Me is equally shared between endothelial and parenchymal cells. Blocking the scavenger receptor on endothelial cells by polyinosinic acid reduces the uptake of alpha 2M-Me to 40% of the control value; under these conditions, alpha 2M-Me is only associated with the parenchymal cells. These results show the following: (1) activation of alpha 2M by methylamine or trypsin is different; (2) the scavenger receptor on endothelial cells functions as a system for the uptake of alpha 2M-Me in addition to the specific alpha 2M receptor on parenchymal cells.
α2M-Me或α2M-Tr的血清清除迅速且相同。α2M-Tr几乎完全被实质细胞摄取到肝脏中;α2M-Me的摄取在内皮细胞和实质细胞之间平均分配。用聚肌苷酸阻断内皮细胞上的清道夫受体会使α2M-Me的摄取降至对照值的40%;在这些条件下,α2M-Me仅与实质细胞相关。这些结果表明:(1)甲胺或胰蛋白酶对α2M的激活不同;(2)除了实质细胞上的特异性α2M受体外,内皮细胞上的清道夫受体还作为α2M-Me的摄取系统发挥作用。