Gliemann J, Davidsen O, Sottrup-Jensen L, Sonne O
FEBS Lett. 1985 Sep 2;188(2):352-6. doi: 10.1016/0014-5793(85)80401-4.
Uptake of rat and human alpha 2-macroglobulin-trypsin complexes was measured in rat hepatocytes, rat and human adipocytes and human fibroblasts. Uptake and degradation of 125I-labelled rat complex were about one-third of that of the human complex in the various isolated cell types. In rat hepatocytes, the apparent Km for cell association of the rat complex was about 16 nM as compared to about 6 nM for the human complex. The Vmax values were similar, about 1 X 10(4) molecules X cell-1 X min-1. Thus, rat alpha 2-macroglobulin (an acute-phase protein) complexed with trypsin follows the same pathways of uptake as the human homologue, although with a somewhat lower affinity for the uptake system.
在大鼠肝细胞、大鼠和人脂肪细胞以及人成纤维细胞中测量了大鼠和人α2-巨球蛋白-胰蛋白酶复合物的摄取情况。在各种分离的细胞类型中,125I标记的大鼠复合物的摄取和降解约为人复合物的三分之一。在大鼠肝细胞中,大鼠复合物与细胞结合的表观Km约为16 nM,而人复合物约为6 nM。Vmax值相似,约为1×10(4)分子×细胞-1×分钟-1。因此,与胰蛋白酶复合的大鼠α2-巨球蛋白(一种急性期蛋白)遵循与人同源物相同的摄取途径,尽管对摄取系统的亲和力略低。