Dini L, Conti-Devirgiliis L, Russo-Caia S
Department of Biology, University of Rome, Tor Vergata, Italy.
Development. 1987 May;100(1):13-22. doi: 10.1242/dev.100.1.13.
The number and distribution of galactose-specific binding sites were investigated in rat liver cells during perinatal development. Ligand binding to hepatocytes, macrophages and endothelial cells was followed with in vitro and in situ experiments by electron microscopy, using lactosylated bovine serum albumin adsorbed onto 5 nm colloidal gold particles as ligand. Binding capacity, starting at a late stage of fetal development, is very low both on the hepatocyte and on the macrophage surface, which show single particles statistically distributed. By contrast, bound particles are absent from fetal endothelial cells, which also lack the typical coated regions. In vivo, experiments at 37 degrees C show that endocytosis occurs to some extent in prenatal life. These results indicate that the expression of galactose-specific receptors' activity on the different liver cell types follows different developmental patterns, which are independently modulated.
在围产期发育过程中,对大鼠肝细胞中半乳糖特异性结合位点的数量和分布进行了研究。使用吸附在5纳米胶体金颗粒上的乳糖基化牛血清白蛋白作为配体,通过体外和原位电子显微镜实验跟踪配体与肝细胞、巨噬细胞和内皮细胞的结合情况。从胎儿发育后期开始,肝细胞和巨噬细胞表面的结合能力都非常低,表面的单个颗粒呈统计分布。相比之下,胎儿内皮细胞缺乏结合颗粒,也没有典型的包被区域。在体内,37摄氏度的实验表明,内吞作用在产前生活中会在一定程度上发生。这些结果表明,不同肝细胞类型上半乳糖特异性受体活性的表达遵循不同的发育模式,且这些模式是独立调节的。