Kobayashi A, Kobayashi K, Akaike T
Kanagawa Academy of Science and Technology, Kawasaki, Japan.
J Biomater Sci Polym Ed. 1992;3(6):499-508. doi: 10.1163/156856292x00466.
Adhesion of hepatocytes on culture dishes whose surface was coated with a lactose-carrying styrene homopolymer (PVLA) was investigated. Hepatocytes maintained their round shape on PVLA substratum, which is in contrast to the usual spread shape characteristic of those cultured on collagen and fibronectin substrata. Calcium ion was indispensable for hepatocyte adhesion in PVLA substratum, and hence the hepatocytes on PVLA were easily detached when the culture was treated with ethylenediamine tetraacetic acid (EDTA). The recovered hepatocytes readheres to PVLA. The adhesion of hepatocytes to PVLA was not inhibited by cytochalasin B but by colchicine. Hepatocytes recognize the galactose moieties on the surface of asialoglycoproteins and removes these proteins from the blood stream by receptor mediated endocytosis. The mechanism of adhesion of hepatocytes on PVLA substratum which contains a high density of galactose residues was distinct from the attachment on collagen and fibronectin substrata, and showed great similarity to the receptor and ligand interactions which occurs in the clearance of asialoglycoproteins by hepatocytes.
研究了肝细胞在表面涂有含乳糖苯乙烯均聚物(PVLA)的培养皿上的黏附情况。肝细胞在PVLA基质上保持圆形,这与在胶原蛋白和纤连蛋白基质上培养的肝细胞通常呈现的铺展形状形成对比。钙离子对于肝细胞在PVLA基质上的黏附是必不可少的,因此当用乙二胺四乙酸(EDTA)处理培养物时,PVLA上的肝细胞很容易脱落。回收的肝细胞会重新黏附到PVLA上。细胞松弛素B不会抑制肝细胞与PVLA的黏附,但秋水仙碱会抑制。肝细胞识别去唾液酸糖蛋白表面的半乳糖部分,并通过受体介导的内吞作用将这些蛋白质从血流中清除。肝细胞在含有高密度半乳糖残基的PVLA基质上的黏附机制与在胶原蛋白和纤连蛋白基质上的附着不同,并且与肝细胞清除去唾液酸糖蛋白过程中发生的受体与配体相互作用非常相似。