Wadström T, Hirmo S, Novak H, Guzman A, Ringnér-Pantzar M, Utt M, Aleljung P
Department of Medical Microbiology, University of Lund, Sölvegatan 23, Lund S-22362, Sweden.
Curr Microbiol. 1997 May;34(5):267-72. doi: 10.1007/s002849900180.
Helicobacter pylori adhere to Kato III and Hela S3 cells in monolayer cultures. To explore whether cell surface glycoconjugates on these two cell lines mediate binding of H. pylori, various carbohydrates, glycoproteins, and glycolipids were tested to inhibit H.pylori cell adhesion. The adhesion was measured (i) with a urease-based assay and (ii) by cells stained with fluorescein. Sodium periodate and sialidase treatment (but not alpha- or beta-galactosidase, heparitinase,lysozyme, or trypsin) inhibited H. pylori binding to both cell lines. Sulfatides and sulfated glycoconjugates (50 microg/ml) but not heparin or a number of simple carbohydrates inhibited binding (1 mg/ml). The two H.pylori strains studied (CCUG 17874 and strain 25) showed high binding of soluble 125I-labeled heparin and other sulfated carbohydrate compounds.
幽门螺杆菌可黏附于单层培养的加藤III细胞和海拉S3细胞。为探究这两种细胞系表面的糖缀合物是否介导幽门螺杆菌的黏附,对多种碳水化合物、糖蛋白和糖脂进行了测试,以抑制幽门螺杆菌细胞的黏附。采用(i)基于脲酶的检测方法和(ii)用荧光素染色细胞的方法来测定黏附情况。高碘酸钠和唾液酸酶处理(但不是α-或β-半乳糖苷酶、肝素酶、溶菌酶或胰蛋白酶)可抑制幽门螺杆菌与这两种细胞系的结合。硫苷脂和硫酸化糖缀合物(50微克/毫升)可抑制结合,但肝素或多种简单碳水化合物(1毫克/毫升)则不能。所研究的两种幽门螺杆菌菌株(CCUG 17874和25号菌株)对可溶性125I标记的肝素和其他硫酸化碳水化合物化合物表现出高度结合。