Dunn B E, Altmann M, Campbell G P
Laboratory Service, Denver Veterans Administration Medical Center, Colorado.
Rev Infect Dis. 1991 Jul-Aug;13 Suppl 8:S657-64. doi: 10.1093/clinids/13.supplement_8.s657.
An in vitro assay using immunofluorescence and flow cytometry for quantitative assessment of the adherence of Helicobacter pylori to cultured human gastric carcinoma (KATO III) cells was developed. Adherence was rapid, saturable, energy dependent, mannose resistant, and significantly inhibited by fetuin, a glycoprotein containing N-acetylneuraminyllactose. Pretreatment of KATO cells with neuraminidase from Clostridium perfringens, however, did not reduce adherence of H. pylori. Ultrastructurally, adherent cells of H. pylori were associated with indentations of KATO cell membranes. KATO cells should prove useful in the investigation of mechanisms of adherence of H. pylori to mammalian cells. Ultimately, this flow cytometric assay may be helpful in assessment of the adherence of laboratory strains of H. pylori directly to surface mucous cells dissociated from biopsied human gastric tissue.
我们开发了一种体外检测方法,利用免疫荧光和流式细胞术对幽门螺杆菌与培养的人胃癌(KATO III)细胞的黏附进行定量评估。黏附过程迅速、具有饱和性、能量依赖性、对甘露糖不敏感,并且被胎球蛋白(一种含有N - 乙酰神经氨酰乳糖的糖蛋白)显著抑制。然而,用产气荚膜梭菌的神经氨酸酶预处理KATO细胞并不会降低幽门螺杆菌的黏附。在超微结构上,幽门螺杆菌的黏附细胞与KATO细胞膜的凹陷有关。KATO细胞在研究幽门螺杆菌与哺乳动物细胞的黏附机制方面应会被证明是有用的。最终,这种流式细胞术检测方法可能有助于评估幽门螺杆菌实验室菌株与从人胃活检组织中分离出的表面黏液细胞的直接黏附情况。