Zentner A, Heaney T G
Department of Orthodontics, School of Dentistry, University of Mainz, Germany.
Eur J Oral Sci. 1996 Oct-Dec;104(5-6):634-6. doi: 10.1111/j.1600-0722.1996.tb00155.x.
The aim of this study was to determine whether human high molecular weight salivary glycoprotein binds in vitro to human gingival fibroblast-like cells. Primary monolayer cultures of 2 human gingival fibroblast-like cell lines were incubated with a high molecular weight fraction of salivary glycoprotein which expressed blood group A activity and glycoprotein-cell binding probed using an FITC-conjugated mouse monoclonal antibody to human blood group A antigen. Surface fluorescence of protein-treated cells was found to be no greater than that of untreated or serum-treated control cultures. As significant binding of salivary glycoprotein to gingival fibroblast-like cells does not occur in vitro, saliva-mediated inhibition of fibroblast attachment to hydroxyapatite is not dependent on specific ligand-lectin interactions.
本研究的目的是确定人高分子量唾液糖蛋白在体外是否与人牙龈成纤维样细胞结合。将2种人牙龈成纤维样细胞系的原代单层培养物与表达A血型活性的唾液糖蛋白高分子量组分一起孵育,并用针对人A血型抗原的异硫氰酸荧光素(FITC)偶联小鼠单克隆抗体探测糖蛋白与细胞的结合。发现经蛋白处理的细胞的表面荧光不高于未处理或经血清处理的对照培养物。由于唾液糖蛋白在体外不会与人牙龈成纤维样细胞发生显著结合,因此唾液介导的成纤维细胞对羟基磷灰石附着的抑制不依赖于特定的配体-凝集素相互作用。