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唾液纤连蛋白与口腔链球菌的相互作用。

Interaction of salivary fibronectin with oral streptococci.

作者信息

Babu J P, Dabbous M K

出版信息

J Dent Res. 1986 Aug;65(8):1094-100. doi: 10.1177/00220345860650081001.

DOI:10.1177/00220345860650081001
PMID:3016049
Abstract

Immunoreactive Fibronectin (Fn) has been demonstrated in stimulated human parotid saliva by western blot analysis and also found to be a component of the artificial tooth pellicles derived from hydroxyapatite (HA) beads coated with parotid saliva. Saliva depleted of gelatin-binding components showed a significantly lower degree of reactivity with anti-Fn antibodies than did the control saliva when tested by and enzyme-linked immunosorbent assay (ELISA). Depletion of gelatin-binding components from saliva was also found to affect the degree of saliva-mediated aggregation of four of the seven oral streptococci tested [Streptococcus mutans strains GS-5 and OMZ 176, S. sobrinus, and S. rattus]. Similarly, the adherence of the same four micro-organisms to the artificial tooth pellicles (derived form saliva which had previously been depleted of gelatin-binding component) was significantly inhibited (37-53%) when compared with the control saliva-coated HA beads. Pre-treatment of streptococci with 100 micrograms of soluble Fn also caused a 34-57% inhibition of adherence of the same oral streptococci to saliva-treated HA beads. Quantitation of Fn in human parotid saliva showed that the amounts of immunoreactive Fn varied form 2 to 6 micrograms/mL of parotid saliva. Furthermore, the Fn from parotid saliva was found to be adsorbed onto the bacterial surfaces, as demonstrated by immunofluorescence and ELISA. The presence of Fn in parotid saliva and its ability to bind to HA beads (artificial pellicles), in conjunction with the ability of soluble Fn to inhibit the adherence of streptococcal strains to the artificial tooth pellicles, suggest that the microbial ecology of the oral cavity may, in part, be influenced by the interactions mediated by salivary fibronectin.

摘要

通过蛋白质印迹分析已在刺激后的人腮腺唾液中证实了免疫反应性纤连蛋白(Fn),并且还发现它是源自涂有腮腺唾液的羟基磷灰石(HA)珠的人工牙菌斑的一个组成部分。当通过酶联免疫吸附测定(ELISA)测试时,去除了明胶结合成分的唾液与抗Fn抗体的反应程度明显低于对照唾液。还发现从唾液中去除明胶结合成分会影响所测试的七种口腔链球菌中的四种(变形链球菌菌株GS-5和OMZ 176、远缘链球菌和鼠链球菌)的唾液介导的聚集程度。同样,与对照唾液包被的HA珠相比,这四种微生物对人工牙菌斑(源自先前已去除明胶结合成分的唾液)的黏附受到显著抑制(37%-53%)。用100微克可溶性Fn对链球菌进行预处理也导致相同口腔链球菌对唾液处理过的HA珠的黏附受到34%-57%的抑制。对人腮腺唾液中的Fn进行定量分析表明,免疫反应性Fn的含量在腮腺唾液中为2至6微克/毫升。此外,通过免疫荧光和ELISA证明,腮腺唾液中的Fn被吸附到细菌表面。腮腺唾液中Fn的存在及其与HA珠(人工菌斑)结合的能力,再加上可溶性Fn抑制链球菌菌株对人工牙菌斑黏附的能力,表明口腔的微生物生态可能部分受到唾液纤连蛋白介导的相互作用的影响。

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