Takubo T, Yamane T, Tsuda I, Tagawa S, Tatsumi N
Department of Clinical and Laboratory Medicine, Osaka City University Medical School, Japan.
Br J Biomed Sci. 1997 Dec;54(4):260-6.
The morphology, phagocytic activity, production of hydrogen peroxide (H2O2) and expression of lymphocyte function-associated antigen-1 (LFA-1; CD11a/CD18), complement receptor type 3 (CR3; CD11b/CD18), p150,95 (CD11c/CD18), and platelet/endothelial cell adhesion molecule-1 (PECAM-1; CD31) by oral polymorphonuclear neutrophils (PMN) are assessed and the results compared with those of blood PMN. There were no differences in the morphology and phagocytic activity between oral and blood PMN. H2O2 production was measured following stimulation with phorbol myristate acetate (PMA) and N-formyl-L-leucyl-L-phenylalanine (FMLP) as indicators of bactericidal activity. There was a significant difference in the H2O2 production by the two groups when stimulated with FMLP; the level of H2O2 production by oral PMN was significantly higher than that by blood PMN. However, there was no significant difference in H2O2 production between oral and blood PMN when stimulated with PMA. The percentage of CD11a- and CD11c-positive concentrated oral PMN was significantly lower than that seen in blood PMN, as was the percentage of CD31-positive cells. Higher H2O2 production by oral PMN following stimulation with FMLP may result in enhanced bactericidal activity. Low expression of CD31 may lead to the accumulation of PMN in the mouth by blocking their return to the bloodstream. These phenomena may be necessary for oral PMN to protect periodontal tissues from bacteria in the mouth.
评估口腔多形核中性粒细胞(PMN)的形态、吞噬活性、过氧化氢(H2O2)生成以及淋巴细胞功能相关抗原-1(LFA-1;CD11a/CD18)、补体受体3型(CR3;CD11b/CD18)、p150,95(CD11c/CD18)和血小板/内皮细胞黏附分子-1(PECAM-1;CD31)的表达,并将结果与血液PMN的结果进行比较。口腔和血液PMN在形态和吞噬活性方面没有差异。用佛波醇肉豆蔻酸酯乙酸盐(PMA)和N-甲酰-L-亮氨酰-L-苯丙氨酸(FMLP)作为杀菌活性指标进行刺激后,测量H2O2生成。用FMLP刺激时,两组的H2O2生成存在显著差异;口腔PMN的H2O2生成水平显著高于血液PMN。然而,用PMA刺激时,口腔和血液PMN的H2O2生成没有显著差异。口腔中CD11a和CD11c阳性的集中PMN百分比显著低于血液PMN,CD31阳性细胞的百分比也是如此。FMLP刺激后口腔PMN产生更高的H2O2可能导致杀菌活性增强。CD31的低表达可能通过阻止PMN返回血流而导致其在口腔中积聚。这些现象可能是口腔PMN保护牙周组织免受口腔细菌侵害所必需的。