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论文摘要

不同fimA基因型牙龈卟啉单胞菌刺激中性粒细胞产生基质金属蛋白酶8和9的比较

Matrix metalloproteinase 8 and 9 regulations of polymorphonuclear leukocytes stimulated by Porphyromonas gingivalis with different fimA genotypes

作者:欧阳玉玲 吴亚菲 赵蕾 肖晓蓉 张静仪 李小玉

Author:OUYANG Yu -ling1, WU Ya -fei2, ZHAO Lei1, XIAO Xiao -rong1, ZHANG Jing-yi1, LI Xiao-yu1

收稿日期:2009-04-25          年卷(期)页码:2009,27(02):206-

期刊名称:华西口腔医学杂志

Journal Name:West China Journal of Stomatology

关键字:牙龈卟啉单胞菌,中性粒细胞,基质金属蛋白酶,

Key words:Porphyromonas gingivalis,polymorphonuclear leukocyte,matrix metalloproteinase,

基金项目:

国家自然科学基金资助项目(30471890)

中文摘要

目的比较不同fimA基因型牙龈卟啉单胞菌(P.gingivalis)刺激下人外周血中性粒细胞(PMNs)产生基质金属蛋白酶8、9(MMP-8、MMP-9)的差异。方法采用密度梯度离心分离法分离纯化培养PMNs,P.gingivalis ATCC33277(ⅠfimA)、WCSP 115(ⅡfimA)、WCSP 1.5(ⅢfimA)、W83(ⅣfimA)、WCSP 559(ⅣfimA)菌悬液与新鲜分离的PMNs悬液共孵育2 h,于5 min、30 min、1 h、2 h收集上清液,用ELISA方法检测MMP-8、MMP-9的表达。结果不同fimA基因型P.gingivalis刺激PMNs产生MMP-8、MMP-9的能力都显著高于未受刺激组;ⅡfimA、ⅣfimA(W83)型P.gingivalis刺激PMNs分泌MMP-8在速度及量上均高于ⅢfimA、ⅣfimA(WCSP 559)型P.gingivalis;ⅠfimA、ⅡfimA、ⅣfimA(W83)型P.gingivalis刺激PMNs分泌MMP-9能力高于ⅢfimA、ⅣfimA(WCSP 559)型P.gingivalis。结论ⅡfimA、ⅣfimA型P.gingivalis的致病能力相对较强,提示P.gingivalis的毒力和致病性与fimA基因型存在相关性。

英文摘要

Objective To investigate the pathogenicity of matrix metalloproteinase 8, 9(MMP-8, MMP-9) regulations of polymorphonuclear leukocytes(PMNs) by challenge of Porphyromonas gingivalis(P.gingivalis) with different fimA genotypes. Methods The studies mainly adopt the isopycnic sedimentation separation to separate the PMNs from human peripheral blood. P.gingivalis ATCC 33277(typeⅠ),WCSP 115(typeⅡ),WCSP 1.5(typeⅢ),W83(typeⅣ), WCSP 559(typeⅣ) were assessed for their inductions of MMP-8, MMP-9 expression in PMNs. MMP-8, MMP-9 protein levels in culture supernatant were determined by ELISA at different time intervals(5 min, 30 min, 1 h, 2 h) following continuous co-culture of bacteria with PMNs. Results MMP-8 and MMP-9 protein levels produced by PMNs co-culture with the ⅠfimA—ⅣfimA P.gingivalis were significantly stronger than unsimulated group. The velocity and quantity of MMP-8 produced by PMNs co-culture with the ⅡfimA P.gingivalis and ⅣfimA P.gingivalis were more than ⅢfimA, ⅣfimA P.gingivalis. The MMP-9 protein levels produced by PMNs co-culture with the ⅠfimA, ⅡfimA, ⅣfimA P.gingivalis was significantly stronger than ⅢfimA and ⅣfimA P.gingivalis. Conclusion Ⅱ fimA and ⅣfimA P.gingivalis have stronger pathogenicity relatively, which indicate that fimA genotype is associated with pathogenesis of P.gingivalis.

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