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牙龈卟啉单胞菌可降低釉基质衍生物对体外牙周膜细胞的作用。

Effect of enamel matrix derivative on periodontal ligament cells in vitro is diminished by Porphyromonas gingivalis.

作者信息

Inaba Hiroaki, Kawai Shinji, Nakayama Koji, Okahashi Nobuo, Amano Atsuo

机构信息

Department of Oral Frontier Biology, Osaka University Graduate School of Dentistry, Suita-Osaka, Japan.

出版信息

J Periodontol. 2004 Jun;75(6):858-65. doi: 10.1902/jop.2004.75.6.858.

Abstract

BACKGROUND

Enamel matrix derivative (EMD) has been shown to possess a mitogenic effect to induce effective periodontal regeneration, however, it is unclear whether periodontal pathogens can modulate the effect of EMD. The present study examined the influence of Porphyromonas gingivalis on EMD-stimulated periodontal ligament (PDL) cells.

METHODS

P. gingivalis ATCC33277 and its mutants deficient in fimbriae (delta fimA) or gingipains (delta rgpA delta rgpB, delta kgp, and delta rgpA delta rgpB delta kgp) were employed. PDL cells were grown on EMD-coated dishes and infected with P. gingivalis wild strain or a mutant. Cell migration and proliferation were then evaluated with an in vitro wound healing assay. The expression of transforming growth factor-beta1 (TGF-beta1) and insulin-like growth factor I (IGF-I) mRNA by PDL cells was examined. Further, the degradation and phosphorylation of extracellular signal-regulated kinase 1 and 2 (ERK1/2) as well as paxillin in infected PDL cells were estimated using Western blot analysis.

RESULTS

P. gingivalis ATCC33277 inhibited the migration and proliferation of PDL cells on EMD-coated dishes, and the mutants delta fimA, delta rgpA delta rgpB, and delta kgp showed the same effects. Further, each of these organisms diminished the expression of TGF-beta1 and IGF-I mRNA, as well as the phosphorylation of ERK1/2 from EMD-stimulated PDL cells. In addition, total paxillin protein was markedly degraded by both the wild-type strain and each of the mutants except for delta rgpA delta rgpB delta kgp, which showed a negligible effect in all of the assays with EMD-stimulated PDL cells.

CONCLUSION

These results suggest that P. gingivalis diminishes the effect of EMD on PDL cells in vitro through a cooperative action of gingipains.

摘要

背景

釉基质衍生物(EMD)已被证明具有促有丝分裂作用,可诱导有效的牙周组织再生,然而,尚不清楚牙周病原体是否能调节EMD的作用。本研究检测了牙龈卟啉单胞菌对EMD刺激的牙周膜(PDL)细胞的影响。

方法

使用牙龈卟啉单胞菌ATCC33277及其菌毛缺陷型突变体(ΔfimA)或牙龈蛋白酶缺陷型突变体(ΔrgpAΔrgpB、Δkgp以及ΔrgpAΔrgpBΔkgp)。将PDL细胞接种于涂有EMD的培养皿上,并感染牙龈卟啉单胞菌野生株或突变体。然后通过体外伤口愈合试验评估细胞迁移和增殖情况。检测PDL细胞中转化生长因子-β1(TGF-β1)和胰岛素样生长因子I(IGF-I)mRNA的表达。此外,采用蛋白质免疫印迹分析评估感染的PDL细胞中细胞外信号调节激酶1和2(ERK1/2)以及桩蛋白的降解和磷酸化情况。

结果

牙龈卟啉单胞菌ATCC33277抑制了涂有EMD的培养皿上PDL细胞的迁移和增殖,菌毛缺陷型突变体ΔfimA、牙龈蛋白酶缺陷型突变体ΔrgpAΔrgpB和Δkgp也表现出相同的作用。此外,这些菌株均降低了TGF-β1和IGF-I mRNA的表达,以及EMD刺激的PDL细胞中ERK1/2的磷酸化水平。另外,野生型菌株和除ΔrgpAΔrgpBΔkgp之外的每个突变体均使总桩蛋白明显降解,而ΔrgpAΔrgpBΔkgp在所有针对EMD刺激的PDL细胞的试验中均显示出可忽略不计的作用。

结论

这些结果表明,牙龈卟啉单胞菌通过牙龈蛋白酶的协同作用在体外减弱了EMD对PDL细胞的作用。

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