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Effect of Enamel Matrix Derivative on Periodontal Ligament Cells In Vitro Is Diminished by Porphyromonas gingivalis
Author(s) -
Inaba Hiroaki,
Kawai Shinji,
Nakayama Koji,
Okahashi Nobuo,
Amano Atsuo
Publication year - 2004
Publication title -
journal of periodontology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.036
H-Index - 156
eISSN - 1943-3670
pISSN - 0022-3492
DOI - 10.1902/jop.2004.75.6.858
Subject(s) - enamel matrix derivative , porphyromonas gingivalis , periodontal fiber , in vitro , dentistry , enamel paint , chemistry , matrix (chemical analysis) , tooth enamel , periodontitis , medicine , biology , microbiology and biotechnology , biochemistry , regeneration (biology) , chromatography
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 ( ΔfimA ) or gingipains ( ΔrgpA ΔrgpB, Δkgp , and ΔrgpAΔrgpB Δkgp ) were employed. PDL cells were grown on EMDcoated 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‐ β1 (TGF‐β1) 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 ΔfimA, ΔrgpAΔrgpB , and Δkgp showed the same effects. Further, each of these organisms diminished the expression of TGF‐β1 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 ΔrgpAΔrgpBΔkgp , 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. J Periodontol 2004;75:858‐865 .