Literature DB >> 17559633

Lipid A-associated proteins from Porphyromonas gingivalis stimulate release of nitric oxide by inducing expression of inducible nitric oxide synthase.

E-Y Choi1, Y-M Hwang, J-Y Lee, J-I Choi, I-S Choi, J-Y Jin, J S Ko, S-J Kim.   

Abstract

BACKGROUND AND
OBJECTIVE: The purpose of this study was to examine the effects of lipid A-associated proteins from Porphyromonas gingivalis, a major cause of inflammatory periodontal disease, on the production of nitric oxide and expression of inducible nitric oxide synthase in the murine macrophage cell line, RAW264.7. We also attempted to throw light on the signaling mechanisms involved in P. gingivalis lipid A-associated protein-induced nitric oxide production.
MATERIAL AND METHODS: The lipid A-associated proteins from P. gingivalis 381 were prepared by standard hot phenol-water extraction of endotoxin isolated by the butanol method. Nitric oxide production was assayed by measuring the accumulation of nitrite in culture supernatants. Western blot analysis of inducible nitric oxide synthase and analysis of reverse transcription-polymerase chain reaction products were carried out.
RESULTS: We found that P. gingivalis lipid A-associated proteins can induce inducible nitric oxide synthase expression and stimulate the release of nitric oxide without additional stimuli, and we demonstrated that multiple signaling pathways, such as nuclear factor-kappaB, microtubule polymerization, protein tyrosine kinase, protein kinase C, and mitogen-activated protein kinase cascades, are involved in P. gingivalis lipid A-associated protein-stimulated nitric oxide production. The production of nitric oxide required l-arginine.
CONCLUSION: The present study clearly shows that P. gingivalis lipid A-associated proteins fully induced inducible nitric oxide synthase expression and nitric oxide production in RAW264.7 cells in the absence of other stimuli. The ability of P. gingivalis lipid A-associated proteins to promote the production of nitric oxide may be important in the pathogenesis of inflammatory periodontal disease.

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Year:  2007        PMID: 17559633     DOI: 10.1111/j.1600-0765.2006.00956.x

Source DB:  PubMed          Journal:  J Periodontal Res        ISSN: 0022-3484            Impact factor:   4.419


  4 in total

1.  Porphyromonas gingivalis, gamma interferon, and a proapoptotic fibronectin matrix form a synergistic trio that induces c-Jun N-terminal kinase 1-mediated nitric oxide generation and cell death.

Authors:  Abhijit Ghosh; Ji Young Park; Christopher Fenno; Yvonne L Kapila
Journal:  Infect Immun       Date:  2008-10-06       Impact factor: 3.441

2.  Morphologic evaluation and expression of matrix metalloproteinases-2 and 9 and nitric oxide during experimental periodontal disease in rat.

Authors:  Camila Oliveira Rodini; Aline Carvalho Batista; Thiago José Dionísio; Carlos Ferreira Santos; Fernando Queiroz Cunha; Vanessa Soares Lara
Journal:  J Mol Histol       Date:  2008-02-05       Impact factor: 2.611

3.  Heterogeneous Porphyromonas gingivalis LPS modulates immuno-inflammatory response, antioxidant defense and cytoskeletal dynamics in human gingival fibroblasts.

Authors:  Thanuja D K Herath; Richard P Darveau; Chaminda J Seneviratne; Cun-Yu Wang; Yu Wang; Lijian Jin
Journal:  Sci Rep       Date:  2016-08-19       Impact factor: 4.379

4.  Effects of β-Glucan on the Release of Nitric Oxide by Macrophages Stimulated with Lipopolysaccharide.

Authors:  E Y Choi; S S Lee; J Y Hyeon; S H Choe; B R Keum; J M Lim; D C Park; I S Choi; K K Cho
Journal:  Asian-Australas J Anim Sci       Date:  2016-07-29       Impact factor: 2.509

  4 in total

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