Literature DB >> 33128253

Porphyromonas gingivalis infection alters Nrf2-phase II enzymes and nitric oxide in primary human aortic endothelial cells.

Chethan Sampath1, Emmanuel U Okoro2, Michael J Gipson1, Sasanka S Chukkapalli3, Cherae M Farmer-Dixon1, Pandu R Gangula1.   

Abstract

BACKGROUND: Periodontal disease (PD) is known to be associated with endothelial dysfunction in patients with coronary artery and/or cardiovascular disease. In our study, we sought to explore the virulence of P. gingivalis (Pg) affecting glycogen synthase kinase 3 beta (GSK-3β)/nuclear factor (erythroid-derived 2)-like 2 (Nrf2)/tetrahydrobiopterin (BH4 )/ nitric oxide synthase (NOS) expression in primary human aortic endothelial cells (pHAECs).
METHODS: pHAECs were infected for 48 hours with Pg in vitro using the Human oxygen-Bacteria anaerobic coculture technique. Cell viability was determined, and target gene expression changes were evaluated by quantitative real-time polymerase chain reaction at the end of each incubation period.
RESULTS: Pg impaired pHAEC viability 24 hours post-infection. Pg infection reduced mRNA expression levels of endothelial NOS (eNOS), Nrf2, and Phase II enzymes (heme oxygenase-1, catalase, superoxide dismutase-1) in a time-dependent manner. Significant (P <0.05) increase in the inflammatory markers (interleukin [IL]-1β, IL-6, and tumor necrosis factor-α) were observed in the medium as well as in the infected cells. Interestingly, inducible NOS mRNA levels showed a significant (P <0.05) increase at 12 hours and 24 hours and were reduced at later time points. BH4 (cofactor of eNOS) biosynthesis enzyme dihydrofolate reductase (DHFR, salvage pathway) mRNA levels showed a significant (P <0.05) decrease, while mRNA levels of GSK-3β were elevated.
CONCLUSIONS: These results suggest that periodontal bacterial infection may cause significant changes in the endothelial GSK-3β/BH4 /eNOS/Nrf2 pathways, which may lead to impaired vascular relaxation. Greater understanding of the factors that adversely affect endothelial cell function could contribute to the development of new therapeutic compounds to treat PD-induced vascular diseases.
© 2020 American Academy of Periodontology.

Entities:  

Keywords:  GSK-3β; NOS; Nrf2; P. gingivalis; periodontal disease; primary human aortic endothelial cells

Mesh:

Substances:

Year:  2020        PMID: 33128253      PMCID: PMC8085184          DOI: 10.1002/JPER.20-0444

Source DB:  PubMed          Journal:  J Periodontol        ISSN: 0022-3492            Impact factor:   6.993


  49 in total

1.  Deficiency of iNOS contributes to Porphyromonas gingivalis-induced tissue damage.

Authors:  J Alayan; S Ivanovski; E Gemmell; P Ford; S Hamlet; C S Farah
Journal:  Oral Microbiol Immunol       Date:  2006-12

2.  Porphyromonas gingivalis is the most abundant species detected in coronary and femoral arteries.

Authors:  J-L C Mougeot; C B Stevens; B J Paster; M T Brennan; P B Lockhart; F K B Mougeot
Journal:  J Oral Microbiol       Date:  2017-02-08       Impact factor: 5.474

Review 3.  Bacterial invasion and persistence: critical events in the pathogenesis of periodontitis?

Authors:  S Ji; Y S Choi; Y Choi
Journal:  J Periodontal Res       Date:  2014-12-08       Impact factor: 4.419

4.  Porphyromonas gingivalis as a Model Organism for Assessing Interaction of Anaerobic Bacteria with Host Cells.

Authors:  Christopher M Wunsch; Janina P Lewis
Journal:  J Vis Exp       Date:  2015-12-17       Impact factor: 1.355

5.  Dihydrofolate reductase protects endothelial nitric oxide synthase from uncoupling in tetrahydrobiopterin deficiency.

Authors:  Mark J Crabtree; Ashley B Hale; Keith M Channon
Journal:  Free Radic Biol Med       Date:  2011-03-12       Impact factor: 7.376

6.  A key role for tetrahydrobiopterin-dependent endothelial NOS regulation in resistance arteries: studies in endothelial cell tetrahydrobiopterin-deficient mice.

Authors:  Surawee Chuaiphichai; Mark J Crabtree; Eileen Mcneill; Ashley B Hale; Lucy Trelfa; Keith M Channon; Gillian Douglas
Journal:  Br J Pharmacol       Date:  2017-03-13       Impact factor: 8.739

7.  A simple coculture system shows mutualism between anaerobic faecalibacteria and epithelial Caco-2 cells.

Authors:  Mehdi Sadaghian Sadabad; Julius Z H von Martels; Muhammed Tanweer Khan; Tjasso Blokzijl; Giuseppe Paglia; Gerard Dijkstra; Hermie J M Harmsen; Klaas Nico Faber
Journal:  Sci Rep       Date:  2015-12-15       Impact factor: 4.379

8.  Active invasion of oral and aortic tissues by Porphyromonas gingivalis in mice causally links periodontitis and atherosclerosis.

Authors:  Irina M Velsko; Sasanka S Chukkapalli; Mercedes F Rivera; Ju-Youn Lee; Hao Chen; Donghang Zheng; Indraneel Bhattacharyya; Pandu R Gangula; Alexandra R Lucas; Lakshmyya Kesavalu
Journal:  PLoS One       Date:  2014-05-16       Impact factor: 3.240

9.  Porphyromonas gingivalis lipopolysaccharides act exclusively through TLR4 with a resilience between mouse and human.

Authors:  Brice Nativel; David Couret; Pierre Giraud; Olivier Meilhac; Christian Lefebvre d'Hellencourt; Wildriss Viranaïcken; Christine Robert Da Silva
Journal:  Sci Rep       Date:  2017-11-17       Impact factor: 4.379

Review 10.  The Role of Nrf2 in Cardiovascular Function and Disease.

Authors:  Sandro Satta; Ayman M Mahmoud; Fiona L Wilkinson; M Yvonne Alexander; Stephen J White
Journal:  Oxid Med Cell Longev       Date:  2017-09-14       Impact factor: 6.543

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  1 in total

Review 1.  The Effects of Porphyromonas gingivalis on Atherosclerosis-Related Cells.

Authors:  Jiaqi Zhang; Mengru Xie; Xiaofei Huang; Guangjin Chen; Ying Yin; Xiaofeng Lu; Guangxia Feng; Ran Yu; Lili Chen
Journal:  Front Immunol       Date:  2021-12-23       Impact factor: 7.561

  1 in total

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