[Home ] [Archive]    
:: Main :: About :: Current Issue :: Archive :: Search :: Submit ::
Main Menu
Journal Information::
Editorial Policies::
Articles archive::
For Authors::
Contact us::
Site Facilities::
::
Search in website

Advanced Search
Receive site information
Enter your Email in the following box to receive the site news and information.
Last site contents
:: Contact Us
:: Volume 35, Issue 3 And 4 (10-2023) ::
J Iran Dent Assoc 2023, 35(3 And 4): 64-72 Back to browse issues page
The effect of lipopolysaccharide contamination on gutta percha induced TNF-alpha and IL-1 beta gene expression by human monocyte cells
Hadi Assadian1 , Nassim Hashemi * 2, Abdollah Ghorbanzadeh3 , Maryam Nourizadeh4 , Jamshid Hadjati5
1- Assistant Professor, Department of Endodontics, School of Dentistry, Tehran University of Medical Sciences (TUMS), Tehran, IR Iran
2- Postgraduate Student, Department of Endodontics, School of Dentistry, Tehran University of Medical Sciences (TUMS), Tehran, IR Iran , nsm.hashemi@gmail.com
3- Department of Endodontics, School of Dentistry, Tehran University of Medical Sciences (TUMS), Tehran, IR Iran
4- Assistant Professor of Medical Immunology, Immunology, Asthma and Allergy Research Institute, Tehran, IR Iran
5- Professor of Medical Immunology, Department of Immunology, School of Medicine, Autoimmune Bullous Diseases Research Center, Tehran University of Medical Sciences (TUMS), Tehran, IR Iran
Abstract:   (142 Views)
Background and Aim: The aim of this study was to assess gutta percha-induced TNF-alpha and IL-1 beta gene expression in the presence or absence of bacterial lipo-polysaccharide (LPS) on cultured human monocyte cells in vitro.
Materials and Methods: Human monocytes from THP-1 cell line were cultured. Standardized gutta percha segments were prepared and directly placed at the bottom of the culture wells. Cultured cells were exposed to the materials in G1 and G2 groups and then LPS was added only to G1. Positive control included the bacterial LPS without the gutta percha segments and the negative control contained the cells in culture medium only. TNF-alpha and IL1-beta gene expression was evaluated using RT-PCR technique. Data were statistically analyzed using Kruskal-Wallis and Bonferroni-adjusted post-hoc tests.
Results: A statistically significant difference was noted between LPS-treated and un-treated groups regarding IL-1-beta and TNF-alpha gene expression (p < 0.05). In G2 (the gutta-percha without LPS), IL-1-beta, and TNF-alpha gene expression was signifi-cantly higher compared to the negative control group (p < 0.05). In G1 (gutta-percha with LPS), TNF-alpha and IL-1-beta gene expression was significantly higher than in the positive control group (p<0.05).
Conclusion: It was indicated that gutta-percha could induce the expression of pro-inflammatory cytokines TNF-alpha and IL-1-beta, with this effect being significantly magnified by LPS contamination.
Keywords: Gutta-Percha, Lipopolysaccharides, Tumor Necrosis Factor-alpha, Interleukin-1-beta, Monocytes Cell Line, Gene Expression, Polymerase Chain Reaction, Inflammation Mediators, Endodontics
Full-Text [PDF 643 kb]   (81 Downloads)    
Type of Study: Original | Subject: Endodontics
Send email to the article author

Add your comments about this article
Your username or Email:

CAPTCHA


XML     Print


Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:

Assadian H, Hashemi N, Ghorbanzadeh A, Nourizadeh M, Hadjati J. The effect of lipopolysaccharide contamination on gutta percha induced TNF-alpha and IL-1 beta gene expression by human monocyte cells. J Iran Dent Assoc 2023; 35 (3 and 4) :64-72
URL: http://jida.ir/article-1-2247-en.html


Rights and permissions
Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
Volume 35, Issue 3 And 4 (10-2023) Back to browse issues page
Journal of Iranian Dental Association

AWT IMAGE

This work is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License which allows users to read, copy, distribute and make derivative works for non-commercial purposes from the material, as long as the author of the original work is cited properly

Persian site map - English site map - Created in 0.05 seconds with 37 queries by YEKTAWEB 4660