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Periodontal CD14 mRNA expression is downregulated in patients with chronic periodontitis and type 2 diabetes
BACKGROUND: Patients with type 2 diabetes mellitus (T2DM) have increased severity of periodontitis. Toll-like receptor (TLR)4, its co-receptors CD14 and MD-2, and adaptor MyD88 play pivotal roles in lipopolysaccharide (LPS)-triggered tissue inflammation and periodontitis. This study investigated the...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4652420/ https://www.ncbi.nlm.nih.gov/pubmed/26581717 http://dx.doi.org/10.1186/s12903-015-0118-3 |
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author | Hedgpeth, Dustin C. Zhang, Xiaoming Jin, Junfei Leite, Renata S. Krayer, Joe W. Huang, Yan |
author_facet | Hedgpeth, Dustin C. Zhang, Xiaoming Jin, Junfei Leite, Renata S. Krayer, Joe W. Huang, Yan |
author_sort | Hedgpeth, Dustin C. |
collection | PubMed |
description | BACKGROUND: Patients with type 2 diabetes mellitus (T2DM) have increased severity of periodontitis. Toll-like receptor (TLR)4, its co-receptors CD14 and MD-2, and adaptor MyD88 play pivotal roles in lipopolysaccharide (LPS)-triggered tissue inflammation and periodontitis. This study investigated the effects of T2DM and periodontitis on TLR4, CD14, MD-2 and MyD88 mRNA expression in surgically removed periodontal tissues. METHODS: Periodontal tissue specimens were collected from 14 patients without periodontitis and T2DM (Group 1), 15 patients with periodontitis alone (Group 2), and 7 patients with both periodontitis and T2DM (Group 3). The mRNA of TLR4, CD14, MD-2 and MyD88 was quantified using real-time PCR and compared between the groups. RESULTS: Statistical analysis showed that periodontal expression of CD14 mRNA was significantly reduced across Groups 1, 2 and 3 (p = 0.02) whereas the mRNA expression of TLR4, MD-2 and MyD88 was not significantly different among the groups. Furthermore, when patients in Groups 1 and 2 were combined (n = 22), the CD14 mRNA expression was significantly lower than that in patients of Group 1 (p = 0.04). CONCLUSIONS: CD14 mRNA expression was downregulated across patients with neither periodontitis nor T2DM, patients with periodontitis alone and patients with both diseases, suggesting that CD14 mRNA expression is associated with a favorable host response or subjected to a negative feedback regulation. |
format | Online Article Text |
id | pubmed-4652420 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-46524202015-11-20 Periodontal CD14 mRNA expression is downregulated in patients with chronic periodontitis and type 2 diabetes Hedgpeth, Dustin C. Zhang, Xiaoming Jin, Junfei Leite, Renata S. Krayer, Joe W. Huang, Yan BMC Oral Health Research Article BACKGROUND: Patients with type 2 diabetes mellitus (T2DM) have increased severity of periodontitis. Toll-like receptor (TLR)4, its co-receptors CD14 and MD-2, and adaptor MyD88 play pivotal roles in lipopolysaccharide (LPS)-triggered tissue inflammation and periodontitis. This study investigated the effects of T2DM and periodontitis on TLR4, CD14, MD-2 and MyD88 mRNA expression in surgically removed periodontal tissues. METHODS: Periodontal tissue specimens were collected from 14 patients without periodontitis and T2DM (Group 1), 15 patients with periodontitis alone (Group 2), and 7 patients with both periodontitis and T2DM (Group 3). The mRNA of TLR4, CD14, MD-2 and MyD88 was quantified using real-time PCR and compared between the groups. RESULTS: Statistical analysis showed that periodontal expression of CD14 mRNA was significantly reduced across Groups 1, 2 and 3 (p = 0.02) whereas the mRNA expression of TLR4, MD-2 and MyD88 was not significantly different among the groups. Furthermore, when patients in Groups 1 and 2 were combined (n = 22), the CD14 mRNA expression was significantly lower than that in patients of Group 1 (p = 0.04). CONCLUSIONS: CD14 mRNA expression was downregulated across patients with neither periodontitis nor T2DM, patients with periodontitis alone and patients with both diseases, suggesting that CD14 mRNA expression is associated with a favorable host response or subjected to a negative feedback regulation. BioMed Central 2015-11-18 /pmc/articles/PMC4652420/ /pubmed/26581717 http://dx.doi.org/10.1186/s12903-015-0118-3 Text en © Hedgpeth et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Hedgpeth, Dustin C. Zhang, Xiaoming Jin, Junfei Leite, Renata S. Krayer, Joe W. Huang, Yan Periodontal CD14 mRNA expression is downregulated in patients with chronic periodontitis and type 2 diabetes |
title | Periodontal CD14 mRNA expression is downregulated in patients with chronic periodontitis and type 2 diabetes |
title_full | Periodontal CD14 mRNA expression is downregulated in patients with chronic periodontitis and type 2 diabetes |
title_fullStr | Periodontal CD14 mRNA expression is downregulated in patients with chronic periodontitis and type 2 diabetes |
title_full_unstemmed | Periodontal CD14 mRNA expression is downregulated in patients with chronic periodontitis and type 2 diabetes |
title_short | Periodontal CD14 mRNA expression is downregulated in patients with chronic periodontitis and type 2 diabetes |
title_sort | periodontal cd14 mrna expression is downregulated in patients with chronic periodontitis and type 2 diabetes |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4652420/ https://www.ncbi.nlm.nih.gov/pubmed/26581717 http://dx.doi.org/10.1186/s12903-015-0118-3 |
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