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Identification of azurocidin as a potential periodontitis biomarker by a proteomic analysis of gingival crevicular fluid

BACKGROUND: The inflammatory disease periodontitis results in tooth loss and can even lead to diseases of the whole body if not treated. Gingival crevicular fluid (GCF) reflects the condition of the gingiva and contains proteins transuded from serum or cells at inflamed sites. In this study, we aime...

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Autores principales: Choi, Young-Jin, Heo, Sun-Hee, Lee, Jae-Mok, Cho, Je-Yoel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3162872/
https://www.ncbi.nlm.nih.gov/pubmed/21794177
http://dx.doi.org/10.1186/1477-5956-9-42
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author Choi, Young-Jin
Heo, Sun-Hee
Lee, Jae-Mok
Cho, Je-Yoel
author_facet Choi, Young-Jin
Heo, Sun-Hee
Lee, Jae-Mok
Cho, Je-Yoel
author_sort Choi, Young-Jin
collection PubMed
description BACKGROUND: The inflammatory disease periodontitis results in tooth loss and can even lead to diseases of the whole body if not treated. Gingival crevicular fluid (GCF) reflects the condition of the gingiva and contains proteins transuded from serum or cells at inflamed sites. In this study, we aimed to discover potential protein biomarkers for periodontitis in GCF proteome using LC-MS/MS. RESULTS: We identified 305 proteins from GCF of healthy individuals and periodontitis patients collected using a sterile gel loading tip by ESI-MS/MS coupled to nano-LC. Among these proteins, about 45 proteins were differentially expressed in the GCF proteome of moderate periodontitis patients when compared to the healthy individuals. We first identified azurocidin in the GCF, but not the saliva, as an upregulated protein in the periodontitis patients and verified its increased expression during periodontitis by ELISA using the GCF of the classified periodontitis patients compared to the healthy individuals. In addition, we found that azurocidin inhibited the differentiation of bone marrow-derived macrophages to osteoclasts. CONCLUSIONS: Our results show that GCF collection using a gel loading tip and subsequent LC-MS/MS analysis following 1D-PAGE proteomic separation are effective for the analysis of the GCF proteome. Our current results also suggest that azurocidin could be a potential biomarker candidate for the early detection of inflammatory periodontal destruction by gingivitis and some chronic periodontitis. Our data also suggest that azurocidin may have an inhibitory role in osteoclast differentiation and, thus, a protective role in alveolar bone loss during the early stages of periodontitis.
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spelling pubmed-31628722011-08-28 Identification of azurocidin as a potential periodontitis biomarker by a proteomic analysis of gingival crevicular fluid Choi, Young-Jin Heo, Sun-Hee Lee, Jae-Mok Cho, Je-Yoel Proteome Sci Research BACKGROUND: The inflammatory disease periodontitis results in tooth loss and can even lead to diseases of the whole body if not treated. Gingival crevicular fluid (GCF) reflects the condition of the gingiva and contains proteins transuded from serum or cells at inflamed sites. In this study, we aimed to discover potential protein biomarkers for periodontitis in GCF proteome using LC-MS/MS. RESULTS: We identified 305 proteins from GCF of healthy individuals and periodontitis patients collected using a sterile gel loading tip by ESI-MS/MS coupled to nano-LC. Among these proteins, about 45 proteins were differentially expressed in the GCF proteome of moderate periodontitis patients when compared to the healthy individuals. We first identified azurocidin in the GCF, but not the saliva, as an upregulated protein in the periodontitis patients and verified its increased expression during periodontitis by ELISA using the GCF of the classified periodontitis patients compared to the healthy individuals. In addition, we found that azurocidin inhibited the differentiation of bone marrow-derived macrophages to osteoclasts. CONCLUSIONS: Our results show that GCF collection using a gel loading tip and subsequent LC-MS/MS analysis following 1D-PAGE proteomic separation are effective for the analysis of the GCF proteome. Our current results also suggest that azurocidin could be a potential biomarker candidate for the early detection of inflammatory periodontal destruction by gingivitis and some chronic periodontitis. Our data also suggest that azurocidin may have an inhibitory role in osteoclast differentiation and, thus, a protective role in alveolar bone loss during the early stages of periodontitis. BioMed Central 2011-07-28 /pmc/articles/PMC3162872/ /pubmed/21794177 http://dx.doi.org/10.1186/1477-5956-9-42 Text en Copyright ©2011 Choi et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Choi, Young-Jin
Heo, Sun-Hee
Lee, Jae-Mok
Cho, Je-Yoel
Identification of azurocidin as a potential periodontitis biomarker by a proteomic analysis of gingival crevicular fluid
title Identification of azurocidin as a potential periodontitis biomarker by a proteomic analysis of gingival crevicular fluid
title_full Identification of azurocidin as a potential periodontitis biomarker by a proteomic analysis of gingival crevicular fluid
title_fullStr Identification of azurocidin as a potential periodontitis biomarker by a proteomic analysis of gingival crevicular fluid
title_full_unstemmed Identification of azurocidin as a potential periodontitis biomarker by a proteomic analysis of gingival crevicular fluid
title_short Identification of azurocidin as a potential periodontitis biomarker by a proteomic analysis of gingival crevicular fluid
title_sort identification of azurocidin as a potential periodontitis biomarker by a proteomic analysis of gingival crevicular fluid
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3162872/
https://www.ncbi.nlm.nih.gov/pubmed/21794177
http://dx.doi.org/10.1186/1477-5956-9-42
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