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Proteomic Analysis of a Noninvasive Human Model of Acute Inflammation and Its Resolution: The Twenty-one Day Gingivitis Model
[Image: see text] The 21-day experimental gingivitis model, an established noninvasive model of inflammation in response to increasing bacterial accumulation in humans, is designed to enable the study of both the induction and resolution of inflammation. Here, we have analyzed gingival crevicular fl...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2950674/ https://www.ncbi.nlm.nih.gov/pubmed/20662485 http://dx.doi.org/10.1021/pr100446f |
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author | Grant, Melissa M. Creese, Andrew J. Barr, Gordon Ling, Martin R. Scott, Ann E. Matthews, John B. Griffiths, Helen R. Cooper, Helen J. Chapple, Iain L. C. |
author_facet | Grant, Melissa M. Creese, Andrew J. Barr, Gordon Ling, Martin R. Scott, Ann E. Matthews, John B. Griffiths, Helen R. Cooper, Helen J. Chapple, Iain L. C. |
author_sort | Grant, Melissa M. |
collection | PubMed |
description | [Image: see text] The 21-day experimental gingivitis model, an established noninvasive model of inflammation in response to increasing bacterial accumulation in humans, is designed to enable the study of both the induction and resolution of inflammation. Here, we have analyzed gingival crevicular fluid, an oral fluid comprising a serum transudate and tissue exudates, by LC−MS/MS using Fourier transform ion cyclotron resonance mass spectrometry and iTRAQ isobaric mass tags, to establish meta-proteomic profiles of inflammation-induced changes in proteins in healthy young volunteers. Across the course of experimentally induced gingivitis, we identified 16 bacterial and 186 human proteins. Although abundances of the bacterial proteins identified did not vary temporally, Fusobacterium outer membrane proteins were detected. Fusobacterium species have previously been associated with periodontal health or disease. The human proteins identified spanned a wide range of compartments (both extracellular and intracellular) and functions, including serum proteins, proteins displaying antibacterial properties, and proteins with functions associated with cellular transcription, DNA binding, the cytoskeleton, cell adhesion, and cilia. PolySNAP3 clustering software was used in a multilayered analytical approach. Clusters of proteins that associated with changes to the clinical parameters included neuronal and synapse associated proteins. |
format | Text |
id | pubmed-2950674 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-29506742010-10-06 Proteomic Analysis of a Noninvasive Human Model of Acute Inflammation and Its Resolution: The Twenty-one Day Gingivitis Model Grant, Melissa M. Creese, Andrew J. Barr, Gordon Ling, Martin R. Scott, Ann E. Matthews, John B. Griffiths, Helen R. Cooper, Helen J. Chapple, Iain L. C. J Proteome Res [Image: see text] The 21-day experimental gingivitis model, an established noninvasive model of inflammation in response to increasing bacterial accumulation in humans, is designed to enable the study of both the induction and resolution of inflammation. Here, we have analyzed gingival crevicular fluid, an oral fluid comprising a serum transudate and tissue exudates, by LC−MS/MS using Fourier transform ion cyclotron resonance mass spectrometry and iTRAQ isobaric mass tags, to establish meta-proteomic profiles of inflammation-induced changes in proteins in healthy young volunteers. Across the course of experimentally induced gingivitis, we identified 16 bacterial and 186 human proteins. Although abundances of the bacterial proteins identified did not vary temporally, Fusobacterium outer membrane proteins were detected. Fusobacterium species have previously been associated with periodontal health or disease. The human proteins identified spanned a wide range of compartments (both extracellular and intracellular) and functions, including serum proteins, proteins displaying antibacterial properties, and proteins with functions associated with cellular transcription, DNA binding, the cytoskeleton, cell adhesion, and cilia. PolySNAP3 clustering software was used in a multilayered analytical approach. Clusters of proteins that associated with changes to the clinical parameters included neuronal and synapse associated proteins. American Chemical Society 2010-07-27 2010-09-03 /pmc/articles/PMC2950674/ /pubmed/20662485 http://dx.doi.org/10.1021/pr100446f Text en Copyright © 2010 American Chemical Society http://pubs.acs.org This is an open-access article distributed under the ACS AuthorChoice Terms & Conditions. Any use of this article, must conform to the terms of that license which are available at http://pubs.acs.org. |
spellingShingle | Grant, Melissa M. Creese, Andrew J. Barr, Gordon Ling, Martin R. Scott, Ann E. Matthews, John B. Griffiths, Helen R. Cooper, Helen J. Chapple, Iain L. C. Proteomic Analysis of a Noninvasive Human Model of Acute Inflammation and Its Resolution: The Twenty-one Day Gingivitis Model |
title | Proteomic Analysis of a Noninvasive Human Model of Acute Inflammation and Its Resolution: The Twenty-one Day Gingivitis Model |
title_full | Proteomic Analysis of a Noninvasive Human Model of Acute Inflammation and Its Resolution: The Twenty-one Day Gingivitis Model |
title_fullStr | Proteomic Analysis of a Noninvasive Human Model of Acute Inflammation and Its Resolution: The Twenty-one Day Gingivitis Model |
title_full_unstemmed | Proteomic Analysis of a Noninvasive Human Model of Acute Inflammation and Its Resolution: The Twenty-one Day Gingivitis Model |
title_short | Proteomic Analysis of a Noninvasive Human Model of Acute Inflammation and Its Resolution: The Twenty-one Day Gingivitis Model |
title_sort | proteomic analysis of a noninvasive human model of acute inflammation and its resolution: the twenty-one day gingivitis model |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2950674/ https://www.ncbi.nlm.nih.gov/pubmed/20662485 http://dx.doi.org/10.1021/pr100446f |
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