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Transcriptomic phases of periodontitis lesions using the nonhuman primate model

We used a nonhuman primate model of ligature-induced periodontitis to identify patterns of gingival transcriptomic after changes demarcating phases of periodontitis lesions (initiation, progression, resolution). A total of 18 adult Macaca mulatta (12–22 years) had ligatures placed (premolar, 1st mol...

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Autores principales: Ebersole, Jeffrey L., Nagarajan, Radhakrishnan, Kirakodu, Sreenatha, Gonzalez, Octavio A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8085193/
https://www.ncbi.nlm.nih.gov/pubmed/33927312
http://dx.doi.org/10.1038/s41598-021-88803-6
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author Ebersole, Jeffrey L.
Nagarajan, Radhakrishnan
Kirakodu, Sreenatha
Gonzalez, Octavio A.
author_facet Ebersole, Jeffrey L.
Nagarajan, Radhakrishnan
Kirakodu, Sreenatha
Gonzalez, Octavio A.
author_sort Ebersole, Jeffrey L.
collection PubMed
description We used a nonhuman primate model of ligature-induced periodontitis to identify patterns of gingival transcriptomic after changes demarcating phases of periodontitis lesions (initiation, progression, resolution). A total of 18 adult Macaca mulatta (12–22 years) had ligatures placed (premolar, 1st molar teeth) in all 4 quadrants. Gingival tissue samples were obtained (baseline, 2 weeks, 1 and 3 months during periodontitis and at 5 months resolution). Gene expression was analyzed by microarray [Rhesus Gene 1.0 ST Array (Affymetrix)]. Compared to baseline, a large array of genes were significantly altered at initiation (n = 6049), early progression (n = 4893), and late progression (n = 5078) of disease, with the preponderance being up-regulated. Additionally, 1918 genes were altered in expression with disease resolution, skewed towards down-regulation. Assessment of the genes demonstrated specific profiles of epithelial, bone/connective tissue, apoptosis/autophagy, metabolism, regulatory, immune, and inflammatory responses that were related to health, stages of disease, and tissues with resolved lesions. Unique transcriptomic profiles occured during the kinetics of the periodontitis lesion exacerbation and remission. We delineated phase specific gene expression profiles of the disease lesion. Detection of these gene products in gingival crevicular fluid samples from human disease may contribute to a better understanding of the biological dynamics of the disease to improve patient management.
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spelling pubmed-80851932021-05-03 Transcriptomic phases of periodontitis lesions using the nonhuman primate model Ebersole, Jeffrey L. Nagarajan, Radhakrishnan Kirakodu, Sreenatha Gonzalez, Octavio A. Sci Rep Article We used a nonhuman primate model of ligature-induced periodontitis to identify patterns of gingival transcriptomic after changes demarcating phases of periodontitis lesions (initiation, progression, resolution). A total of 18 adult Macaca mulatta (12–22 years) had ligatures placed (premolar, 1st molar teeth) in all 4 quadrants. Gingival tissue samples were obtained (baseline, 2 weeks, 1 and 3 months during periodontitis and at 5 months resolution). Gene expression was analyzed by microarray [Rhesus Gene 1.0 ST Array (Affymetrix)]. Compared to baseline, a large array of genes were significantly altered at initiation (n = 6049), early progression (n = 4893), and late progression (n = 5078) of disease, with the preponderance being up-regulated. Additionally, 1918 genes were altered in expression with disease resolution, skewed towards down-regulation. Assessment of the genes demonstrated specific profiles of epithelial, bone/connective tissue, apoptosis/autophagy, metabolism, regulatory, immune, and inflammatory responses that were related to health, stages of disease, and tissues with resolved lesions. Unique transcriptomic profiles occured during the kinetics of the periodontitis lesion exacerbation and remission. We delineated phase specific gene expression profiles of the disease lesion. Detection of these gene products in gingival crevicular fluid samples from human disease may contribute to a better understanding of the biological dynamics of the disease to improve patient management. Nature Publishing Group UK 2021-04-29 /pmc/articles/PMC8085193/ /pubmed/33927312 http://dx.doi.org/10.1038/s41598-021-88803-6 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Ebersole, Jeffrey L.
Nagarajan, Radhakrishnan
Kirakodu, Sreenatha
Gonzalez, Octavio A.
Transcriptomic phases of periodontitis lesions using the nonhuman primate model
title Transcriptomic phases of periodontitis lesions using the nonhuman primate model
title_full Transcriptomic phases of periodontitis lesions using the nonhuman primate model
title_fullStr Transcriptomic phases of periodontitis lesions using the nonhuman primate model
title_full_unstemmed Transcriptomic phases of periodontitis lesions using the nonhuman primate model
title_short Transcriptomic phases of periodontitis lesions using the nonhuman primate model
title_sort transcriptomic phases of periodontitis lesions using the nonhuman primate model
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8085193/
https://www.ncbi.nlm.nih.gov/pubmed/33927312
http://dx.doi.org/10.1038/s41598-021-88803-6
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