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MicroRNAs and immunity in periodontal health and disease
MicroRNAs (miRNAs) are critical regulators of the host immune and inflammatory response against bacterial pathogens. In the present review, we discuss target genes, target gene functions, the potential regulatory role of miRNAs in periodontal tissues, and the potential role of miRNAs as biomarkers a...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6080405/ https://www.ncbi.nlm.nih.gov/pubmed/30078842 http://dx.doi.org/10.1038/s41368-018-0025-y |
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author | Luan, Xianghong Zhou, Xiaofeng Naqvi, Afsar Francis, Marybeth Foyle, Deborah Nares, Salvador Diekwisch, Thomas G. H. |
author_facet | Luan, Xianghong Zhou, Xiaofeng Naqvi, Afsar Francis, Marybeth Foyle, Deborah Nares, Salvador Diekwisch, Thomas G. H. |
author_sort | Luan, Xianghong |
collection | PubMed |
description | MicroRNAs (miRNAs) are critical regulators of the host immune and inflammatory response against bacterial pathogens. In the present review, we discuss target genes, target gene functions, the potential regulatory role of miRNAs in periodontal tissues, and the potential role of miRNAs as biomarkers and therapeutics. In periodontal disease, miRNAs exert control over all aspects of innate and adaptive immunity, including the functions of neutrophils, macrophages, dendritic cells and T and B cells. Previous human studies have highlighted some key miRNAs that are dysregulated in periodontitis patients. In the present study, we mapped the major miRNAs that were altered in our reproducible periodontitis mouse model relative to control animals. The miRNAs that were upregulated as a result of periodontal disease in both human and mouse studies included miR-15a, miR-29b, miR-125a, miR-146a, miR-148/148a and miR-223, whereas miR-92 was downregulated. The association of individual miRNAs with unique aspects of periodontal disease and their stability in gingival crevicular fluid underscores their potential as markers for periodontal disease progression or healthy restitution. Moreover, miRNA therapeutics hold great promise for the future of periodontal therapy because of their ability to modulate the immune response to infection when applied in conjunction with synthetic antagomirs and/or relatively straightforward delivery strategies. |
format | Online Article Text |
id | pubmed-6080405 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-60804052018-08-08 MicroRNAs and immunity in periodontal health and disease Luan, Xianghong Zhou, Xiaofeng Naqvi, Afsar Francis, Marybeth Foyle, Deborah Nares, Salvador Diekwisch, Thomas G. H. Int J Oral Sci Review Article MicroRNAs (miRNAs) are critical regulators of the host immune and inflammatory response against bacterial pathogens. In the present review, we discuss target genes, target gene functions, the potential regulatory role of miRNAs in periodontal tissues, and the potential role of miRNAs as biomarkers and therapeutics. In periodontal disease, miRNAs exert control over all aspects of innate and adaptive immunity, including the functions of neutrophils, macrophages, dendritic cells and T and B cells. Previous human studies have highlighted some key miRNAs that are dysregulated in periodontitis patients. In the present study, we mapped the major miRNAs that were altered in our reproducible periodontitis mouse model relative to control animals. The miRNAs that were upregulated as a result of periodontal disease in both human and mouse studies included miR-15a, miR-29b, miR-125a, miR-146a, miR-148/148a and miR-223, whereas miR-92 was downregulated. The association of individual miRNAs with unique aspects of periodontal disease and their stability in gingival crevicular fluid underscores their potential as markers for periodontal disease progression or healthy restitution. Moreover, miRNA therapeutics hold great promise for the future of periodontal therapy because of their ability to modulate the immune response to infection when applied in conjunction with synthetic antagomirs and/or relatively straightforward delivery strategies. Nature Publishing Group UK 2018-08-06 /pmc/articles/PMC6080405/ /pubmed/30078842 http://dx.doi.org/10.1038/s41368-018-0025-y Text en © The Author(s) 2018 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Review Article Luan, Xianghong Zhou, Xiaofeng Naqvi, Afsar Francis, Marybeth Foyle, Deborah Nares, Salvador Diekwisch, Thomas G. H. MicroRNAs and immunity in periodontal health and disease |
title | MicroRNAs and immunity in periodontal health and disease |
title_full | MicroRNAs and immunity in periodontal health and disease |
title_fullStr | MicroRNAs and immunity in periodontal health and disease |
title_full_unstemmed | MicroRNAs and immunity in periodontal health and disease |
title_short | MicroRNAs and immunity in periodontal health and disease |
title_sort | micrornas and immunity in periodontal health and disease |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6080405/ https://www.ncbi.nlm.nih.gov/pubmed/30078842 http://dx.doi.org/10.1038/s41368-018-0025-y |
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