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Transcriptome analysis of ankylosed primary molars with infraocclusion
Primary molar ankylosis with infraocclusion can retard dental arch development and cause dental asymmetry. Despite its widespread prevalence, little is known about its molecular etiology and pathogenesis. To address this, RNA sequencing was used to generate transcriptomes of furcal bone from infraoc...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7033215/ https://www.ncbi.nlm.nih.gov/pubmed/32080164 http://dx.doi.org/10.1038/s41368-019-0070-1 |
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author | Tong, Annie Chow, Yuh-Lit Xu, Katie Hardiman, Rita Schneider, Paul Tan, Seong-Seng |
author_facet | Tong, Annie Chow, Yuh-Lit Xu, Katie Hardiman, Rita Schneider, Paul Tan, Seong-Seng |
author_sort | Tong, Annie |
collection | PubMed |
description | Primary molar ankylosis with infraocclusion can retard dental arch development and cause dental asymmetry. Despite its widespread prevalence, little is known about its molecular etiology and pathogenesis. To address this, RNA sequencing was used to generate transcriptomes of furcal bone from infraoccluded (n = 7) and non-infraoccluded (n = 9) primary second molars, all without succeeding biscuspids. Of the 18 529 expressed genes, 432 (2.3%) genes were differentially expressed between the two groups (false discovery rate < 0.05). Hierarchical clustering and principal component analysis showed clear separation in gene expression between infraoccluded and non-infraoccluded samples. Pathway analyses indicated that molar ankylosis is associated with the expression of genes consistent with the cellular inflammatory response and epithelial cell turnover. Independent validation using six expressed genes by immunohistochemical analysis demonstrated that the corresponding proteins are strongly expressed in the developing molar tooth germ, in particular the dental follicle and inner enamel epithelium. The descendants of these structures include the periodontal ligament, cementum, bone and epithelial rests of Malassez; tissues that are central to the ankylotic process. We therefore propose that ankylosis involves an increased inflammatory response associated with disruptions to the developmental remnants of the dental follicle and epithelial rests of Malassez. |
format | Online Article Text |
id | pubmed-7033215 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-70332152020-03-04 Transcriptome analysis of ankylosed primary molars with infraocclusion Tong, Annie Chow, Yuh-Lit Xu, Katie Hardiman, Rita Schneider, Paul Tan, Seong-Seng Int J Oral Sci Article Primary molar ankylosis with infraocclusion can retard dental arch development and cause dental asymmetry. Despite its widespread prevalence, little is known about its molecular etiology and pathogenesis. To address this, RNA sequencing was used to generate transcriptomes of furcal bone from infraoccluded (n = 7) and non-infraoccluded (n = 9) primary second molars, all without succeeding biscuspids. Of the 18 529 expressed genes, 432 (2.3%) genes were differentially expressed between the two groups (false discovery rate < 0.05). Hierarchical clustering and principal component analysis showed clear separation in gene expression between infraoccluded and non-infraoccluded samples. Pathway analyses indicated that molar ankylosis is associated with the expression of genes consistent with the cellular inflammatory response and epithelial cell turnover. Independent validation using six expressed genes by immunohistochemical analysis demonstrated that the corresponding proteins are strongly expressed in the developing molar tooth germ, in particular the dental follicle and inner enamel epithelium. The descendants of these structures include the periodontal ligament, cementum, bone and epithelial rests of Malassez; tissues that are central to the ankylotic process. We therefore propose that ankylosis involves an increased inflammatory response associated with disruptions to the developmental remnants of the dental follicle and epithelial rests of Malassez. Nature Publishing Group UK 2020-02-21 /pmc/articles/PMC7033215/ /pubmed/32080164 http://dx.doi.org/10.1038/s41368-019-0070-1 Text en © The Author(s) 2020 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 | Article Tong, Annie Chow, Yuh-Lit Xu, Katie Hardiman, Rita Schneider, Paul Tan, Seong-Seng Transcriptome analysis of ankylosed primary molars with infraocclusion |
title | Transcriptome analysis of ankylosed primary molars with infraocclusion |
title_full | Transcriptome analysis of ankylosed primary molars with infraocclusion |
title_fullStr | Transcriptome analysis of ankylosed primary molars with infraocclusion |
title_full_unstemmed | Transcriptome analysis of ankylosed primary molars with infraocclusion |
title_short | Transcriptome analysis of ankylosed primary molars with infraocclusion |
title_sort | transcriptome analysis of ankylosed primary molars with infraocclusion |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7033215/ https://www.ncbi.nlm.nih.gov/pubmed/32080164 http://dx.doi.org/10.1038/s41368-019-0070-1 |
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