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Detection of Exosomal PD-L1 RNA in Saliva of Patients With Periodontitis

Periodontitis is the most prevalent inflammatory disease of the periodontium, and is related to oral and systemic health. Exosomes are emerging as non-invasive biomarker for liquid biopsy. We here evaluated the levels of programmed death-ligand 1 (PD-L1) mRNA in salivary exosomes from patients with...

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Autores principales: Yu, Jialiang, Lin, Yusheng, Xiong, Xiao, Li, Kai, Yao, Zhimeng, Dong, Hongmei, Jiang, Zuojie, Yu, Dan, Yeung, Sai-Ching Jim, Zhang, Hao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6426748/
https://www.ncbi.nlm.nih.gov/pubmed/30923536
http://dx.doi.org/10.3389/fgene.2019.00202
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author Yu, Jialiang
Lin, Yusheng
Xiong, Xiao
Li, Kai
Yao, Zhimeng
Dong, Hongmei
Jiang, Zuojie
Yu, Dan
Yeung, Sai-Ching Jim
Zhang, Hao
author_facet Yu, Jialiang
Lin, Yusheng
Xiong, Xiao
Li, Kai
Yao, Zhimeng
Dong, Hongmei
Jiang, Zuojie
Yu, Dan
Yeung, Sai-Ching Jim
Zhang, Hao
author_sort Yu, Jialiang
collection PubMed
description Periodontitis is the most prevalent inflammatory disease of the periodontium, and is related to oral and systemic health. Exosomes are emerging as non-invasive biomarker for liquid biopsy. We here evaluated the levels of programmed death-ligand 1 (PD-L1) mRNA in salivary exosomes from patients with periodontitis and non-periodontitis controls. The purposes of this study were to establish a procedure for isolation and detection of mRNA in exosomes from saliva of periodontitis patients, to characterize the level of salivary exosomal PD-L1, and to illustrate its clinical relevance. Bioinformatics analysis suggested that periodontitis was associated with an inflammation gene expression signature, that PD-L1 expression positively correlated with inflammation in periodontitis based on gene set enrichment analysis (GSEA) and that PD-L1 expression was remarkably elevated in periodontitis patients versus control subjects. Exosomal RNAs were successfully isolated from saliva of 61 patients and 30 controls and were subjected to qRT-PCR. Levels of PD-L1 mRNA in salivary exosomes were higher in periodontitis patients than controls (P < 0.01). Salivary exosomal PD-L1 mRNA showed significant difference between the stages of periodontitis. In summary, the protocols for isolating and detecting exosomal RNA from saliva of periodontitis patients were, for the first time, characterized. The current study suggests that assay of exosomes-based PD-L1 mRNA in saliva has potential to distinguish periodontitis from the healthy, and the levels correlate with the severity/stage of periodontitis.
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spelling pubmed-64267482019-03-28 Detection of Exosomal PD-L1 RNA in Saliva of Patients With Periodontitis Yu, Jialiang Lin, Yusheng Xiong, Xiao Li, Kai Yao, Zhimeng Dong, Hongmei Jiang, Zuojie Yu, Dan Yeung, Sai-Ching Jim Zhang, Hao Front Genet Genetics Periodontitis is the most prevalent inflammatory disease of the periodontium, and is related to oral and systemic health. Exosomes are emerging as non-invasive biomarker for liquid biopsy. We here evaluated the levels of programmed death-ligand 1 (PD-L1) mRNA in salivary exosomes from patients with periodontitis and non-periodontitis controls. The purposes of this study were to establish a procedure for isolation and detection of mRNA in exosomes from saliva of periodontitis patients, to characterize the level of salivary exosomal PD-L1, and to illustrate its clinical relevance. Bioinformatics analysis suggested that periodontitis was associated with an inflammation gene expression signature, that PD-L1 expression positively correlated with inflammation in periodontitis based on gene set enrichment analysis (GSEA) and that PD-L1 expression was remarkably elevated in periodontitis patients versus control subjects. Exosomal RNAs were successfully isolated from saliva of 61 patients and 30 controls and were subjected to qRT-PCR. Levels of PD-L1 mRNA in salivary exosomes were higher in periodontitis patients than controls (P < 0.01). Salivary exosomal PD-L1 mRNA showed significant difference between the stages of periodontitis. In summary, the protocols for isolating and detecting exosomal RNA from saliva of periodontitis patients were, for the first time, characterized. The current study suggests that assay of exosomes-based PD-L1 mRNA in saliva has potential to distinguish periodontitis from the healthy, and the levels correlate with the severity/stage of periodontitis. Frontiers Media S.A. 2019-03-14 /pmc/articles/PMC6426748/ /pubmed/30923536 http://dx.doi.org/10.3389/fgene.2019.00202 Text en Copyright © 2019 Yu, Lin, Xiong, Li, Yao, Dong, Jiang, Yu, Yeung and Zhang. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Yu, Jialiang
Lin, Yusheng
Xiong, Xiao
Li, Kai
Yao, Zhimeng
Dong, Hongmei
Jiang, Zuojie
Yu, Dan
Yeung, Sai-Ching Jim
Zhang, Hao
Detection of Exosomal PD-L1 RNA in Saliva of Patients With Periodontitis
title Detection of Exosomal PD-L1 RNA in Saliva of Patients With Periodontitis
title_full Detection of Exosomal PD-L1 RNA in Saliva of Patients With Periodontitis
title_fullStr Detection of Exosomal PD-L1 RNA in Saliva of Patients With Periodontitis
title_full_unstemmed Detection of Exosomal PD-L1 RNA in Saliva of Patients With Periodontitis
title_short Detection of Exosomal PD-L1 RNA in Saliva of Patients With Periodontitis
title_sort detection of exosomal pd-l1 rna in saliva of patients with periodontitis
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6426748/
https://www.ncbi.nlm.nih.gov/pubmed/30923536
http://dx.doi.org/10.3389/fgene.2019.00202
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