Department of Oral Biochemistry, Kagoshima University Graduate School of Medical and Dental Sciences, Japan.
Department of Periodontology, Kagoshima University Graduate School of Medical and Dental Sciences, Japan.
J Oral Biosci. 2022 Jun;64(2):229-236. doi: 10.1016/j.job.2022.04.004. Epub 2022 Apr 25.
The oral cavity is one of the main entry sites for SARS-CoV-2. Gingival keratinocytes express transmembrane serine protease 2 (TMPRSS2), responsible for priming the SARS-CoV-2 spike protein. We investigated whether periodontitis increased the expression of TMPRSS2.
To investigate gene expression in periodontitis, we analyzed the expression of specific genes from (1) the Gene Expression Omnibus (GEO) dataset of 247 human gingival tissues and (2) an experimentally-induced periodontitis mouse model. Human gingival tissues with or without periodontitis were immunohistochemically stained using an anti-TMPRSS2 antibody. Analysis of the TMPRSS2 promoter was performed using a ChIP-Atlas dataset. TMPRSS2 expression was detected in cultured human keratinocytes using quantitative reverse transcription (qRT)-PCR and Western blot analysis.
GEO dataset analysis and an experimentally-induced periodontitis model revealed increased expression of TMPRSS2 in periodontitis gingiva. The keratinocyte cell membrane in periodontitis gingiva was strongly immunohistochemically stained for TMPRSS2. Using ChIP-Atlas and GEO datasets, we screened for transcription factors that bind to the TMPRSS2 promoter region. We found one candidate, estrogen receptor 1 (ESR1), highly expressed in periodontitis gingiva. Analysis of the GEO dataset revealed a correlation between ESR1 and TMPRSS2 expression in gingival tissues. An ESR1 ligand induced TMPRSS2 expression in cultured keratinocytes.
Periodontitis increases TMPRSS2 expression in the cell membrane of gingival keratinocytes.
口腔是 SARS-CoV-2 的主要进入部位之一。牙龈角质形成细胞表达跨膜丝氨酸蛋白酶 2(TMPRSS2),负责对 SARS-CoV-2 刺突蛋白进行初步处理。我们研究了牙周炎是否会增加 TMPRSS2 的表达。
为了研究牙周炎中的基因表达,我们分析了(1)来自 247 个人类牙龈组织的基因表达综合数据库(GEO)数据集和(2)实验性诱导牙周炎的小鼠模型中的特定基因的表达。使用抗 TMPRSS2 抗体对有或没有牙周炎的人类牙龈组织进行免疫组织化学染色。使用 ChIP-Atlas 数据集分析 TMPRSS2 启动子。使用定量逆转录(qRT)-PCR 和 Western blot 分析检测培养的人角质形成细胞中的 TMPRSS2 表达。
GEO 数据集分析和实验性诱导牙周炎模型显示,牙周炎牙龈中 TMPRSS2 的表达增加。牙周炎牙龈的角质形成细胞膜强烈免疫组织化学染色 TMPRSS2。使用 ChIP-Atlas 和 GEO 数据集,我们筛选与 TMPRSS2 启动子区域结合的转录因子。我们发现了一个候选物,即雌激素受体 1(ESR1),在牙周炎牙龈中高度表达。GEO 数据集的分析显示,在牙龈组织中,ESR1 与 TMPRSS2 的表达之间存在相关性。ESR1 配体诱导培养的角质形成细胞中 TMPRSS2 的表达。
牙周炎增加了牙龈角质形成细胞中细胞膜上的 TMPRSS2 表达。