每2
下调和上调
DNA甲基化
基因敲除
昼夜节律
表观遗传学
基因沉默
生物
基因表达
甲基化
时钟
亚硫酸氢盐测序
生物钟
炎症
基因
分子生物学
遗传学
免疫学
内分泌学
作者
Ruifen Wei,Qianqian Chen,Qinxiang Zheng,Peter S. Reinach,Xiying Tan,Chengjie Pan,Wei Xu,Louis Tong,Wei Chen
标识
DOI:10.1080/09273948.2023.2205525
摘要
Purpose To explore whether circadian clock genes contribute to elicit inflammation in experimental dry eye (EDE).Methods RNA sequencing analyzed mRNA expression patterns in EDE model. RT-qPCR and/or Western blot determined the expression of inflammatory factors and circadian genes during EDE. MethylTarget™ assays determined the promoter methylation levels of Per genes in vivo. Per2 or Per3 knockdown assessed their effects on inflammatory factors in vitro.Results We utilized an intelligently controlled environmental system (ICES) to establish a mouse EDE model. The significant upregulated genes were enriched for circadian rhythms. Therein lied oscillatory and time-dependent upregulation of PER2 and PER3, as well as their promoter hypomethylation during EDE. Silencing PER2 or PER3 significantly decreased inflammatory factor expression and also reversed such increased inflammatory response in azacitidine (AZA) treatment in vitro model.Conclusions Our findings suggest that DNA methylation mediated the upregulation of PER2 and PER3, leading to inflammatory response in EDE.
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