Wang Liwen, Wu Di, Ma Ziwei, Song Di, Sun Yuanqiang, Pan Xuefeng, Zhang Junhui
Department of Ophthalmology, Huzhou Central Hospital, Huzhou, China.
The First People's Hospital of Huzhou, The First Affiliated Hospital of Huzhou Teacher College, Huzhou, China.
PLoS One. 2025 Sep 25;20(9):e0331281. doi: 10.1371/journal.pone.0331281. eCollection 2025.
Clinically, ocular application of corticosteroids is common.But it always result in higher Intraocular pressure (IOP).The potential molecular events are not clearly explained.It was reported that immune cells may cause higher IOP.This study aimed to identify the central gene and immune-related pathways in ocular tissue treated with corticosteroids.
The GSE124114 and GSE37474 was obtained from Gene Expression Omnibus database. Hub gene were acquired by differential expression analysis (DEGs).Weighted gene co-expression network analysis (WGCNA) identified hub gene modules associated with elevated intraocular pressure (IOP).CIBERSORT was utilized to evaluate the presence of immune cells in ocular tissue.R (version 3.6.1) was used to carry out enrichment analysis for DEGs.The STRING database constructed the protein-protein interaction network for differentially expressed genes (DEGs).The expression of hub genes was validated using the combined datasets GSE6298 and GSE65240. ROC analysis was conducted for clinical diagnosis in patients with elevated IOP.
30 DEGs were recognized. Gene ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analyses revealed that these DEGs were mainly associated with the positive regulation of cytokine production and pathways related to phenylalanine metabolism.Two hub modules were enriched in the rheumatoid arthritis and AGE-RAGE signaling pathways associated with diabetic complications. Analysis of the protein-protein interaction (PPI) network identified TSC22D3 and FKBP5 as related hub genes. Analysis of immune infiltration indicated a significant association between TSC22D3 and Macrophages M0 (R = 0.75, p = 0.018).The result of ROC for FKBP5 was 0.913.Consolidated GSE6298, GSE65240 database verified that FKBP5 gene was associated with IOP.In the results of qPCR, relative mRNA level of FKBP5 were incread.
Two key genes (TSC22D3, FKBP5) are involved in the molecular mechanisms in corticosteroids-induce higher IOP. TSC22D3 was probably associated with the immune response in ocular tissue. FKBP5 may be a potential novel diagnostic gene for higher IOP.
临床上,眼部应用皮质类固醇很常见。但它总是导致眼内压(IOP)升高。潜在的分子事件尚未得到明确解释。据报道,免疫细胞可能导致眼内压升高。本研究旨在确定用皮质类固醇处理的眼组织中的核心基因和免疫相关途径。
从基因表达综合数据库获取GSE124114和GSE37474。通过差异表达分析(DEG)获得枢纽基因。加权基因共表达网络分析(WGCNA)确定与眼内压升高相关的枢纽基因模块。利用CIBERSORT评估眼组织中免疫细胞的存在情况。使用R(版本3.6.1)对DEG进行富集分析。STRING数据库构建差异表达基因(DEG)的蛋白质-蛋白质相互作用网络。使用合并数据集GSE6298和GSE65240验证枢纽基因的表达。对眼内压升高患者进行ROC分析以用于临床诊断。
识别出30个DEG。基因本体(GO)和京都基因与基因组百科全书(KEGG)通路分析表明,这些DEG主要与细胞因子产生的正调控以及与苯丙氨酸代谢相关的通路有关。两个枢纽模块在与糖尿病并发症相关的类风湿关节炎和AGE-RAGE信号通路中富集。蛋白质-蛋白质相互作用(PPI)网络分析确定TSC22D3和FKBP5为相关枢纽基因。免疫浸润分析表明TSC22D3与巨噬细胞M0之间存在显著关联(R = 0.75,p = 0.018)。FKBP5的ROC结果为0.913。合并的GSE6298、GSE65240数据库验证FKBP5基因与眼内压相关。在qPCR结果中,FKBP5的相对mRNA水平升高。
两个关键基因(TSC22D3、FKBP5)参与皮质类固醇诱导眼内压升高的分子机制。TSC22D3可能与眼组织中的免疫反应有关。FKBP5可能是眼内压升高的潜在新型诊断基因。