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加权基因共表达网络分析(WGCNA)探讨人牙龈成纤维细胞中对生物膜反应的基因和免疫浸润分析。

Weighted gene co-expression network analysis (WGCNA) to explore genes responsive to biofilm and immune infiltration analysis in human gingival fibroblasts cells.

机构信息

Department of Stomatology, Affiliated Yueqing Hospital, Wenzhou Medical University; Institute of Stomatology, School and Hospital of Stomatology, Wenzhou Medical University, Wenzhou, Zhejiang, China.

Department of Prosthodontics, School and Hospital of Stomatology, Wenzhou Medical University, Wenzhou, Zhejiang, China.

出版信息

Bioengineered. 2021 Dec;12(1):1054-1065. doi: 10.1080/21655979.2021.1902697.

Abstract

The correlation between oral bacteria and dental implants failure has been reported. However, the effect and mechanism of bacteria during dental implants is unclear. In this study, we explored key genes and candidate gene clusters in human gingival fibroblasts (HGF) cells in response to biofilm through weighted gene co-expression network analysis (WGCNA) and differential genes analysis using gene expression matrix, GSE134481, downloaded from the Gene Expression Omnibus (GEO) database. We obtained 325 genes in the module significantly associated with infection and 113 differentially expressed genes (DEGs) in the biofilm; 62 DEGs indicated significant correlation with injury. Multiple immune pathways, such as the tumor necrosis factor (TNF) signaling pathway, were considerably enriched. We obtained a candidate genes cluster containing 12 genes - , and ; we observed 5 candidate hub genes associated with infection - , and . The fraction of macrophage M0 cells was significantly increased in biofilm treatment compared with control; expression of and was significantly positively correlated with macrophage M0 cells. Our findings present a fierce inflammation changes in the transcript level of HGF in response to .

摘要

已经有报道称口腔细菌与牙种植体失败之间存在相关性。然而,细菌在牙种植体中的作用和机制尚不清楚。在这项研究中,我们通过加权基因共表达网络分析(WGCNA)和使用基因表达矩阵(GSE134481)进行差异基因分析,从基因表达综合数据库(GEO)中下载,探索了人牙龈成纤维细胞(HGF)对生物膜反应的关键基因和候选基因簇。我们获得了与感染显著相关的模块中的 325 个基因和生物膜中的 113 个差异表达基因(DEGs);62 个 DEGs 表明与损伤有显著相关性。大量免疫途径,如肿瘤坏死因子(TNF)信号通路,得到了极大的丰富。我们获得了一个包含 12 个基因的候选基因簇-、和;我们观察到与感染相关的 5 个候选枢纽基因-、和。与对照组相比,生物膜处理组中 M0 巨噬细胞的比例明显增加;和的表达与 M0 巨噬细胞呈显著正相关。我们的研究结果表明,HGF 在转录水平上对生物膜的反应存在强烈的炎症变化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e817/8806260/34fa767adfb7/KBIE_A_1902697_UF0001_OC.jpg

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