首页> 外文期刊>Journal of immunology research. >Crosstalk between RNA-Binding Proteins and Immune Microenvironment Revealed Two RBP Regulatory Patterns with Distinct Immunophenotypes in Periodontitis
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Crosstalk between RNA-Binding Proteins and Immune Microenvironment Revealed Two RBP Regulatory Patterns with Distinct Immunophenotypes in Periodontitis

机译:RNA结合蛋白和免疫微环境之间的串扰揭示了牙周炎中具有不同免疫蛋白酶的两个RBP调节模式

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Periodontitis is an inflammatory disease whose pathogenesis is closely related with immunology. RNA-binding proteins (RBPs) were found to play crucial roles in immunity. Therefore, we aimed to investigate the potential impact of RBPs in the immune microenvironment in periodontitis. The differential expressions of RBPs in periodontitis and healthy samples were determined and were used to construct an RBP-based classifier for periodontitis using logistic regression. The correlations between RBPs and immune characteristics were investigated by the Spearman correlation. Unsupervised clustering was conducted to identify the RBP regulatory patterns. RBP-related genes were identified by WGCNA, while biological distinctions were revealed by GSVA and GO. 24 dysregulated RBPs were identified, from which a 12-RBP classifier was established to distinguish periodontitis with AUC of 0.942. Close protein-protein interactions and expression correlations were observed especially between SPATS2 and ISG20. ISG20 and ESRP1 were found to be highly correlated with immunocyte infiltration, immune signaling activation, and HLA expressions in periodontitis. Two distinct RBP regulatory patterns were identified with different immune and other biological characteristics in periodontitis. Our findings indicate a significant impact of RBPs in shaping the immune microenvironment in periodontitis, which might bring new insights into the understanding of immune mechanisms in the pathogenesis of periodontitis.
机译:牙周炎是一种炎症性疾病,其发病机制与免疫学密切相关。发现RNA结合蛋白(RBPS)在免疫中起重要作用。因此,我们旨在调查RBP在牙周炎中免疫微环境中的潜在影响。确定RBPS在牙周炎和健康样品中的差异表达,并用于使用Logistic回归构建用于牙周炎的RBP基分类器。通过Spearman相关研究了RBP和免疫特征之间的相关性。进行无监督的聚类以确定RBP监管模式。通过WGCNA鉴定RBP相关基因,而GSVA并揭示生物学区分。鉴定了24个疑难解失措的RBP,从中建立了12-RBP分类剂以区分牙周炎的0.942。特别观察到密切的蛋白质 - 蛋白质相互作用和表达相关性,尤其是在SPATS2和ISG20之间。发现ISG20和ESRP1与牙周炎中的免疫细胞浸润,免疫信号激活和HLA表达高度相关。用不同的免疫和其他生物学特征鉴定出两种不同的RBP调节模式。我们的研究结果表明RBP在牙周炎中塑造免疫微环境的显着影响,这可能会对牙周炎发病机制的理解带来新的见解。

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