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Autophagy-mediated regulation patterns contribute to the alterations of the immune microenvironment in periodontitis

机译:自噬介导的调节模式有助于牙周炎中免疫微环境的改变

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摘要

The relationship between autophagy and immunity has been thoroughly investigated. However, little is known about the role of autophagy in shaping the immune-microenvironment of periodontitis. Thus, we aim to explore the impact of autophagy on the immune-microenvironment of periodontitis. The expression distinctions of autophagy genes between healthy and periodontitis samples have been investigated. The connections between autophagy and immune characteristics including infiltrating immunocyte, immune reaction and human leukocyte antigen (HLA) gene were evaluated. The distinct autophagy-mediated expression patterns were identified and immune characteristics under distinct patterns were revealed. Autophagy phenotype-related genes were identified. 16 autophagy genes were dysregulated and a ten-autophagy classifier was constructed that can well distinguish periodontitis and healthy samples. Immune characteristics were closely related to autophagy: higher expression of EDEM1 positively relates to infiltrating activated B cell; NCKAP1 negatively relates to monocyte; CXCR4 enhances BCR Signaling Pathway and PEX3 decreases the activity of TNF Family Members Receptors; positive expression correlation of EDEM1-HLADOB and negative correlation of RAB11A-HLADOB were observed. Two distinct autophagy expression patterns were identified which demonstrated different immune characteristics. 4309 autophagy phenotype-related genes were identified, and 219 of them were related to immunity, whose biological functions were found to be involved in immunocyte regulations. Our study revealed the strong impact of autophagy on the immune-microenvironment of periodontitis and brought new insights into the understanding of the pathogenesis of periodontitis.
机译:已彻底调查自噬和免疫关系之间的关系。然而,关于自噬在牙周炎的免疫微环境中的作用很少熟知。因此,我们的目标是探讨自噬对牙周炎的免疫微环境的影响。已经研究了健康和牙周炎样本之间自噬基因的表达。评价包括渗透免疫细胞,免疫反应和人白细胞抗原(HLA)基因的自噬和免疫特性之间的连接。鉴定了不同的自噬介导的表达模式,并揭示了不同图案下的免疫特征。鉴定了自噬表型相关基因。 16型自噬基因被抑制,构建了10自血管分类器,可以很好地区分牙周炎和健康样品。免疫特征与自噬密切相关:Edem1的高表达呈正相关,涉及浸润活性B细胞; nckap1对单核细胞呈负相关; CXCR4增强BCR信号通路,PEX3降低TNF家族成员受体的活性;观察到Rab11a-Hladob的正面表达相关性和Rab11a-Hladob的负相关性。鉴定了两种不同的自噬表达模式,其显示出不同的免疫特征。鉴定了4309型自噬表型相关基因,其中219个与免疫有关,其生物学功能被发现参与免疫细胞法规。我们的研究揭示了自噬对牙周炎免疫微环境的强烈影响,并为牙周炎发病机制带来了新的见解。

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