Identification of core cuprotosis-correlated biomarkers in abdominal aortic aneurysm immune microenvironment based on bioinformatics

被引:3
|
作者
Hu, Jiateng [1 ,2 ]
Xue, Song [3 ]
Xu, Zhijue [1 ,2 ]
Wu, Zhaoyu [1 ,2 ]
Xu, Xintong [1 ,2 ]
Wang, Xin [1 ,2 ]
Liu, Guang [1 ,2 ]
Lu, Xinwu [1 ,2 ]
Li, Bo [1 ,2 ]
Liu, Xiaobing [1 ,2 ]
机构
[1] Shanghai Jiao Tong Univ, Shanghai Peoples Hosp 9, Dept Vasc Surg, Sch Med, Shanghai, Peoples R China
[2] Shanghai Jiao Tong Univ, Vasc Ctr, Shanghai, Peoples R China
[3] Shanghai Jiao Tong Univ, Ruijin Hosp, Dept Orthoped, Sch Med, Shanghai, Peoples R China
来源
FRONTIERS IN IMMUNOLOGY | 2023年 / 14卷
基金
上海市自然科学基金; 中国国家自然科学基金;
关键词
Abdominal aortic aneurysm; Cuprotosis; FDX1; NLRP3; immune environment; VASCULAR SMOOTH-MUSCLE; COPPER TRANSPORTER; GENE-EXPRESSION; CELL-DEATH; FATTY-ACID; TRANSCRIPTS; ACTIVATION; PROTECTS; BINDING; DRIVES;
D O I
10.3389/fimmu.2023.1138126
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
BackgroundThe occurrence of abdominal aortic aneurysms (AAAs) is related to the disorder of immune microenvironment. Cuprotosis was reported to influence the immune microenvironment. The objective of this study is to identify cuprotosis-related genes involved in the pathogenesis and progression of AAA. MethodsDifferentially expressed lncRNAs (DElncRNAs) and mRNAs (DEmRNAs) in mouse were identified following AAA through high-throughput RNA sequencing. The enrichment analyses of pathway were selected through Gene Ontology (GO), Kyoto Encyclopedia of Genes and Genomes (KEGG). The validation of cuprotosis-related genes was conducted through immunofluorescence and western blot analyses. ResultsTotally, 27616 lncRNAs and 2189 mRNAs were observed to be differentially expressed (|Fold Change| >= 2 and q< 0.05) after AAA, including 10424 up-regulated and 17192 down-regulated lncRNAs, 1904 up-regulated and 285 down-regulated mRNAs. Gene ontology and KEGG pathway analysis showed that the DElncRNAs and DEmRNAs were implicated in many different biological processes and pathways. Furthermore, Cuprotosis-related genes (NLRP3, FDX1) were upregulated in the AAA samples compared with the normal one. ConclusionCuprotosis-related genes (NLRP3,FDX1) involved in AAA immune environment might be critical for providing new insight into identification of potential targets for AAA therapy.
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页数:12
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