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pmid:37965346

Immunological characterization of stroke-heart syndrome and identification of inflammatory therapeutic targets.

Junyi Zheng · Yilin Ma · Xukun Guo · Jialing Wu

Frontiers in immunology · 2023 doi:10.3389/fimmu.2023.1227104

Paper

complete

Experiment

complete

Data

partial

Analysis

partial

Execution

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Immunological characterization of stroke-heart syndrome and identification of inflammatory therapeutic targets.
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10.3389/fimmu.2023.1227104
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Junyi Zheng
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Yilin Ma
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Xukun Guo
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Jialing Wu
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Frontiers in immunology
year
2023
abstract
Acute cardiac dysfunction caused by stroke-heart syndrome (SHS) is the second leading cause of stroke-related death. The inflammatory response plays a significant role in the pathophysiological process of cardiac damage. However, the mechanisms underlying the brain-heart interaction are poorly understood. Therefore, we aimed to analysis the immunological characterization and identify inflammation therapeutic targets of SHS. We analyzed gene expression data of heart tissue 24 hours after induction of ischemia stoke by MCAO or sham surgery in a publicly available dataset (GSE102558) from Gene Expression Omnibus (GEO). Bioinformatics analysis revealed 138 differentially expressed genes (DEGs) in myocardium of MCAO-treated compared with sham-treated mice, among which, immune and inflammatory pathways were enriched. Analysis of the immune cells infiltration showed that the natural killer cell populations were significantly different between the two groups. We identified five DIREGs, Aplnr, Ccrl2, Cdkn1a, Irak2, and Serpine1 and found that their expression correlated with specific populations of infiltrating immune cells in the cardiac tissue. RT-qPCR and Western blot methods confirmed significant changes in the expression levels of Aplnr, Cdkn1a, Irak2, and Serpine1 after MCAO, which may serve as therapeutic targets to prevent cardiovascular complications after stroke.
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Applying the standard criteria of |log2fold change| ≥1 and adjusted P value < 0.05, we identified 138 DEGs, including 91 upregulated genes and 47 downregulated genes in MCAO-treated mice versus sham-treated mice
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Applying the standard criteria of |log2fold change| ≥1 and adjusted P value < 0.05, we identified 138 DEGs, including 91 upregulated genes and 47 downregulated genes in MCAO-treated mice versus sham-treated mice ( Figures 2A, B ).
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Applying the standard criteria of |log2fold change| ≥1 and adjusted P value < 0.05, we identified 138 DEGs, including 91 upregulated genes and 47 downregulated genes in MCAO-treated mice versus sham-treated mice ( Figures 2A, B ).
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Complete file
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