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Author Spotlight: Isolation and Culture of Primary Synovial Macrophages and Fibroblasts from Murine Arthritis Tissue
Published on: February 24, 2023
Identification of Candidate Genes Related to Synovial Macrophages in Rheumatoid Arthritis by Bioinformatics Analysis
Jia Xu1, Ming-Ying Zhang2, Wei Jiao1
1First Clinical Medical School, Guangzhou University of Chinese Medicine, Guangzhou, 510405, Guangdong, People's Republic of China.
Objective:
Rheumatoid arthritis (RA) is one of the most prevalent inflammatory arthritis worldwide. However, the genes and pathways associated with macrophages from synovial fluids in RA patients still remain unclear. This study aims to screen and verify differentially expressed genes (DEGs) related to identifying candidate genes related to synovial macrophages in rheumatoid arthritis by bioinformatics analysis.
Methods:
We searched the Gene Expression Omnibus (GEO) database, and GSE97779 and GSE10500 with synovial macrophages expression profiling from multiple RA microarray dataset were selected to conduct a systematic analysis. GSE97779 included nine macrophage samples from synovial fluids of RA patients and five macrophage samples from primary human blood of HC. GSE10500 included five macrophage samples from synovial fluids of RA patients and three macrophage samples from primary human blood of HC. Functional annotation of DEGs was performed, including Gene Ontology (GO) analysis and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analysis. Protein-protein interaction (PPI) network of DEGs was established using the STRING database. CytoHubba was used to identify hub genes. MCODE was used to determine gene clusters in the interactive network.
Results:
There were 2638 DEGs (1425 upregulated genes and 1213 downregulated ones) and 889 DEGs (438 upregulated genes and 451 downregulated ones) selected from GSE97779 and GSE10500, respectively. Venn diagrams showed that 173 genes were upregulated and 106 downregulated in both two datasets. The top 10 hub genes, including FN1, VEGFA, HGF, SERPINA1, MMP9, PPBP, CD44, FPR2, IGF1, and ITGAM, were identified using the PPI network.
Conclusion:
This study provides new insights for the potential biomarkers and the relevant molecular mechanisms in RA patients. Our findings suggest that the 10 candidate genes might be used in diagnosis, prognosis, and therapy of RA in the future. However, further studies are required to confirm the expression of these genes in synovial macrophages in RA and control specimen.
Insights
This study identifies 10 key genes in synovial macrophages of rheumatoid arthritis (RA) patients. These genes may serve as potential biomarkers for RA diagnosis, prognosis, and therapy.
Area of Science:
- Immunology
- Genetics
- Bioinformatics
Background:
- Rheumatoid arthritis (RA) is a widespread inflammatory condition.
- The specific genes and pathways in synovial fluid macrophages of RA patients are not fully understood.
Purpose of the Study:
- To identify and validate differentially expressed genes (DEGs) in synovial macrophages from RA patients.
- To uncover candidate genes and molecular mechanisms associated with RA pathogenesis.
Main Methods:
- Utilized Gene Expression Omnibus (GEO) datasets (GSE97779, GSE10500) for microarray analysis of RA synovial macrophages.
- Performed Gene Ontology (GO) and KEGG pathway enrichment analysis on DEGs.
- Constructed a protein-protein interaction (PPI) network to identify hub genes using STRING and CytoHubba.
Main Results:
- Identified 2638 DEGs in GSE97779 and 889 DEGs in GSE10500.
- Found 173 upregulated and 106 downregulated genes common to both datasets.
- Identified 10 top hub genes, including FN1, VEGFA, HGF, and MMP9, via PPI network analysis.
Conclusions:
- The study highlights potential biomarkers and molecular mechanisms in RA.
- The 10 identified candidate genes warrant further investigation for RA diagnosis, prognosis, and therapeutic applications.
- Further research is needed to confirm gene expression in RA synovial macrophages.
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