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Differentiation of Functional Osteoclasts from Human Peripheral Blood CD14+ Monocytes
Published on: January 27, 2023
CD14 and CSF1R as developmental molecular targets for the induction of osteoarthritis
Meiliang Zheng1, Zheng Li1, Yingfa Feng2
1Department of Orthopedics, The Second Central Hospital of Baoding No. 57 Fanyang Zhong Road, Zhuozhou 072750, Hebei, China.
Objective:
Osteoarthritis (OA) is a non-inflammatory degenerative joint disease that mainly involves articular cartilage damage and involves the whole joint tissue. However, the relationship between CD14 and CSF1R and osteoarthritis remains unclear. The aim of this study was to explore the important role of CD14 and CSF1R in osteoarthritis and provide a new direction for its prevention and treatment.
Method:
The osteoarthritis datasets GSE46750 and GSE82107 were downloaded from gene expression omnibus (GEO) database generated by GPL10558 and GPL570. R package limma was used to screen differentially expressed genes (DEDs). Weighted gene co-expression network analysis (WGCNA) was performed. The construction and analysis of a protein-protein interaction (PPI) network, functional enrichment analysis, gene set enrichment analysis (GSEA), and comparative toxicogenomics database (CTD) analysis were performed. TargetScan screened miRNAs that regulated central DEGs.
Results:
687 DEGs were identified. According to gene ontology (GO), they were mainly concentrated in inflammatory response, IL-17 signaling pathway, rheumatoid arthritis, exercise, and regulation of response to external stimuli. The enrichment items are similar to the GO Kyoto Encyclopedia of Gene and Genome (KEGG) enrichment items of DEGs. These were mainly concentrated in exercise, inflammatory response, defense response, collagen containing extracellular matrix, and receptor regulator activity. In an enrichment project of Metascape, GO had inflammatory response, SARS-CoV-2 signal pathway network map, PIDIL8CXCR1 pathway, regulation of bone remodeling and endochondral ossification. 20 core genes were obtained by PPI network construction and analysis. Gene expression heat map showed that core genes (C1QC, CSF1R, CD14, TYROBP, HLA-DRA, C1QB, FCER1G, S100A9, HCLS1, WAS, BTK, TREM1) were highly expressed in osteoarthritis synovial tissues and were low in normal synovial tissues. CTD analysis showed that twelve genes (C1QC, CSF1R, CD14, TYROBP, HLA-DRA, C1QB, FCER1G, S100A9, HCLS1, WAS, BTK, TREM1) were found to be associated with inflammation, necrosis, gout, acute myeloid leukemia and thrombocytopenia.
Conclusion:
CD14 and CSF1R are highly expressed in osteoarthritis and may be therapeutic targets for osteoarthritis.
Insights
This study reveals that CD14 and CSF1R are highly expressed in osteoarthritis, suggesting they are potential therapeutic targets for this degenerative joint disease.
Area of Science:
- * Molecular biology and bioinformatics.
- * Genomics and transcriptomics.
- * Osteoarthritis research.
Background:
- * Osteoarthritis (OA) is a degenerative joint disease primarily affecting articular cartilage.
- * The roles of CD14 and CSF1R in OA pathogenesis are not well understood.
- * Clarifying these roles could offer new therapeutic strategies for OA.
Purpose of the Study:
- * To investigate the involvement of CD14 and CSF1R in osteoarthritis.
- * To identify key genes and pathways associated with OA.
- * To explore potential therapeutic targets for OA prevention and treatment.
Main Methods:
- * Analysis of osteoarthritis datasets (GSE46750, GSE82107) from the Gene Expression Omnibus (GEO) database.
- * Differential gene expression analysis using the R package limma.
- * Weighted gene co-expression network analysis (WGCNA), protein-protein interaction (PPI) network construction, and functional enrichment analyses (GO, KEGG, Metascape).
- * Comparative Toxicogenomics Database (CTD) analysis and miRNA target prediction.
Main Results:
- * Identified 687 differentially expressed genes (DEGs) primarily enriched in inflammatory response and signaling pathways.
- * Discovered 20 core genes through PPI network analysis, with CD14 and CSF1R showing high expression in OA synovial tissues.
- * CTD analysis linked twelve core genes, including CD14 and CSF1R, to inflammation and other related conditions.
Conclusions:
- * CD14 and CSF1R are significantly upregulated in osteoarthritis.
- * These genes represent promising therapeutic targets for osteoarthritis.
- * Further research into CD14 and CSF1R could lead to novel OA treatments.
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