Comprehensive analysis of serum exosome-derived lncRNAs and mRNAs from patients with rheumatoid arthritis

• Published in: Arthritis research & therapy 2023-10, Vol.25 (1), p.1-201, Article 201
• Main Authors: Xue, Li, Wang, Biao, Li, Xueyi, Zhu, Jianhong, Wang, Wei, Huang, Fang, Wang, Xiaofei, Jin, Yaofeng, Xiong, Chaoliang, Tao, Li, Xu, Ke, Wang, Jing, Guo, Ying, Xu, Jing, Yang, Xin, Wang, Na, Gao, Ning, Wang, Yan, Li, Ke, Li, Ming, Geng, Yan
• Format: Article
• Language: English
• Subjects: Analysis; Arthritis; Autoimmune diseases; Biomarkers; Diagnosis; Genes; Genetic aspects; lncRNA; Messenger RNA; MicroRNAs; mRNAs; Proteins; Rheumatoid arthritis; Rheumatology; RNA; RNA-sequencing; Serum exosomes
• ISSN: 1478-6362; 1478-6354; 1478-6362
• DOI: 10.1186/s13075-023-03174-9

Background Serum exosomes play important roles in intercellular communication and are promising biomarkers of several autoimmune diseases. However, the biological functions and potential clinical importance of long non-coding RNAs (lncRNAs) and mRNAs from serum exosomes in rheumatoid arthritis (RA) have not yet been studied. Methods Serum exosomal lncRNAs and mRNAs were isolated from patients with RA and osteoarthritis (OA) and healthy controls. The differentially expressed lncRNAs (DE-lncRNAs) and mRNA profiles in the serum exosomes of patients with RA were analysed using high-throughput sequencing, and their functions were predicted using Gene Ontologyenrichment, Kyoto Encyclopedia of Genes and Genomes pathway, and gene set enrichment analysis. We constructed a DE-lncRNA-mRNA network and a protein-protein interaction network of differentially expressed mRNAs (DE-mRNAs) in RA using the Cytoscape software. The expression of several candidate a DE-lncRNAs and DE-mRNAs in the serum of patients with RA, patients with OA, and healthy controls was confirmed by qRT-PCR. We assessed the diagnostic ability of DE-lncRNAs and DE-mRNAs in patients with RA using receiver operating characteristic analysis. Furthermore, we analysed the characteristics of immune cell infiltration in RA by digital cytometry using the CIBERSORT algorithm and determined the correlation between immune cells and several DE-lncRNAs or DE-mRNAs in RA. Results The profiles of serum exosomal lncRNAs and mRNAs in patients with RA were different from those in healthy controls and patients with OA. The functions of both DE-lncRNAs and DE-mRNAs in RA are associated with the immune response and cellular metabolic processes. The RT-PCR results show that NONHSAT193357.1, CCL5, and MPIG6B were downregulated in patients with RA. The combination of three DE-mRNAs, CCL5, MPIG6B, and PFKP, had an area under the curve of 0.845 for differentiating RA from OA. Digital cytometry using the CIBERSORT algorithm showed that the neutrophil counts were higher in patients with RA than those in healthy controls and patients with OA. Conclusions These findings help to elucidate the role of serum exosomal lncRNAs and mRNAs in the specific mechanisms underlying RA. Keywords: Rheumatoid arthritis, Serum exosomes, lncRNA, mRNAs, RNA-sequencing