Exosomal amyloid A and lymphatic vessel endothelial hyaluronic acid receptor-1 proteins are associated with disease activity in rheumatoid arthritis

• Published in: Arthritis research & therapy Vol. 19; no. 1; p. 119
• Main Authors: Yoo, Jihyung, Lee, Sang Kwang, Lim, Mikyung, Sheen, Donghyuk, Choi, Eun-Hye, Kim, Soon Ae
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 31-05-2017; BioMed Central; BMC
• Subjects: Adult; Aged; Amyloid A; Arthritis; Arthritis, Rheumatoid - metabolism; Arthritis, Rheumatoid - pathology; Biological markers; Biomarker; Biomarkers; Biomarkers - analysis; Blood; Cancer; Chromatography; Cytokines; Development and progression; Disease; Exosomes; Exosomes - metabolism; Female; Health risk assessment; Humans; LYVE-1; Mass spectrometry; MicroRNA; Middle Aged; Pathogenesis; Proteins; Proteomics; Rheumatoid arthritis; Scientific imaging; Serum Amyloid A Protein - analysis; Serum Amyloid A Protein - metabolism; Tumor necrosis factor-TNF; Vesicular Transport Proteins - analysis; Vesicular Transport Proteins - metabolism; Biomarker; Exosomes; Rheumatoid arthritis; LYVE-1; Amyloid A
• DOI: 10.1186/s13075-017-1334-9
• EISSN: 1478-6362
• ISSN: 1478-6362; 1478-6354

Exosomes are thought to play an important role in exchanging information between cells. The proteins and lipids in exosomes play roles in mediating inflammatory and autoimmune diseases. The aim of this study was to identify exosomal candidate proteins that are related to other inflammatory parameters in rheumatoid arthritis (RA).
The study population consisted of 60 patients with RA: 30 in the clinical remission (CR) group with a Disease Activity Score in 28 joints based on erythrocyte sedimentation rate (DAS28-ESR) ≤2.6 and 30 in the non-clinical remission (non-CR) group with a DAS28-ESR >2.6. Preparation of exosomes from patient serum samples was performed with the ExoQuick kit, and protein identification/quantification was performed using tandem mass tag labeling/mass spectrometry and an enzyme-linked immunosorbent assay. Comparisons between groups were made using Student's t test or the Mann-Whitney U test, as appropriate. Spearman's correlation coefficients (ρ) were calculated.
We identified six candidate proteins. Exosomal levels of amyloid A (AA) and lymphatic vessel endothelial hyaluronic acid receptor-1 (LYVE-1) differed between the CR and non-CR groups. Both serum and exosomal AA levels were higher in the non-CR group than in the CR group (p = 0.001). Significant positive correlations were found between exosomal AA and C-reactive protein (CRP) as well as between serum AA and CRP (ρ = 0.614, p = 0.001, and ρ = 0.624, p = 0.001, respectively). Although serum levels of LYVE-1 did not differ between the non-CR and CR groups, exosomal levels of LYVE-1 were lower in the non-CR group than in the CR group (p = 0.01). We identified positive correlations between serum/exosomal LYVE-1 and CRP only in the non-CR group (serum ρ = 0.376, p = 0.04; exosome ρ = 0.545, p = 0.002).
Exosomal LYVE-1 shows potential for use as an additional marker of disease activity in patients with RA, and exosomes may carry other useful markers for RA.