4.5 Article

Characterization of hyaluronan-coated extracellular vesicles in synovial fluid of patients with osteoarthritis and rheumatoid arthritis

Journal

BMC MUSCULOSKELETAL DISORDERS
Volume 22, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s12891-021-04115-w

Keywords

Extracellular vesicles; Hyaluronan; Osteoarthritis; Rheumatoid arthritis; Synovial fluid

Funding

  1. Jane and Aatos Erkko Foundation
  2. Academy of Finland [276426, 284520, 312519, 322429]
  3. Biocenter Kuopio
  4. Biocenter Finland
  5. Academy of Finland (AKA) [284520, 312519, 322429, 312519, 284520, 322429] Funding Source: Academy of Finland (AKA)

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The study successfully developed a method for quantifying EV, HA particles, and HA-EV in human knee joint SF using CLSM and image analysis. The results showed that the fluorescence intensities of EV and HA particles were lower in RA patients compared to the control group and OA group, indicating potential implications for diagnosis and therapy in rheumatoid arthritis SF.
Background Hyaluronic acid (HA) is the major extracellular matrix glycosaminoglycan with a reduced synovial fluid (SF) concentration in arthropathies. Cell-derived extracellular vesicles (EV) have also been proposed to contribute to pathogenesis in joint diseases. It has recently been shown that human SF contains HA-coated EV (HA-EV), but their concentration and function in joint pathologies remain unknown. Methods The aim of the present study was to develop an applicable method based on confocal laser scanning microscopy (CLSM) and image analysis for the quantification of EV, HA-particles, and HA-EV in the SF of the human knee joint. Samples were collected during total knee replacement surgery from patients with end-stage rheumatoid arthritis (RA, n = 8) and osteoarthritis (OA, n = 8), or during diagnostic/therapeutic arthroscopy unrelated to OA/RA (control, n = 7). To characterize and quantify EV, HA-particles, and HA-EV, SF was double-stained with plasma membrane and HA probes and visualized by CLSM. Comparisons between the patient groups were performed with the Kruskal-Wallis analysis of variance. Results The size distribution of EV and HA-particles was mostly similar in the study groups. Approximately 66% of EV fluorescence was co-localized with HA verifying that a significant proportion of EV carry HA. The study groups were clearly separated by the discriminant analysis based on the CLSM data. The intensities of EV and HA-particle fluorescences were lower in the RA than in the control and OA groups. Conclusions CLSM analysis offers a useful tool to assess HA-EV in SF samples. The altered EV and HA intensities in the RA SF could have possible implications for diagnostics and therapy.

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