Hyaluronic Acid and Large Extracellular Vesicles (EVs) in Synovial Fluid and Plasma of Patients With End-Stage Arthritis: Positive Association of EVs to Joint Pain

Author:

Mustonen Anne-Mari12,Capra Janne3,Oikari Sanna1,Säisänen Laura45,Karttunen Lauri6,Julkunen Petro45,Lehenkari Petri78,Joukainen Antti9,Jaroma Antti10,Paakkonen Tommi1,Kääriäinen Tommi9,Kröger Heikki1011,Nieminen Petteri1ORCID

Affiliation:

1. Institute of Biomedicine, School of Medicine, Faculty of Health Sciences, University of Eastern Finland, Kuopio, Finland

2. Department of Environmental and Biological Sciences, Faculty of Science, Forestry and Technology, University of Eastern Finland, Joensuu, Finland

3. Cell and Tissue Imaging Unit, Institute of Biomedicine, School of Medicine, Faculty of Health Sciences, University of Eastern Finland, Kuopio, Finland

4. Department of Clinical Neurophysiology, Kuopio University Hospital, Kuopio, Finland

5. Department of Technical Physics, Faculty of Science, Forestry and Technology, University of Eastern Finland, Kuopio, Finland

6. Department of Rehabilitation, Kuopio University Hospital, Kuopio, Finland

7. Cancer and Translational Medicine Research Unit, Faculty of Medicine, University of Oulu, Oulu, Finland

8. Department of Surgery and Medical Research Center, Oulu University Hospital, Oulu, Finland

9. Pihlajalinna, Kuopio, Finland

10. Department of Orthopaedics, Traumatology and Hand Surgery, Kuopio University Hospital, Kuopio, Finland

11. Kuopio Musculoskeletal Research Unit, University of Eastern Finland, Kuopio, Finland

Abstract

Objective Hyaluronic acid (HA) in synovial fluid (SF) contributes to boundary lubrication with altered levels in osteoarthritis (OA) and rheumatoid arthritis (RA). SF extracellular vesicles (EVs) may participate in arthritis by affecting inflammation and cartilage degradation. It remains unknown whether HA and EVs display joint-specific alterations in arthritic SFs. Design We investigated the numbers and characteristics of HA-particles and large EVs in SF from knees and shoulders of 8 OA and 8 RA patients and 8 trauma controls, and in plasma from 10 healthy controls and 11 knee OA patients. The plasma and SF HA concentrations were determined with a sandwich-type enzyme-linked sorbent assay, and EVs and HA-particles were characterized from plasma and unprocessed and centrifuged SFs with confocal microscopy. The data were compared according to diagnosis, location, and preanalytical processing. Results The main findings were: (1) OA and RA SFs can be distinguished from trauma joints based on the distinctive profiles of HA-particles and large EVs, (2) there are differences in the SF HA and EV characteristics between shoulder and knee joints that could reflect their dissimilar mobility, weight-bearing, and shock absorption properties, (3) EV counts in SF and plasma can positively associate with pain parameters independent of age and body adiposity, and (4) low-speed centrifugation causes alterations in the features of HA-particles and EVs, complicating their examination in the original state. Conclusions Arthritis and anatomical location can affect the characteristics of HA-particles and large EVs that may have potential as biomarkers and effectors in joint degradation and pain.

Funder

Research Council of Finland

Publisher

SAGE Publications

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