4.6 Article

Synovial Fluid-Derived Extracellular Vesicles of Patients with Arthritides Contribute to Hippocampal Synaptic Dysfunctions and Increase with Mood Disorders Severity in Humans

Journal

CELLS
Volume 11, Issue 15, Pages -

Publisher

MDPI
DOI: 10.3390/cells11152276

Keywords

EVs; osteoarthritis; rheumatoid arthritis; synaptic transmission; neurons

Categories

Funding

  1. Italian Ministry of University and Research [5C22WM]
  2. SEED 2019-Bando Straordinario per Progetti Interdipartimentali, UNIMI
  3. University of Milan

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Arthritides is a group of diverse disorders that affect joints, including localized joint disorders and systemic autoimmune-driven diseases. Poor mental health is common among arthritides patients. Research has shown that extracellular vesicles derived from synovial fluid can affect neuronal function, and the concentration of synovial vesicles is associated with psychiatric symptoms in arthritides patients.
Arthritides are a highly heterogeneous group of disorders that include two major clinical entities, localized joint disorders such as osteoarthritis (OA) and systemic autoimmune-driven diseases such as rheumatoid arthritis (RA). Arthritides are characterized by chronic debilitating musculoskeletal conditions and systemic chronic inflammation. Poor mental health is also one of the most common comorbidities of arthritides. Depressive symptoms which are most prevalent, negatively impact patient global assessment diminishing the probability of achieving the target of clinical remission. Here, we investigated new insights into mechanisms that link different joint disorders to poor mental health, and to this issue, we explored the action of the synovial fluid-derived extracellular vesicles (EVs) on neuronal function. Our data show that the exposure of neurons to different concentrations of EVs derived from both RA and OA synovial fluids (RA-EVs and OA-EVs) leads to increased excitatory synaptic transmission but acts on specific modifications on excitatory or inhibitory synapses, as evidenced by electrophysiological and confocal experiments carried out in hippocampal cultures. The treatment of neurons with EVs membrane is also responsible for generating similar effects to those found with intact EVs suggesting that changes in neuronal ability arise upon EVs membrane molecules ' interactions with neurons. In humans with arthritides, we found that nearly half of patients (37.5%) showed clinically significant psychiatric symptoms (CGIs score >= 3), and at least mild anxiety (HAM-A >= 7) or depression (MADRS and HAM-D >= 7); interestingly, these individuals revealed an increased concentration of synovial EVs. In conclusion, our data showing opposite changes at the excitatory and inhibitory levels in neurons treated with OA- and RA-EVs, lay the scientific basis for personalized medicine in OA and RA patients, and identify EVs as new potential actionable biomarkers in patients with OA/RA with poor mental health.

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