Synovium-Synovial Fluid Axis in Osteoarthritis Pathology: A Key Regulator of the Cartilage Degradation Process

Genes (Basel). 2021 Jun 29;12(7):989. doi: 10.3390/genes12070989.

Abstract

Failure of conventional anti-inflammatory therapies in osteoarthritis (OA) underlines the insufficient knowledge about inflammatory mechanisms, patterns and their relationship with cartilage degradation. Considering non-linear nature of cartilage loss in OA, a better understanding of inflammatory milieu and MMP status at different stages of OA is required to design early-stage therapies or personalized disease management. For this, an investigation based on a synovium-synovial fluid (SF) axis was planned to study OA associated changes in synovium and SF along the progressive grades of OA. Gene expressions in synovial-biopsies from different grades OA patients (N = 26) revealed a peak of IL-1β, IL-15, PGE2 and NGF in early OA (Kellgren-Lawrence (KL) grade-I and II); the highest MMP levels were found in advanced stages (KL grade-III and IV). MMPs (MMP-1, 13, 2 and 9) abundance and FALGPA activity estimated in forty SFs of progressive grades showed the maximum protein levels and activity in KL grade-II and III. In an SF challenge test, SW982 and THP1 cells were treated with progressive grade SFs to study the dynamics of MMPs modulation in inflammatory microenvironment; the test yielded a result pattern, which matched with FALGPA and the protein-levels estimation. Inflammatory mediators in SFs served as steering factor for MMP up-regulation. A correlation-matrix of IL-1β and MMPs revealed expressional negative correlation.

Keywords: FALGPA; Kellgren–Lawrence radiographic grades; MMPs; inflammatory mediators; osteoarthritis; synovial-fluid; synovitis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cartilage / metabolism*
  • Cartilage / pathology
  • Dinoprostone / genetics
  • Dinoprostone / metabolism
  • Female
  • Humans
  • Interleukin-15 / genetics
  • Interleukin-15 / metabolism
  • Interleukin-1beta / genetics
  • Interleukin-1beta / metabolism
  • Male
  • Matrix Metalloproteinase 1 / genetics
  • Nerve Growth Factor / genetics
  • Nerve Growth Factor / metabolism
  • Oligopeptides / genetics
  • Oligopeptides / metabolism
  • Osteoarthritis / genetics*
  • Osteoarthritis / pathology
  • Osteoarthritis, Knee / genetics*
  • Osteoarthritis, Knee / metabolism
  • Synovial Fluid / metabolism
  • Synovial Membrane / metabolism*
  • Synovial Membrane / pathology

Substances

  • IL1B protein, human
  • Interleukin-15
  • Interleukin-1beta
  • Oligopeptides
  • 2-furanacryloyl-leucyl-glycyl-prolyl-alanine
  • Nerve Growth Factor
  • MMP1 protein, human
  • Matrix Metalloproteinase 1
  • Dinoprostone