Matrix metalloproteases and tissue inhibitors of metalloproteinases in medial plica and pannus-like tissue contribute to knee osteoarthritis progression

PLoS One. 2013 Nov 4;8(11):e79662. doi: 10.1371/journal.pone.0079662. eCollection 2013.

Abstract

Osteoarthritis (OA) is characterized by degradation of the cartilage matrix, leading to pathologic changes in the joints. However, the pathogenic effects of synovial tissue inflammation on OA knees are not clear. To investigate whether the inflammation caused by the medial plica is involved in the pathogenesis of osteoarthritis, we examined the expression of matrix metalloproteinases (MMPs), tissue inhibitors of metalloproteinases (TIMPs), interleukin (IL)-1β, and tumor necrosis factor (TNF)-α in the medial plica and pannus-like tissue in the knees of patients with medial compartment OA who underwent either arthroscopic medial release (stage II; 15 knee joints from 15 patients) or total knee replacement (stage IV; 18 knee joints from 18 patients). MMP-2, MMP-3, MMP-9, IL-1β, and TNF-α mRNA and protein levels measured, respectively, by quantitative real-time PCR and Quantibody human MMP arrays, were highly expressed in extracts of medial plica and pannus-like tissue from stage IV knee joints. Immunohistochemical staining also demonstrated high expression of MMP-2, MMP-3, and MMP-9 in plica and pannus-like tissue of stage IV OA knees and not in normal cartilage. Some TIMP/MMP ratios decreased significantly in both medial plica and pannus-like tissue as disease progressed from stage II to stage IV. Furthermore, the migration of cells from the pannus-like tissue was enhanced by IL-1β, while plica cell migration was enhanced by TNF-α. The results suggest that medial plica and pannus-like tissue may be involved in the process of cartilage degradation in medial compartment OA of the knee.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Movement / drug effects
  • Disease Progression*
  • Extracellular Matrix / drug effects
  • Extracellular Matrix / metabolism
  • Gene Expression Regulation, Enzymologic / drug effects
  • Humans
  • Interleukin-1beta / pharmacology
  • Joint Capsule / drug effects
  • Joint Capsule / metabolism*
  • Knee Joint / metabolism*
  • Knee Joint / pathology
  • Matrix Metalloproteinases / genetics
  • Matrix Metalloproteinases / metabolism*
  • Osteoarthritis, Knee / enzymology
  • Osteoarthritis, Knee / genetics
  • Osteoarthritis, Knee / metabolism*
  • Osteoarthritis, Knee / pathology*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Tissue Inhibitor of Metalloproteinases / genetics
  • Tissue Inhibitor of Metalloproteinases / metabolism*
  • Tumor Necrosis Factor-alpha / pharmacology

Substances

  • Interleukin-1beta
  • RNA, Messenger
  • Tissue Inhibitor of Metalloproteinases
  • Tumor Necrosis Factor-alpha
  • Matrix Metalloproteinases

Grants and funding

Supported by the Tzu-Chi Dalin General Hospital, Chiayi, Taiwan (S.-R. Lyu) and by a grant from the National Science Council, Taiwan (NSC100-2320-B-010-013) to H.-S. Wang, and a grant from the Ministry of Education, Taiwan, Aim for the Top University Plan (H.-S. Wang). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.