Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2006 Sep;16(9):1543-47.

[Destruction of articular cartilage]

[Article in Japanese]
Affiliations
  • PMID: 16951481
Review

[Destruction of articular cartilage]

[Article in Japanese]
Tatsuya Koike. Clin Calcium. 2006 Sep.

Abstract

Proinflammatory cytokines, such as interleukin-1 (IL-1) and tumour necrosis factor alpha (TNF alpha), have been implicated in the dysregulation of bone and cartilage remodelling characteristic of rheumatoid arthritis (RA) and/or osteoarthritis (OA). These cytokines increase production of factors that stimulate cartilage matrix degradation such as metalloproteinases. The matrix metalloproteinases (MMPs), the a disintegrin and metalloproteinase (ADAMs) and a disintegrin and metalloproteinase with thrombospondin repeats (ADAM-TSs) are secreted by many cell types including chondrocytes and cells in the synovium under the influences of cytokines. The role of the matalloproteinases in the irreversible degradation of articular cartilage has been extensively documented. We have already succeeded in halting the progression of joint damage by RA using anti-TNF therapy. The precise understanding of the roles of metalloproteinases should provide new therapeutic strategies for OA.

PubMed Disclaimer

Similar articles

MeSH terms

LinkOut - more resources