Related Experiment Video
Updated: Jan 20, 2026

Detection of Functional Matrix Metalloproteinases by Zymography
Published on: November 8, 2010
The role of matrix metalloproteinases in osteoarthritis pathogenesis: An updated review
El-Sayed E Mehana1, Asmaa F Khafaga1, Samar S El-Blehi1
1Department of Pathology, Faculty of Veterinary Medicine, Alexandria University, Edfina 22758, Egypt.
Abstract:
Extensive degeneration of articular cartilage (AC) is a primary event in the pathogenesis of osteoarthritis (OA) and other types of joint and bone inflammation. OA results in the loss of joint function, usually accompanied by severe pain, and are the most common type of arthritis, affecting more than 10% of adults. The characteristic signs of OA are progressive cartilage destruction and, eventually, complete loss of chondrocytes. A key enzyme responsible for these degenerative changes in cartilage is matrix metalloproteinase-13 (MMP-13), which is thought to be a major contributor to the degenerative process occurring during OA pathogenesis. The aim of the present review is to shed light on the general role of MMPs, with special emphasis on MMP-13, in the induction of OA and the general basis of OA treatment. The pathogenic mechanism of this highly prevalent disease is not clear, and no effective disease-modifying treatment is currently available. Any updated information about OA treatment in human patients will also benefit companion animals such as horses and dogs, which also suffer from OA. Selective inhibition of MMP-13 seems to be an attractive therapeutic strategy.
More Related Videos
Related Concept Videos
The Extracellular Matrix
Role of Matrix Metalloproteases in Degradation of ECM
Review and Preview
Percentiles are a type of fractile that partition data into...
Review and Preview
Asthma: Pathogenesis and Management
Asthma is classified as allergic and non-allergic. Allergens such as dust mites, pollen, and pet dander trigger allergic asthma, while factors like cold air, intense emotions, or exercise can induce non-allergic asthma.
Cystic Fibrosis: Pathogenesis
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation,...

