Osteoarthritis is a morbid and costly condition affecting an increasingly larger segment of the population with a lack of effective treatment options. The pathophysiology of osteoarthritis is poorly understood; cell senescence is deemed to be contributory. Senescence of joint tissues particularly chondrocytes, synoviocytes (fibroblasts), and adipocytes is implicated in the pathogenesis through the production of senescence-associated proteins. Senescence-associated proteins are cytokines, matrix degradation enzymes, and chemokines that contribute to an inflammatory milieu which leads to the propagation of senescence. Senescence-modifying therapies include senolytics which eliminate senescent cells and senomorphics which inhibit the senescence-associated protein production of senescent cells. Treatments being investigated include novel agents as well as agents previously used in other conditions in rheumatology and other fields.
Keyphrases
- dna damage
- endothelial cells
- stress induced
- induced apoptosis
- rheumatoid arthritis
- oxidative stress
- gene expression
- single cell
- type diabetes
- knee osteoarthritis
- signaling pathway
- metabolic syndrome
- stem cells
- systemic lupus erythematosus
- bariatric surgery
- endoplasmic reticulum stress
- cell proliferation
- mass spectrometry
- extracellular matrix
- cell therapy
- single molecule
- juvenile idiopathic arthritis
- atomic force microscopy