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Mitochondrial pathology in osteoarthritic chondrocytes.

Abstract
Osteoarthritis (OA) is a chronic degenerative disease leading to aberrance of cartilage structures with unclear or multifactorial mechanisms. Recently, a great portion of research endeavor to explore the molecular mechanisms of OA in focusing on the mitochondrial pathology. Mitochondrial respiratory chain (MRC) produces reactive oxygen species (ROS), which in turn impair mtDNA integrity and link to cartilage degradation in OA. The fine-tuning between ROS and antioxidant within chondrocytes ensures cartilage homeostasis. With disturbance from pro-inflammatory cytokines, oxidative stress synergistically instigates cellular signaling and exacerbates mitochondrial pathology, which may affect several pathways implicated in OA cartilage degradation, including oxidative stress, increase of cytokine-induced chondrocytes inflammation and matrix catabolism, aging and senescence, obesity-related pathology, and cartilage matrix calcification. Unveiling the molecular mechanisms of mitochondrial function in OA pathogenesis and progression is essential for providing relevant therapeutic targets. These suggest that efficient protection and improvement of mitochondrial activity can be a therapeutic alternative for OA patients.
AuthorsLonghuo Wu, Haiqing Liu, Linfu Li, Hai Liu, Qilai Cheng, Hongliang Li, Hao Huang
JournalCurrent drug targets (Curr Drug Targets) Vol. 15 Issue 7 Pg. 710-9 ( 2014) ISSN: 1873-5592 [Electronic] United Arab Emirates
PMID24745822 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Review)
Chemical References
  • Antioxidants
  • Cytokines
  • Reactive Oxygen Species
  • Calcium
Topics
  • Aging (metabolism, pathology)
  • Antioxidants (metabolism)
  • Calcium (metabolism)
  • Cartilage (immunology, metabolism, pathology)
  • Chondrocytes (immunology, metabolism, pathology)
  • Cytokines (immunology)
  • Humans
  • Mitochondria (immunology, metabolism, pathology)
  • Obesity (complications, metabolism, pathology)
  • Osteoarthritis (etiology, metabolism, pathology)
  • Oxidative Stress
  • Reactive Oxygen Species (metabolism)

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