Injurious Loading of Articular Cartilage Compromises Chondrocyte Respiratory Function

Arthritis Rheumatol. 2016 Mar;68(3):662-71. doi: 10.1002/art.39460.

Abstract

Objective: To determine whether repeatedly overloading healthy cartilage disrupts mitochondrial function in a manner similar to that associated with osteoarthritis (OA) pathogenesis.

Methods: We exposed normal articular cartilage on bovine osteochondral explants to 1 day or 7 consecutive days of cyclic axial compression (0.25 MPa or 1.0 MPa at 0.5 Hz for 3 hours) and evaluated the effects on chondrocyte viability, ATP concentration, reactive oxygen species (ROS) production, indicators of oxidative stress, respiration, and mitochondrial membrane potential.

Results: Neither 0.25 MPa nor 1.0 MPa of cyclic compression caused extensive chondrocyte death, macroscopic tissue damage, or overt changes in stress-strain behavior. After 1 day of loading, differences in respiratory activities between the 0.25 MPa and 1.0 MPa groups were minimal; however, after 7 days of loading, respiratory activity and ATP levels were suppressed in the 1.0 MPa group relative to the 0.25 MPa group, an effect prevented by pretreatment with 10 mM N-acetylcysteine. These changes were accompanied by increased proton leakage and decreased mitochondrial membrane potential, as well as by increased ROS formation, as indicated by dihydroethidium staining and glutathione oxidation.

Conclusion: Repeated overloading leads to chondrocyte oxidant-dependent mitochondrial dysfunction. This mitochondrial dysfunction may contribute to destabilization of cartilage during various stages of OA in distinct ways by disrupting chondrocyte anabolic responses to mechanical stimuli.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Adenosine Triphosphate / analysis
  • Animals
  • Cartilage, Articular / physiopathology*
  • Cattle
  • Cell Respiration / physiology*
  • Cell Survival / physiology
  • Cells, Cultured
  • Chondrocytes / metabolism
  • Chondrocytes / physiology*
  • Ethidium / analogs & derivatives
  • Ethidium / metabolism
  • Glutathione / metabolism
  • Glutathione Disulfide / metabolism
  • In Vitro Techniques
  • Membrane Potential, Mitochondrial / physiology
  • Mitochondria / physiology
  • Osteoarthritis / etiology
  • Oxidation-Reduction
  • Oxidative Stress / physiology
  • Reactive Oxygen Species / metabolism

Substances

  • Reactive Oxygen Species
  • dihydroethidium
  • Adenosine Triphosphate
  • Ethidium
  • Glutathione
  • Glutathione Disulfide