AI Article Synopsis

  • The study investigates how oxygen levels affect the behavior of chondrocytes in osteoarthritis (OA) and macroscopically normal (MN) cartilage.
  • Chondrocytes from OA cartilage produce more cartilage-degrading enzymes and rely on glycolysis for energy, especially under different oxygen conditions.
  • Higher oxygen levels in OA cartilage may contribute to cartilage damage, highlighting the importance of oxygen in understanding OA progression.

Article Abstract

Chondrocyte phenotype and energy metabolism are altered in osteoarthritis (OA). However, most studies characterising the change in human chondrocyte behaviour in OA have been conducted in supraphysiological oxygen concentrations. The purpose of this study was to compare phenotype and energy metabolism in chondrocytes from macroscopically normal (MN) and OA cartilage maintained in 18.9% (standard tissue culture), 6% (equivalent to superficial zone of cartilage in vivo) or 1% oxygen (equivalent to deep zone of cartilage in vivo). MMP13 production was higher in chondrocytes from OA compared to MN cartilage in hyperoxia and physoxia but not hypoxia. Hypoxia promoted SOX9, COL2A1 and ACAN protein expression in chondrocytes from MN but not OA cartilage. OA chondrocytes used higher levels of glycolysis regardless of oxygen availability. These results show that differences in phenotype and energy metabolism between chondrocytes from OA and MN cartilage differ depending on oxygen availability. OA chondrocytes show elevated synthesis of cartilage-catabolising enzymes and chondrocytes from MN cartilage show reduced cartilage anabolism in oxygenated conditions. This is relevant as a recent study has shown that oxygen levels are elevated in OA cartilage in vivo. Our findings may indicate that this elevated cartilage oxygenation may promote cartilage loss in OA.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10142591PMC
http://dx.doi.org/10.3390/ijms24087532DOI Listing

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