Differential Effects of Hypoxia versus Hyperoxia or Physoxia on Phenotype and Energy Metabolism in Human Chondrocytes from Osteoarthritic Compared to Macroscopically Normal Cartilage

Author:

Jain Lekha1,Bolam Scott M.23,Monk A. Paul4,Munro Jacob T.2,Chen Even1,Tamatea Jade5,Dalbeth Nicola3,Poulsen Raewyn C.1ORCID

Affiliation:

1. Department of Pharmacology and Clinical Pharmacology, University of Auckland, Auckland 1023, New Zealand

2. Department of Surgery, University of Auckland, Auckland 1023, New Zealand

3. Department of Medicine, University of Auckland, Auckland 1023, New Zealand

4. Auckland Bioengineering Institute, University of Auckland, Auckland 1010, New Zealand

5. Te Kupenga Hauora Māori, University of Auckland, Auckland 1010, New Zealand

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.

Funder

Health Research Council of New Zealand

Publisher

MDPI AG

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis

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