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Establishment of an Ex Vivo Inflammatory Osteoarthritis Model With Human Osteochondral Explants

Kaihu Li, Penghui Zhang, Yong Zhu, Mauro Alini, Sibylle Grad, Zhen Li

2021Frontiers in Bioengineering and Biotechnology15 citationsDOIOpen Access PDF

Abstract

Osteoarthritis (OA) is the most common degenerative joint disease without clear pathophysiological mechanism and effective drugs for treatment. Although various animal models exist, the translation of the outcome into clinics remains difficult due to species differences. In this study, an ex vivo inflammatory OA model was induced using different concentrations of interleukin one beta (IL-1 β ) and tumor necrosis factor α (TNF-α) on explants from the human femoral head. In the inflammatory OA groups, the gene expression levels of cartilage catabolism (matrix metalloproteinase 1 (MMP1), matrix metalloproteinase 3 (MMP3)), and inflammation (interleukin 6 (IL-6), interleukin 8 (IL-8)) markers were significantly upregulated, while the anabolic genes (collagen 2 (COL2), aggrecan (ACAN), and proteoglycan 4 (PRG4)) were downregulated compared to the control group. The release of cytokines (IL-6, IL-8) and nitric oxide (NO) in the conditioned medium was also upregulated in inflammatory OA groups. The Safranin O/Fast Green staining showed loss of proteoglycan in the superficial zone cartilage after cytokine treatment. The results indicated that an ex vivo inflammation and degeneration model was successfully established using osteochondral explants from the human femoral head. This model can be used to elucidate the in-depth mechanism of inflammatory OA and to screen new drugs for OA treatment.

Topics & Concepts

AggrecanEx vivoMMP3InflammationCartilageInterleukinOsteoarthritisMedicineMatrix metalloproteinaseProteoglycanImmunologyDownregulation and upregulationTumor necrosis factor alphaIn vivoCytokinePathologyChemistryInternal medicineBiologyGene expressionAnatomyBiochemistryArticular cartilageAlternative medicineBiotechnologyGeneOsteoarthritis Treatment and MechanismsInflammatory mediators and NSAID effectsProtease and Inhibitor Mechanisms
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