Key result
Cultivation of human articular chondrocytes under hypoxia (5% O2) increased expression of hypoxia-inducible factors and extracellular matrix accumulation compared with normoxia.
Why the study?
Does cultivation under hypoxic conditions improve zonal marker expression in human articular chondrocytes compared to normoxic conditions?
Does cultivation under hypoxic conditions improve zonal marker expression in human articular chondrocytes compared to normoxic conditions?
Cultivating human articular chondrocytes under hypoxic conditions helps retain important zonal phenotypic differences, which is critical for engineering cartilage tissue.
May support hypoxic culture for cartilage engineering; hypothesis-generating for zonal phenotype retention in vivo.
Articular cartilage is organized in depth zones with phenotypically distinct subpopulations of chondrocytes that are exposed to different oxygen tensions. Despite growing evidence of the critical role for oxygen in chondrogenesis, little is known about its effect on chondrocytes from different zones. This study evaluates zonal marker expression of human articular chondrocytes from different zones under various oxygen tensions. Chondrocytes isolated from full-thickness, superficial, and middle/deep cartilage from knee replacement surgeries were expanded and redifferentiated under hypoxic (5% O(2)) or normoxic (20% O(2)) conditions. Differentiation under hypoxia increased expression of hypoxia-inducible factors 1alpha and 2alpha and accumulation of extracellular matrix, particularly in middle/deep chondrocytes, and favored re-expression of proteoglycan 4 by superficial chondrocytes compared with middle/deep cells. Zone-dependent expression of clusterin varied with culture duration. These results demonstrate that zonal chondrocytes retain important phenotypic differences during in vitro cultivation, and that these characteristics can be improved by altering the oxygen environment. However, transcript levels for pleiotrophin, cartilage intermediate layer protein, and collagen type X were similar between zones, challenging their reliability as zonal markers for tissue-engineered cartilage from osteoarthritis patients. Key factors including oxygen tension and cell source should be considered to prescribe zone-specific properties to tissue-engineered cartilage.
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Schrobback et al. (2011) studied Osteoarthritis. Hypoxia (5% O2) vs. Normoxia (20% O2) was evaluated on Zonal marker expression and extracellular matrix accumulation. Cultivation of human articular chondrocytes under hypoxia (5% O2) increased expression of hypoxia-inducible factors and extracellular matrix accumulation compared with normoxia.
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