Effects of Low Oxygen Tension during Expansion on Chondrogenic Potential of Osteoarthritic Chondrocytes

Jing Wang, K. A. Davis, J. H. Henderson
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Abstract

Primary human chondrocytes, although a promising cell source for cartilage tissue engineering, tend to dedifferentiate and lose their characteristic gene expression and protein production during monolayer expansion. Low O2 tension in vitro culture has been studied to examine its effect on preventing dedifferentiation, and results have been conflicting. In particular, low O2 expansion effects on human osteoarthritis (OA) chondrocytes are poorly understood. In this study, we expanded chondrocytes collected from patients with osteoarthritis (OA) under normal (21%) and low (5%) O2 tension then continued with micromass culture under 21% O2 for 3 weeks. Our results suggest that low O2 condition may promote chondrogenic characteristic gene expression in monolayer cells. But improved ECM production, which was seen earlier in animal models, may not be relevant to human OA chondrocytes. Further examination of the mechanical properties of the engineered pellets is needed to confirm the effects of low O2 expansion on human OA chondrocytes and their use in cartilage tissue engineering.
扩张时低氧张力对骨关节炎软骨细胞成软骨潜能的影响
原代人软骨细胞虽然是软骨组织工程中很有前途的细胞来源,但在单层扩增过程中容易去分化并失去其特有的基因表达和蛋白质产生。低氧张力的体外培养研究了其对阻止去分化的作用,结果相互矛盾。特别是,低氧扩张对人类骨关节炎(OA)软骨细胞的影响尚不清楚。在这项研究中,我们在正常(21%)和低(5%)氧张力下对骨关节炎(OA)患者的软骨细胞进行扩增,然后在21%的氧张力下继续进行微质量培养3周。我们的研究结果表明,低氧条件可能促进单层细胞软骨形成特征基因的表达。但是早期在动物模型中观察到的ECM生成的改善可能与人类OA软骨细胞无关。需要进一步研究工程微球的力学性能,以确认低氧膨胀对人OA软骨细胞的影响及其在软骨组织工程中的应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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