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骨形态发生蛋白-2对长期培养的关节软骨细胞细胞外基质、材料特性及基因表达的影响:软骨细胞稳定性丧失

Influence of bone morphogenetic protein-2 on the extracellular matrix, material properties, and gene expression of long-term articular chondrocyte cultures: loss of chondrocyte stability.

作者信息

Krawczak David A, Westendorf Jennifer J, Carlson Cathy S, Lewis Jack L

机构信息

Department of Orthopaedic Surgery, University of Minnesota, Minneapolis, Minnesota 55455, USA.

出版信息

Tissue Eng Part A. 2009 Jun;15(6):1247-55. doi: 10.1089/ten.tea.2008.0249.

Abstract

The aim of this study was to determine the effects of bone morphogenetic protein-2 (BMP-2) on articular chondrocyte tissues grown as monolayers in vitro for up to 8 weeks. Articular chondrocytes were isolated from New Zealand White rabbits and plated in monolayer cultures. The cultures were supplemented with 100 ng/mL of BMP-2 for up to 8 weeks and the extracellular matrix (ECM) composition, material properties, and messenger RNA (mRNA) expression were analyzed. mRNA expression of cartilage-specific genes, type II collagen, and aggrecan showed that BMP-2 enhanced chondrocyte stability for up to 3 weeks. After 3 weeks in culture, there was substantially more type I collagen expression and more osteopontin and runt-related transcription factor 2 expression in 5- and 8-week cultures treated with BMP-2 than in controls. Additionally, matrix metalloproteinase-13 and ADAMTS-5 (A disintegrin-like and metalloproteinase with thrombospondin 5) were upregulated in 5- and 8-week cultures treated with BMP-2, coinciding with a loss of ECM density, collagen, and proteoglycan. Eight-week tissue stimulated with BMP-2 was more fragile and tore more easily when removed from the culture dish as compared to controls, suggesting temporal limitations to the effectiveness of BMP-2 in monolayer systems and perhaps other models to enhance the generation of a cartilage-like tissue for tissue engineering purposes.

摘要

本研究的目的是确定骨形态发生蛋白-2(BMP-2)对体外单层培养长达8周的关节软骨细胞组织的影响。从新西兰白兔中分离出关节软骨细胞,并接种于单层培养物中。向培养物中添加100 ng/mL的BMP-2,持续8周,并分析细胞外基质(ECM)组成、材料特性和信使核糖核酸(mRNA)表达。软骨特异性基因、II型胶原蛋白和聚集蛋白聚糖的mRNA表达表明,BMP-2可增强软骨细胞稳定性长达3周。培养3周后,与对照组相比,用BMP-2处理的5周和8周培养物中I型胶原蛋白表达显著增加,骨桥蛋白和 runt相关转录因子2表达更多。此外,在5周和8周用BMP-2处理的培养物中,基质金属蛋白酶-13和含血小板反应蛋白基序的解聚素样金属蛋白酶5(ADAMTS-5)上调,这与ECM密度、胶原蛋白和蛋白聚糖的减少相一致。与对照组相比,用BMP-2刺激8周的组织更脆弱,从培养皿中取出时更容易撕裂,这表明BMP-2在单层系统以及可能在其他模型中,对于增强用于组织工程目的的类软骨组织生成的有效性存在时间限制。

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