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软骨细胞聚集蛋白聚糖和II型胶原蛋白基因表达的下调与静态压缩强度和持续时间的增加相关。

Down-regulation of chondrocyte aggrecan and type-II collagen gene expression correlates with increases in static compression magnitude and duration.

作者信息

Ragan P M, Badger A M, Cook M, Chin V I, Gowen M, Grodzinsky A J, Lark M W

机构信息

Department of Electrical Engineering and Computer Science, Center for Biomedical Engineering, Massachusetts Institute of Technology, Cambridge 02139, USA.

出版信息

J Orthop Res. 1999 Nov;17(6):836-42. doi: 10.1002/jor.1100170608.

Abstract

The goal of this study was to examine the simultaneous effects of mechanical compression of chondrocytes on mRNA expression and macromolecular synthesis of aggrecan and type-II collagen. Bovine cartilage explants were exposed to different magnitudes and durations of applied mechanical compression, and levels of aggrecan and type-IIa collagen mRNA normalized to glyceraldehyde-3-phosphate dehydrogenase were measured and quantified by Northern blot analysis. Synthesis of aggrecan and type-II collagen protein was measured by radiolabel incorporation of [35S]sulfate and [3H]proline into macromolecules. The results showed a dose-dependent decrease in mRNA levels for aggrecan and type-II collagen, with increasing compression relative to physiological cut thickness applied for 24 hours. Radiolabel incorporation into glycosaminoglycans and collagen also decreased with increasing compression in a dose-related manner similar to the changes seen in mRNA expression. The modulation of aggrecan and type-II collagen mRNA and protein synthesis were dependent on the duration of the compression. Aggrecan and type-II collagen mRNA expression increased during the initial 0.5 hours of static compression; however, 4-24 hours after compression was applied total mRNA levels had significantly decreased. The synthesis of aggrecan and collagen protein decreased more rapidly than did mRNA levels after the application of a step compression. Together, these results suggest that mechanical compression rapidly alters chondrocyte aggrecan and type-II collagen gene expression on application of load. However, our results indicate that the observed decreases in biosynthesis may not be related solely to changes in mRNA expression. The mechanisms by which mechanical forces affect different segments of the biosynthetic pathways remain to be determined.

摘要

本研究的目的是检测机械压缩软骨细胞对聚集蛋白聚糖和Ⅱ型胶原蛋白的mRNA表达及大分子合成的同时影响。将牛软骨外植体暴露于不同强度和持续时间的机械压缩下,通过Northern印迹分析测量并定量以甘油醛-3-磷酸脱氢酶标准化的聚集蛋白聚糖和Ⅱ型胶原蛋白mRNA水平。通过将[35S]硫酸盐和[3H]脯氨酸放射性标记掺入大分子中来测量聚集蛋白聚糖和Ⅱ型胶原蛋白的合成。结果显示,与施加24小时的生理切割厚度相比,随着压缩增加,聚集蛋白聚糖和Ⅱ型胶原蛋白的mRNA水平呈剂量依赖性降低。放射性标记掺入糖胺聚糖和胶原蛋白的量也随着压缩增加而以与mRNA表达变化相似的剂量相关方式降低。聚集蛋白聚糖和Ⅱ型胶原蛋白mRNA及蛋白质合成的调节取决于压缩的持续时间。在静态压缩的最初0.5小时内,聚集蛋白聚糖和Ⅱ型胶原蛋白mRNA表达增加;然而,施加压缩4 - 24小时后,总mRNA水平显著降低。施加阶跃压缩后,聚集蛋白聚糖和胶原蛋白的合成比mRNA水平下降得更快。总之,这些结果表明,施加负荷时机械压缩会迅速改变软骨细胞聚集蛋白聚糖和Ⅱ型胶原蛋白的基因表达。然而,我们的结果表明,观察到的生物合成减少可能不仅仅与mRNA表达的变化有关。机械力影响生物合成途径不同环节的机制仍有待确定。

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