连续施加循环机械载荷对关节软骨外植体纤维连接蛋白代谢的影响。

J Steinmeyer, B Ackermann
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引用次数: 18

摘要

关节软骨主要作为一种承重材料,能够调节其自身的代谢活动,以响应所施加的机械刺激。纤维连接蛋白在软骨细胞外基质的组织和功能中起着关键作用。本研究的目的是系统地研究负载强度、频率和持续时间对成熟牛关节软骨外植体合成、含量和释放纤维连接蛋白和蛋白质的影响。增加负载强度和负载时间,抑制纤维连接蛋白和蛋白质的合成和含量;纤维连接蛋白的合成比整体蛋白质的合成受到更特异性的影响,这表明纤维连接蛋白比其他蛋白质的合成对压力的反应更灵敏。即使外植体受到更大的压缩,降低加载频率也不能调节给定循环胁迫对纤维连接蛋白和蛋白质合成和含量的抑制作用。与未加载对照相比,内源性纤维连接蛋白的释放显著减少,与加载方案无关。该研究表明,负载的大小和持续时间影响纤维连接蛋白和蛋白质合成的抑制程度,而负载的外植体具有提高但有限的结合纤维连接蛋白的能力。与其他研究相比,我们目前的研究结果表明,施加的负荷功能对软骨细胞的代谢有深远的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The effect of continuously applied cyclic mechanical loading on the fibronectin metabolism of articular cartilage explants.

Articular cartilage serves primarily as a load-bearing material able to regulate its own metabolic activity in response to the mechanical stimuli applied. Fibronectin plays a critical role in the organization and function of the cartilage extracellular matrix. The purpose of this study was to investigate systematically the effect of load magnitude, frequency and duration of loading on the synthesis, content and release of fibronectin and proteins by mature bovine articular cartilage explants using a novel mechanical loading system. Increasing the load magnitude, as well as the duration of loading, inhibited the synthesis and content of fibronectin and proteins; the fibronectin synthesis was more specifically affected than the overall protein synthesis indicating that fibronectin is more responsive to pressure than synthesis of other proteins. Reducing the load frequency did not modulate the inhibitory effect of a given cyclic stress on synthesis and content of fibronectin and proteins even though explants were more compressed. The release of endogenous fibronectin was significantly reduced independent of the applied loading protocols when compared with unloaded controls. This study demonstrates that the magnitude and the duration of loading influences the degree of inhibition of fibronectin and protein synthesis, while loaded explants possess an elevated but limited capacity to bind fibronectin. Compared with other studies, our present results show that the applied load function in particular has a profound effect on the metabolism of chondrocytes.

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