Dynamic Hydrostatic Pressurization Increases Matrix Gene Expression by Chondrocytes in 3D Culture

R. Mauck, M. Soltz, G. Ateshian, C. Hung
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引用次数: 1

Abstract

Articular cartilage is the load-bearing substance that covers the bony surfaces of articulating bones. With its high water content and small pore size, deformation of cartilage induces a very high hydrostatic pressure within the cartilage. This hydrostatic pressure has been shown both theoretically and experimentally to support upwards of 90% of the applied load (1), and can be on the order of 6–12 MPa. Chondrocytes, the cells within cartilage respond to this pressure by altering their rates of biosynthesis. Studies utilizing radionucleotide incorporation in both explant and monolayer cultures (2–4) have shown that in general dynamic pressurization increases synthesis, while static pressurization decreases synthesis. More recently, Smith et al have shown that dynamic pressurization (10MPa, 1 Hz) of cells in monolayer culture can upregulate matrix gene expression (5,6). Further, a study in PGA constructs has shown that long term application of dynamic pressure can increase matrix deposition (7). In this study, we seek to expand on these findings by examining the response in gene expression of articular chondrocytes encapsulated in alginate, a charged, 3D hydrogel.
动态静水加压增加三维培养软骨细胞基质基因表达
关节软骨是覆盖在关节骨表面的承重物质。软骨的高含水量和小孔径,使其变形在软骨内部产生非常高的静水压力。这个静水压力在理论和实验上都被证明可以支撑90%以上的载荷(1),并且可以在6-12兆帕的量级上。软骨细胞,软骨内的细胞通过改变它们的生物合成速率来应对这种压力。在外植体和单层培养中利用放射性核苷酸掺入的研究(2-4)表明,通常动态加压会增加合成,而静态加压会减少合成。最近,Smith等人发现单层培养细胞的动态加压(10MPa, 1hz)可以上调基质基因表达(5,6)。此外,一项关于PGA结构的研究表明,长期应用动压可以增加基质沉积(7)。在本研究中,我们试图通过检测海藻酸盐(一种带电的3D水凝胶)包裹的关节软骨细胞对基因表达的反应来扩展这些发现。
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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