一种新型装置拉伸多种组织样品与可变模式:mRNA调控在组织工程构建中的应用。

Biomatter Pub Date : 2013-07-01 Epub Date: 2013-04-01 DOI:10.4161/biom.24650
Jasmin Imsirovic, Kelsey Derricks, Jo Ann Buczek-Thomas, Celeste B Rich, Matthew A Nugent, Béla Suki
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引用次数: 20

摘要

在体内,特别是在呼吸和循环系统中,许多细胞受到不规则的时变机械刺激。机械拉伸是决定细胞功能的重要因素;然而,可变拉伸的影响仍未被探索。为了研究可变拉伸的影响,我们设计、制造并测试了一种单轴拉伸装置,该装置可以在不同周期改变应变幅值的情况下拉伸三维组织结构。该设备是第一个将可变拉伸信号应用于组织细胞或三维组织结构的设备。在设备验证后,我们将20%单轴应变应用于含有不同变异性水平(0%,25%,50%和75%)的新生大鼠肺成纤维细胞的明胶泡沫样品。然后采用RT-PCR测量可变拉伸对参与细胞-基质相互作用的关键分子的影响,包括:胶原1α、赖氨酸氧化酶、α-肌动蛋白、β1整合素、β3整合素、syndecan-4和血管内皮生长因子-a。根据分子和变异性的大小,增加拉伸信号的变异性对mRNA的产生有上调、下调或无影响。特别是syndecan-4,其变异率达到了25%,这表明菌株的最佳变异可能存在于该分子的生产中。我们得出结论,菌株的周期变异性影响与细胞-基质相互作用相关的分子的表达,因此可以用来选择性地调整组织结构的组成。
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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A novel device to stretch multiple tissue samples with variable patterns: application for mRNA regulation in tissue-engineered constructs.

A broad range of cells are subjected to irregular time varying mechanical stimuli within the body, particularly in the respiratory and circulatory systems. Mechanical stretch is an important factor in determining cell function; however, the effects of variable stretch remain unexplored. In order to investigate the effects of variable stretch, we designed, built and tested a uniaxial stretching device that can stretch three-dimensional tissue constructs while varying the strain amplitude from cycle to cycle. The device is the first to apply variable stretching signals to cells in tissues or three dimensional tissue constructs. Following device validation, we applied 20% uniaxial strain to Gelfoam samples seeded with neonatal rat lung fibroblasts with different levels of variability (0%, 25%, 50% and 75%). RT-PCR was then performed to measure the effects of variable stretch on key molecules involved in cell-matrix interactions including: collagen 1α, lysyl oxidase, α-actin, β1 integrin, β3 integrin, syndecan-4, and vascular endothelial growth factor-A. Adding variability to the stretching signal upregulated, downregulated or had no effect on mRNA production depending on the molecule and the amount of variability. In particular, syndecan-4 showed a statistically significant peak at 25% variability, suggesting that an optimal variability of strain may exist for production of this molecule. We conclude that cycle-by-cycle variability in strain influences the expression of molecules related to cell-matrix interactions and hence may be used to selectively tune the composition of tissue constructs.

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