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一种用于以可变模式拉伸多个组织样本的新型装置:在组织工程构建物中对mRNA调控的应用。

A novel device to stretch multiple tissue samples with variable patterns: application for mRNA regulation in tissue-engineered constructs.

作者信息

Imsirovic Jasmin, Derricks Kelsey, Buczek-Thomas Jo Ann, Rich Celeste B, Nugent Matthew A, Suki Béla

机构信息

Department of Biomedical Engineering; Boston University; Boston, MA USA.

Department of Biochemistry; Boston University School of Medicine; Boston, MA USA.

出版信息

Biomatter. 2013 Jul-Sep;3(3). doi: 10.4161/biom.24650. Epub 2013 Apr 1.

Abstract

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.

摘要

体内多种细胞会受到不规则的随时间变化的机械刺激,尤其是在呼吸系统和循环系统中。机械拉伸是决定细胞功能的一个重要因素;然而,可变拉伸的影响仍未得到探索。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,该装置可以在逐周期改变应变幅度的同时对三维组织构建体进行拉伸。该装置是首个将可变拉伸信号施加于组织或三维组织构建体中的细胞的装置。在装置验证之后,我们对接种了新生大鼠肺成纤维细胞且具有不同可变水平(0%、25%、50%和75%)的明胶海绵样本施加20%的单轴应变。然后进行逆转录聚合酶链反应(RT-PCR)以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,这些分子包括:胶原蛋白1α、赖氨酰氧化酶、α-肌动蛋白、β1整合素、β3整合素、多功能蛋白聚糖-4和血管内皮生长因子-A。根据分子和可变程度,向拉伸信号中添加可变因素会上调、下调或对信使核糖核酸(mRNA)产生没有影响。特别是,多功能蛋白聚糖-4在25%的可变程度时显示出具有统计学意义的峰值,这表明该分子的产生可能存在一个最佳的应变可变程度。我们得出结论,应变的逐周期变化会影响与细胞-基质相互作用相关分子的表达,因此可用于选择性地调节组织构建体的组成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c5d/3749279/ab8e093aafc4/biom-3-e24650-g1.jpg

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