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单轴细胞拉伸仪的设计与构建。

Design and construction of a uniaxial cell stretcher.

作者信息

Yost M J, Simpson D, Wrona K, Ridley S, Ploehn H J, Borg T K, Terracio L

机构信息

Department of Developmental Biology and Anatomy, University of South Carolina School of Medicine, Columbia, South Carolina 29208, USA.

出版信息

Am J Physiol Heart Circ Physiol. 2000 Dec;279(6):H3124-30. doi: 10.1152/ajpheart.2000.279.6.H3124.

DOI:10.1152/ajpheart.2000.279.6.H3124
PMID:11087271
Abstract

In vitro mechanical cell stimulators are used for the study of the effect of mechanical stimulation on anchorage-dependent cells. We developed a new mechanical cell stimulator, which uses stepper motor technology and computer control to achieve a high degree of accuracy and repeatability. This device also uses high-performance plastic components that have been shown to be noncytotoxic, dimensionally stable, and resistant to chemical degradation from common culture laboratory chemicals. We show that treatment with glow discharge for 25 s at 20 mA is sufficient to modify the surface of the rubber to allow proper adhesion for polymerization of aligned collagen. We show through finite element analysis that the middle area of the membrane, away from the clamped ends, is predictable, homogeneous, and has negligible shear strain. To test the efficacy of the mechanical stretch, we examined the effect of mechanical stimulation on the production of beta(1)-integrin by neonatal rat cardiac fibroblasts. Mechanical stimulation was tested in the range of 0-12% stretch and 0-10-cycles/min stretch frequency. The fibroblasts respond with an increase in beta(1)-integrin at 3% stretch and a decrease at 6 and 12% stretch. Stretch frequency was found to not significantly effect the concentration of beta(1)-integrin. These studies yield a new and improved mechanical cell stimulator and demonstrate that mechanical stimulation has an effect on the expression of beta(1)-integrin.

摘要

体外机械细胞刺激器用于研究机械刺激对贴壁依赖性细胞的影响。我们开发了一种新型机械细胞刺激器,它采用步进电机技术和计算机控制,以实现高度的准确性和可重复性。该装置还使用了高性能塑料部件,这些部件已被证明无细胞毒性、尺寸稳定,并且能抵抗常见培养实验室化学物质的化学降解。我们表明,在20 mA下进行25 s的辉光放电处理足以改变橡胶表面,以便使对齐的胶原蛋白聚合能够正常粘附。我们通过有限元分析表明,膜的中间区域远离夹紧端,是可预测的、均匀的,并且剪切应变可忽略不计。为了测试机械拉伸的效果,我们研究了机械刺激对新生大鼠心脏成纤维细胞β(1)整合素产生的影响。在0 - 12%拉伸范围和0 - 10次/分钟拉伸频率下测试了机械刺激。成纤维细胞在3%拉伸时β(1)整合素增加,在6%和12%拉伸时减少。发现拉伸频率对β(1)整合素的浓度没有显著影响。这些研究产生了一种新的、改进的机械细胞刺激器,并证明机械刺激对β(1)整合素的表达有影响。

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