Maul Timothy M, Hamilton Douglas W, Nieponice Alejandro, Soletti Lorenzo, Vorp David A
Department of Surgery, and the McGowan Institute for Regenerative Medicine, University of Pittsburgh, 100 Technology Drive, Suite 200, Pittsburgh, PA 15219, USA.
J Biomech Eng. 2007 Feb;129(1):110-6. doi: 10.1115/1.2401190.
Mechanical forces have been shown to be important stimuli for the determination and maintenance of cellular phenotype and function. Many cells are constantly exposed in vivo to cyclic pressure, shear stress, and/or strain. Therefore, the ability to study the effects of these stimuli in vitro is important for understanding how they contribute to both normal and pathologic states. While there exist commercial as well as custom-built devices for the extended application of cyclic strain and shear stress, very few cyclic pressure systems have been reported to apply stimulation longer than 48 h. However, pertinent responses of cells to mechanical stimulation may occur later than this. To address this limitation, we have designed a new cyclic hydrostatic pressure system based upon the following design variables: minimal size, stability of pressure and humidity, maximal accessibility, and versatility. Computational fluid dynamics (CFD) was utilized to predict the pressure and potential shear stress within the chamber during the first half of a 1.0 Hz duty cycle. To biologically validate our system, we tested the response of bone marrow progenitor cells (BMPCs) from Sprague Dawley rats to a cyclic pressure stimulation of 120/80 mm Hg, 1.0 Hz for 7 days. Cellular morphology was measured using Scion Image, and cellular proliferation was measured by counting nuclei in ten fields of view. CFD results showed a constant pressure across the length of the chamber and no shear stress developed at the base of the chamber where the cells are cultured. BMPCs from Sprague Dawley rats demonstrated a significant change in morphology versus controls by reducing their size and adopting a more rounded morphology. Furthermore, these cells increased their proliferation under cyclic hydrostatic pressure. We have demonstrated that our system imparts a single mechanical stimulus of cyclic hydrostatic pressure and is capable of at least 7 days of continuous operation without affecting cellular viability. Furthermore, we have shown for the first time that BMPCs respond to cyclic hydrostatic pressure by alterations in morphology and increased proliferation.
机械力已被证明是决定和维持细胞表型及功能的重要刺激因素。许多细胞在体内持续受到循环压力、剪切应力和/或应变的作用。因此,在体外研究这些刺激因素的作用对于理解它们如何导致正常和病理状态都很重要。虽然存在用于长时间施加循环应变和剪切应力的商业及定制设备,但据报道,很少有循环压力系统能施加超过48小时的刺激。然而,细胞对机械刺激的相关反应可能在此之后才会出现。为解决这一限制,我们基于以下设计变量设计了一种新型循环静水压力系统:最小尺寸、压力和湿度稳定性、最大可达性以及多功能性。利用计算流体动力学(CFD)预测在1.0赫兹占空比的前半周期内腔室内的压力和潜在剪切应力。为从生物学角度验证我们的系统,我们测试了来自Sprague Dawley大鼠的骨髓祖细胞(BMPC)对120/80毫米汞柱、1.0赫兹的循环压力刺激7天的反应。使用Scion Image测量细胞形态,通过在十个视野中计数细胞核来测量细胞增殖。CFD结果显示腔室全长压力恒定,在培养细胞的腔室底部未产生剪切应力。来自Sprague Dawley大鼠的BMPC与对照组相比,形态发生了显著变化,细胞尺寸减小并呈现出更圆润的形态。此外,这些细胞在循环静水压力下增殖增加。我们已经证明,我们的系统能够施加单一的循环静水压力机械刺激,并且能够连续运行至少7天而不影响细胞活力。此外,我们首次表明BMPC通过形态改变和增殖增加对循环静水压力作出反应。