Department of Biomedical Engineering, Case Western Reserve University, Cleveland, Ohio, USA.
PLoS One. 2010 Sep 17;5(9):e12796. doi: 10.1371/journal.pone.0012796.
A major hurdle to understanding and exploiting interactions between the stem cell and its environment is the lack of a tool for precise delivery of mechanical cues concomitant to observing sub-cellular adaptation of structure. These studies demonstrate the use of microscale particle image velocimetry (μ-PIV) for in situ spatiotemporal mapping of flow fields around mesenchymal stem cells, i.e. murine embryonic multipotent cell line C3H10T1/2, at the subcellular length scale, providing a tool for real time observation and analysis of stem cell adaptation to the prevailing mechanical milieu. In the absence of cells, computational fluid dynamics (CFD) predicts flow regimes within 12% of μ-PIV measures, achieving the technical specifications of the chamber and the flow rates necessary to deliver target shear stresses at a particular height from the base of the flow chamber. However, our μ-PIV studies show that the presence of cells per se as well as the density at which cells are seeded significantly influences local flow fields. Furthermore, for any given cell or cell seeding density, flow regimes vary significantly along the vertical profile of the cell. Hence, the mechanical milieu of the stem cell exposed to shape changing shear stresses, induced by fluid drag, varies with respect to proximity of surrounding cells as well as with respect to apical height. The current study addresses a previously unmet need to predict and observe both flow regimes as well as mechanoadaptation of cells in flow chambers designed to deliver precisely controlled mechanical signals to live cells. An understanding of interactions and adaptation in response to forces at the interface between the surface of the cell and its immediate local environment may be key for de novo engineering of functional tissues from stem cell templates as well as for unraveling the mechanisms underlying multiscale development, growth and adaptation of organisms.
理解和利用干细胞与其环境之间的相互作用的一个主要障碍是缺乏一种工具,无法在观察亚细胞结构适应的同时精确传递机械线索。这些研究表明,微尺度粒子图像测速(μ-PIV)可用于原位时空映射间充质干细胞周围的流场,即鼠胚胎多能细胞系 C3H10T1/2,在亚细胞长度尺度上,为实时观察和分析干细胞对流行的机械环境的适应提供了一种工具。在没有细胞的情况下,计算流体动力学(CFD)预测的流型与 μ-PIV 测量值相差 12%以内,达到了腔室的技术规格和所需的流速,可在流动腔室底部特定高度处输送目标剪切应力。然而,我们的 μ-PIV 研究表明,细胞的存在本身以及细胞接种的密度都会显著影响局部流场。此外,对于任何给定的细胞或细胞接种密度,流型沿细胞的垂直剖面变化很大。因此,暴露于由流体阻力引起的形状变化剪切应力下的干细胞的机械环境会根据周围细胞的接近程度以及顶端高度而变化。本研究满足了以前未满足的需求,即预测和观察流动腔室内的流型以及细胞的机械适应,这些腔室旨在向活细胞精确传递机械信号。了解细胞表面与其直接局部环境之间界面处的相互作用和适应对于从头设计功能组织的干细胞以及揭示多尺度发育、生长和适应的机制可能是关键。