Piergiovanni Monica, Galli Valeria, Holzner Gregor, Stavrakis Stavros, DeMello Andrew, Dubini Gabriele
Laboratory of Biological Structure Mechanics (LaBS), Department of Chemistry, Materials and Chemical Engineering "Giulio Natta", Politecnico di Milano, piazza Leonardo da Vinci, 32 - 20133 Milan, Italy.
Lab Chip. 2020 Jul 14;20(14):2539-2548. doi: 10.1039/d0lc00166j.
The mechanical properties of cells are of enormous interest in a diverse range of physio and pathological situations of clinical relevance. Unsurprisingly, a variety of microfluidic platforms have been developed in recent years to study the deformability of cells, most commonly employing pure shear or extensional flows, with and without direct contact of the cells with channel walls. Herein, we investigate the effects of shear and extensional flow components on fluid-induced cell deformation by means of three microchannel geometries. In the case of hyperbolic microchannels, cell deformation takes place in a flow with constant extensional rate, under non-zero shear conditions. A sudden expansion at the microchannel terminus allows one to evaluate shape recovery subsequent to deformation. Comparison with other microchannel shapes, that induce either pure shear (straight channel) or pure extensional (cross channel) flows, reveals different deformation modes. Such an analysis is used to confirm the softening and stiffening effects of common treatments, such as cytochalasin D and formalin on cell deformability. In addition to an experimental analysis of leukaemia cell deformability, computational fluid dynamic simulations are used to deconvolve the role of the aforementioned flow components in the cell deformation dynamics. In general terms, the current study can be used as a guide for extracting deformation/recovery dynamics of leukaemia cell lines when exposed to various fluid dynamic conditions.
细胞的力学特性在一系列具有临床相关性的生理和病理状况中备受关注。不出所料,近年来已开发出多种微流控平台来研究细胞的可变形性,最常见的是采用纯剪切或拉伸流,细胞与通道壁有无直接接触。在此,我们借助三种微通道几何形状研究剪切和拉伸流分量对流体诱导细胞变形的影响。在双曲线形微通道的情况下,细胞变形发生在具有恒定拉伸速率的流中,处于非零剪切条件下。微通道末端的突然扩张使得能够评估变形后的形状恢复情况。与其他诱导纯剪切(直通道)或纯拉伸(十字通道)流的微通道形状进行比较,揭示了不同的变形模式。这种分析用于确认常见处理(如细胞松弛素D和福尔马林)对细胞可变形性的软化和硬化作用。除了对白血病细胞可变形性进行实验分析外,还使用计算流体动力学模拟来剖析上述流分量在细胞变形动力学中的作用。总体而言,当前研究可作为在白血病细胞系暴露于各种流体动力学条件时提取其变形/恢复动力学的指南。