LAAS-CNRS , Université de Toulouse, CNRS, INSA , Toulouse 31031 , France.
Institut de Pharmacologie et de Biologie Structurale, Université de Toulouse, CNRS, UPS , Toulouse 31077 , France.
Nano Lett. 2018 Oct 10;18(10):6326-6333. doi: 10.1021/acs.nanolett.8b02611. Epub 2018 Sep 27.
In vivo, immune cells migrate through a wide variety of tissues, including confined and constricting environments. Deciphering how cells apply forces when infiltrating narrow areas is a critical issue that requires innovative experimental procedures. To reveal the distribution and dynamics of the forces of cells migrating in confined environments, we designed a device combining microchannels of controlled dimensions with integrated deformable micropillars serving as sensors of nanoscale subcellular forces. First, a specific process composed of two steps of photolithography and dry etching was tuned to obtain micrometric pillars of controlled stiffness and dimensions inside microchannels. Second, an image-analysis workflow was developed to automatically evaluate the amplitude and direction of the forces applied on the micropillars by migrating cells. Using this workflow, we show that this microdevice is a sensor of forces with a limit of detection down to 64 pN. Third, by recording pillar movements during the migration of macrophages inside the confining microchannels, we reveal that macrophages bent the pillars with typical forces of 0.3 nN and applied higher forces at the cell edges than around their nuclei. When the degree of confinement was increased, we found that forces were redirected from inward to outward. By providing a microdevice that allows the analysis of force direction and force magnitude developed by confined cells, our work paves the way for investigating the mechanical behavior of cells migrating though 3D constricted environments.
在体内,免疫细胞通过各种组织迁移,包括受限和狭窄的环境。破译细胞在渗透狭窄区域时如何施加力是一个关键问题,需要创新的实验程序。为了揭示在受限环境中迁移的细胞的力的分布和动态,我们设计了一种将具有受控尺寸的微通道与作为纳米级亚细胞力传感器的集成可变形微柱结合在一起的设备。首先,我们调整了由两步光刻和干法刻蚀组成的特定工艺,以在微通道内获得具有受控刚度和尺寸的微柱。其次,开发了一种图像分析工作流程,以自动评估迁移细胞施加在微柱上的力的幅度和方向。使用此工作流程,我们表明该微设备是一种力传感器,其检测限低至 64 pN。第三,通过记录巨噬细胞在限制微通道内迁移过程中支柱的运动,我们发现巨噬细胞弯曲支柱,典型力为 0.3 nN,并且在细胞边缘施加的力大于其核周围的力。当限制程度增加时,我们发现力从内向外地重新定向。通过提供一种允许分析受限细胞产生的力方向和力大小的微设备,我们的工作为研究通过 3D 狭窄环境迁移的细胞的机械行为铺平了道路。