Tibbitt Mark W, Kloxin April M, Dyamenahalli Kiran U, Anseth Kristi S
Department of Chemical and Biological Engineering, University of Colorado, Boulder, CO.
Soft Matter. 2010;6(20):5100-5108. doi: 10.1039/C0SM00174K.
Cell adhesion and detachment to and from the extracellular matrix (ECM) are critical regulators of cell function and fate due to the exchange of mechanical signals between the cell and its microenvironment. To study this cell mechanobiology, researchers have developed several innovative methods to investigate cell adhesion in vitro; however, most of these culture platforms are unnaturally stiff or static. To better capture the soft, dynamic nature of the ECM, we present a PEG-based hydrogel in which the context and geometry of the extracellular space can be precisely controlled in situ via two-photon induced erosion. Here, we characterize the two-photon erosion process, demonstrate its efficacy in the presence of cells, and subsequently exploit it to induce subcellular detachment from soft hydrogels. A working space was established for a range of laser powers required to induce complete erosion of the gel, and these data are plotted with model predictions. From this working space, two-photon irradiation parameters were selected for complete erosion in the presence of cells. Micron-scale features were eroded on and within a gel to demonstrate the resolution of patterning with these irradiation conditions. Lastly, two-photon irradiation was used to erode the material at the cell-gel interface to remove cell adhesion sites selectively, and cell retraction was monitored to quantify the mesenchymal stem cell (MSC) response to subcellular detachment from soft materials.
细胞与细胞外基质(ECM)的黏附与脱离是细胞功能和命运的关键调节因素,这是因为细胞与其微环境之间会进行机械信号的交换。为了研究这种细胞力学生物学,研究人员开发了多种创新方法来体外研究细胞黏附;然而,这些培养平台大多质地异常坚硬或呈静态。为了更好地捕捉ECM柔软、动态的特性,我们展示了一种基于聚乙二醇(PEG)的水凝胶,其中细胞外空间的环境和几何形状可通过双光子诱导侵蚀在原位精确控制。在此,我们对双光子侵蚀过程进行了表征,证明了其在细胞存在时的有效性,随后利用它诱导细胞从柔软水凝胶上进行亚细胞脱离。针对诱导凝胶完全侵蚀所需的一系列激光功率建立了一个工作空间,并将这些数据与模型预测结果一起绘制。从这个工作空间中,选择了双光子照射参数以在细胞存在的情况下实现完全侵蚀。在凝胶表面及内部蚀刻微米级特征,以证明在这些照射条件下图案化的分辨率。最后,使用双光子照射来侵蚀细胞 - 凝胶界面处的材料,以选择性地去除细胞黏附位点,并监测细胞回缩以量化间充质干细胞(MSC)对从柔软材料上进行亚细胞脱离的反应。