Duchamp Margaux, Dahoun Thamani, Vaillier Clarisse, Arnaud Marion, Bobisse Sara, Coukos George, Harari Alexandre, Renaud Philippe
Laboratory of Microsystems LMIS4, Ecole Polytechnique Fédérale de Lausanne (EPFL) Lausanne Switzerland
Department of Oncology, Lausanne University Hospital, Ludwig Institute for Cancer Research, University of Lausanne Lausanne CH-1066 Switzerland.
RSC Adv. 2019 Dec 13;9(70):41066-41073. doi: 10.1039/c9ra09504g. eCollection 2019 Dec 9.
In this study we present a novel microfluidic hydrodynamic trapping device to probe the cell-cell interaction between all cell samples of two distinct populations. We have exploited an hydrodynamic trapping method using microfluidics to immobilize a batch of cells from the first population at specific locations, then relied on hydrodynamic filtering principles, the flowing cells from the second cell population are placed in contact with the trapped ones, through a roll-over mechanism. The rolling cells interact with the serially trapped cells one after the other. The proposed microfluidic phenomenon was characterized with beads. We have shown the validity of our method by detecting the capacity of olfactory receptors to induce adhesion of cell doublets overexpressing these receptors. We report here the first controlled on-flow single cell resolution cell-cell interaction assay in a microfluidic device for future application in cell-cell interactions-based cell library screenings.
在本研究中,我们展示了一种新型的微流控流体动力学捕获装置,用于探究两个不同群体的所有细胞样本之间的细胞间相互作用。我们利用一种基于微流控的流体动力学捕获方法,将第一批群体的一批细胞固定在特定位置,然后依靠流体动力学过滤原理,通过翻转机制使来自第二批细胞群体的流动细胞与捕获的细胞接触。滚动的细胞依次与连续捕获的细胞相互作用。所提出的微流控现象用珠子进行了表征。我们通过检测嗅觉受体诱导过表达这些受体的细胞双联体黏附的能力,证明了我们方法的有效性。我们在此报告了在微流控装置中首次实现的可控的、基于流动的单细胞分辨率细胞间相互作用分析,以供未来在基于细胞间相互作用的细胞文库筛选中应用。