BioMEMS Resource Center, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts, USA.
Biophys J. 2012 Feb 22;102(4):721-30. doi: 10.1016/j.bpj.2011.12.044. Epub 2012 Feb 21.
Adhesion-based cell capture on surfaces in microfluidic devices forms the basis of numerous biomedical diagnostics and in vitro assays. However, the performance of these platforms is partly limited by interfacial phenomena that occur at low Reynolds numbers. In contrast, cell homing to porous vasculature is highly effective in vivo during inflammation, stem cell trafficking, and cancer metastasis. Here, we show that a porous, fluid-permeable surface functionalized with cell-specific antibodies promotes efficient and selective cell capture in vitro. This architecture is advantageous due to enhanced transport as streamlines are diverted toward the surface. Moreover, specific cell-surface interactions are promoted due to reduced shear, allowing gentle cell rolling and arrest. Together, these synergistic effects enable highly effective cell capture at flow rates more than an order of magnitude larger than those provided by existing devices with solid surfaces.
基于黏附的细胞在微流控设备表面的捕获是许多生物医学诊断和体外分析的基础。然而,这些平台的性能在一定程度上受到低雷诺数下发生的界面现象的限制。相比之下,在炎症、干细胞迁移和癌症转移过程中,细胞归巢到多孔血管是非常有效的。在这里,我们表明,用细胞特异性抗体功能化的多孔、可渗透流体的表面促进了体外高效和选择性的细胞捕获。由于流线被分流到表面,这种结构具有优势。此外,由于剪切力降低,促进了特定的细胞-表面相互作用,从而允许细胞轻柔地滚动和停止。这些协同效应使得在比具有固体表面的现有设备提供的流速大一个数量级以上的流速下,能够实现高效的细胞捕获。