Park Joong Yull, Morgan Mina, Sachs Aaron N, Samorezov Julia, Teller Ryan, Shen Ye, Pienta Kenneth J, Takayama Shuichi
Department of Biomedical Engineering, College of Engineering, University of Michigan, 2200 Bonisteel Blvd, Ann Arbor, MI 48109, USA.
Microfluid Nanofluidics. 2010 Feb 1;8(2):263-268. doi: 10.1007/s10404-009-0503-9.
Conventional cell trapping methods using microwells with small dimensions (10-20 μm) are useful for examining the instantaneous cell response to reagents; however, such wells have insufficient space for longer duration screening tests that require observation of cell attachment and division. Here we describe a flow method that enables single cell trapping in microwells with dimensions of 50 μm, a size sufficient to allow attachment and division of captured cells. Among various geometries tested, triangular microwells were found to be most efficient for single cell trapping while providing ample space for cells to grow and spread. An important trapping mechanism is the formation of fluid streamlines inside, rather than over, the microwells. A strong flow recirculation occurs in the triangular microwell so that it efficiently catches cells. Once a cell is captured, the cell presence in the microwell changes the flow pattern, thereby preventing trapping of other cells. About 62% of microwells were filled with single cells after a 20 min loading procedure. Human prostate cancer cells (PC3) were used for validation of our system.
使用小尺寸(10 - 20μm)微孔的传统细胞捕获方法对于检测细胞对试剂的即时反应很有用;然而,对于需要观察细胞附着和分裂的较长时间筛选测试而言,此类微孔的空间不足。在此,我们描述了一种流动方法,该方法能够在尺寸为50μm的微孔中捕获单个细胞,此尺寸足以让捕获的细胞附着和分裂。在测试的各种几何形状中,发现三角形微孔对于单个细胞捕获最为有效,同时为细胞生长和铺展提供了充足空间。一个重要的捕获机制是在微孔内部而非上方形成流体流线。在三角形微孔中会发生强烈的流动再循环,从而有效地捕获细胞。一旦捕获一个细胞,微孔中细胞的存在会改变流动模式,进而阻止其他细胞的捕获。经过20分钟的加载过程后,约62%的微孔中填充了单个细胞。使用人前列腺癌细胞(PC3)对我们的系统进行验证。