Remple Krissy, Stone Laurel
Department of Molecular and Cell Biology, Life Technologies.
J Vis Exp. 2011 Nov 17(57):3659. doi: 10.3791/3659.
Single-cell and population information are commonly obtained either by flow cytometry or fluorescence microscopy. However, these two methods provide different information. Flow cytometry gives quantitative multi-parametric information about physical characteristics and staining or expression, but doesn't allow for visualization. Stand-alone fluorescence microscopy provides visual data, but doesn't allow for straightforward quantitative measurements(1). Image-based cytometry bridges the gap between these two methods, enabling the quick visualization and simultaneous quantitative analysis of thousands of cells in heterogeneous populations(2). Here, we present a method for performing cell viability and green fluorescent protein (GFP) expression assays using the Tali Image-Based Cytometer(3). The Tali instrument is a 3-channel (bright field, green fluorescence, red fluorescence) benchtop assay platform that offers several advantages over flow cytometry and fluorescence microscopy. The Tali cytometer is less expensive, takes up less bench space, requires less maintenance, and the work flow has been simplified so that the operation and analysis is much simpler and quicker. The Tali cytometer is capable of performing a range of suspension cell-based assays, including GFP and red fluorescent protein (RFP) expression, apoptosis(4-6) and cell viability analysis with propidium iodide (PI)(7-11). Here, we demonstrate the use of the Tali instrument in performing a cell viability assay in cells expressing GFP. GFP-transduced cells are stained using the Tali Viability Kit - Dead Cell Red. The cells are then pipetted into a Tali Cellular Analysis Slide and loaded into the cytometer. Bright field, red fluorescence and green fluorescence images are captured and analyzed using assay specific algorithms. Histograms are then generated to display cell size, PI fluorescence intensity, and GFP fluorescence intensity. These parameters can then be thresholded to home in on a specific cell population. A side-by side comparison of the Tali Image-Based Cytometer and traditional flow cytometry demonstrates that the two methods provide comparable data regarding cell viability and protein expression. However, the Tali instrument provides additional visual information about the cell population that cannot be obtained using a flow cytometer.
单细胞和群体信息通常通过流式细胞术或荧光显微镜获得。然而,这两种方法提供的信息不同。流式细胞术可提供有关物理特征以及染色或表达的定量多参数信息,但无法进行可视化观察。单独的荧光显微镜可提供视觉数据,但无法进行直接的定量测量(1)。基于图像的细胞术弥补了这两种方法之间的差距,能够对异质群体中的数千个细胞进行快速可视化和同步定量分析(2)。在此,我们介绍一种使用Tali基于图像的细胞仪进行细胞活力和绿色荧光蛋白(GFP)表达检测的方法(3)。Tali仪器是一个三通道(明场、绿色荧光、红色荧光)台式检测平台,与流式细胞术和荧光显微镜相比具有多个优势。Tali细胞仪价格更低,占用台面空间更小,维护需求更少,并且工作流程得到简化,因此操作和分析更加简单快捷。Tali细胞仪能够进行一系列基于悬浮细胞的检测,包括GFP和红色荧光蛋白(RFP)表达、凋亡(4 - 6)以及使用碘化丙啶(PI)进行细胞活力分析(7 - 11)。在此,我们展示了Tali仪器在对表达GFP的细胞进行细胞活力检测中的应用。使用Tali活力试剂盒 - 死细胞红对GFP转导的细胞进行染色。然后将细胞吸移到Tali细胞分析载玻片上并加载到细胞仪中。使用特定检测算法捕获并分析明场、红色荧光和绿色荧光图像。随后生成直方图以显示细胞大小、PI荧光强度和GFP荧光强度。然后可以对这些参数进行阈值设定,以聚焦于特定细胞群体。对Tali基于图像的细胞仪和传统流式细胞术的并排比较表明,这两种方法在细胞活力和蛋白质表达方面提供了可比的数据。然而,Tali仪器提供了使用流式细胞仪无法获得的有关细胞群体的额外视觉信息。