Chien Miao-Ping, Werley Christopher A, Farhi Samouil L, Cohen Adam E
Departments of Chemistry and Chemical Biology and Physics, Harvard Stem Cell Institute, Harvard University, Cambridge, MA 02138 Howard Hughes Medical Institute.
Chem Sci. 2015 Mar;6(3):1701-1705. doi: 10.1039/C4SC03676J.
Sorting of target cells from a heterogeneous pool is technically difficult when the selection criterion is complex, e.g. a dynamic response, a morphological feature, or a combination of multiple parameters. At present, mammalian cell selections are typically performed either via static fluorescence (e.g. fluorescence activated cell sorter), via survival (e.g. antibiotic resistance), or via serial operations (flow cytometry, laser capture microdissection). Here we present a simple protocol for selecting cells based on any static or dynamic property that can be identified by video microscopy and image processing. The "photostick" technique uses a cell-impermeant photochemical crosslinker and digital micromirror array-based patterned illumination to immobilize selected cells on the culture dish. Other cells are washed away with mild protease treatment. The crosslinker also labels the selected cells with a fluorescent dye and a biotin for later identification. The photostick protocol preserves cell viability, permits genetic profiling of selected cells, and can be performed with complex functional selection criteria such as neuronal firing patterns.
当选择标准较为复杂时,比如动态反应、形态特征或多个参数的组合,从异质细胞群中筛选目标细胞在技术上具有挑战性。目前,哺乳动物细胞的筛选通常通过静态荧光(如荧光激活细胞分选仪)、通过存活能力(如抗生素抗性)或通过系列操作(流式细胞术、激光捕获显微切割)来进行。在此,我们提出一种简单的方案,用于基于任何可通过视频显微镜和图像处理识别的静态或动态特性来筛选细胞。“光棒”技术使用一种细胞不可渗透的光化学交联剂和基于数字微镜阵列的图案化照明,将选定的细胞固定在培养皿上。通过温和的蛋白酶处理将其他细胞洗去。交联剂还用荧光染料和生物素标记选定的细胞,以便后续识别。光棒方案可保持细胞活力,允许对选定细胞进行基因分析,并且可以根据复杂的功能选择标准(如神经元放电模式)来执行。