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自动化单细胞分离和人多能干细胞亚克隆的方法。

Methods for Automated Single Cell Isolation and Sub-Cloning of Human Pluripotent Stem Cells.

机构信息

Charité-Universitätsmedizin Berlin, Berlin, Germany.

Berlin Institute of Health (BIH), BIH Stem Cell Core Facility, Berlin, Germany.

出版信息

Curr Protoc Stem Cell Biol. 2020 Dec;55(1):e123. doi: 10.1002/cpsc.123.

Abstract

Advances in human pluripotent stem cell (hPSC) techniques have led them to become a widely used and powerful tool for a vast array of applications, including disease modeling, developmental studies, drug discovery and testing, and emerging cell-based therapies. hPSC workflows that require clonal expansion from single cells, such as CRISPR/Cas9-mediated genome editing, face major challenges in terms of efficiency, cost, and precision. Classical sub-cloning approaches depend on limiting dilution and manual colony picking, which are both time-consuming and labor-intensive, and lack a real proof of clonality. Here we describe the application of three different automated cell isolation and dispensing devices that can enhance the single-cell cloning process for hPSCs. In combination with optimized cell culture conditions, these devices offer an attractive alternative compared to manual methods. We explore various aspects of each device system and define protocols for their practical application. Following the workflow described here, single cell-derived hPSC sub-clones from each system maintain pluripotency and genetic stability. Furthermore, the workflows can be applied to uncover karyotypic mosaicism prevalent in bulk hPSC cultures. Our robust automated workflow facilitates high-throughput hPSC clonal selection and expansion, urgently needed in the operational pipelines of hPSC applications. © 2020 The Authors. Basic Protocol: Efficient automated hPSC single cell seeding and clonal expansion using the iotaSciences IsoCell platform Alternate Protocol 1: hPSC single cell seeding and clonal expansion using the Cellenion CellenONE single-cell dispenser Alternate Protocol 2: hPSC single cell seeding and clonal expansion using the Cytena single-cell dispenser Support Protocol 1: Coating cell culture plates with Geltrex Support Protocol 2: hPSC maintenance in defined feeder-free conditions Support Protocol 3: hPSC passaging in clumps Support Protocol 4: Laminin 521 coating of IsoCell plates and 96-well/384-well plates Support Protocol 5: Preparation of medium containing anti-apoptotic small molecules Support Protocol 6: 96- and 384-well target plate preparation prior to single cell seeding Support Protocol 7: Single cell dissociation of hPSCs Support Protocol 8: IsoCell-, CellenONE-, and Cytena-derived hPSC clone subculture and expansion.

摘要

人类多能干细胞(hPSC)技术的进步使其成为广泛应用和强大的工具,可用于各种应用,包括疾病建模、发育研究、药物发现和测试以及新兴的基于细胞的治疗。需要从单细胞进行克隆扩增的 hPSC 工作流程,例如 CRISPR/Cas9 介导的基因组编辑,在效率、成本和精度方面面临重大挑战。经典的亚克隆方法依赖于有限稀释和手动集落挑选,这两种方法既耗时又费力,并且缺乏真正的克隆证明。在这里,我们描述了三种不同的自动化细胞分离和分配设备的应用,这些设备可以增强 hPSC 的单细胞克隆过程。与手动方法相比,结合优化的细胞培养条件,这些设备提供了一种有吸引力的替代方案。我们探索了每个设备系统的各个方面,并为其实际应用定义了协议。按照这里描述的工作流程,来自每个系统的单细胞衍生的 hPSC 亚克隆保持多能性和遗传稳定性。此外,该工作流程可应用于揭示大量 hPSC 培养物中普遍存在的核型嵌合体。我们强大的自动化工作流程促进了高通量 hPSC 克隆选择和扩增,这在 hPSC 应用的操作管道中是迫切需要的。© 2020 作者。基本方案:使用 iotaSciences IsoCell 平台高效自动化 hPSC 单细胞播种和克隆扩增备选方案 1:使用 Cellenion CellenONE 单细胞分配器进行 hPSC 单细胞播种和克隆扩增备选方案 2:使用 Cytena 单细胞分配器进行 hPSC 单细胞播种和克隆扩增支持方案 1:用 Geltrex 涂覆细胞培养板支持方案 2:无饲养层条件下 hPSC 的维持支持方案 3:hPSC 团块传代支持方案 4:IsoCell 板和 96 孔/384 孔板的层粘连蛋白 521 涂层支持方案 5:制备含有抗凋亡小分子的培养基支持方案 6:单细胞播种前 96 孔和 384 孔靶板的准备支持方案 7:hPSC 的单细胞解离支持方案 8:IsoCell、CellenONE 和 Cytena 衍生的 hPSC 克隆亚培养和扩增。

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