Yang Bin, Kuang Junqi, Wu Chuman, Zhou Wenyi, Zhu Shuoji, Jiang Haodong, Zhai Ziwei, Wu Yue, Peng Junwei, Liu Nanbo, Hu Haiyan, Ide Nasser Moussa, Chen Ruiping, Zhao Mingyi, Zhu Ping
The Second School of Clinical Medicine, Southern Medical University, Guangzhou, Guangdong 510515, China.
Guangdong Institute of Cardiovascular Disease, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Guangzhou, Guangdong 510080, China.
Stem Cells Int. 2020 Feb 3;2020:8483035. doi: 10.1155/2020/8483035. eCollection 2020.
Two of the main problems of stem cell and regenerative medicine are the exit of pluripotency and differentiation to functional cells or tissues. The answer to these two problems holds great value in the clinical translation of stem cell as well as regenerative medicine research. Although piling researches have revealed the truth about pluripotency maintenance, the mechanisms underlying pluripotent cell self-renewal, proliferation, and differentiation into specific cell lineages or tissues are yet to be defined. To this end, we took full advantage of a novel technology, namely, the genome-scale CRISPR-Cas9 knockout (GeCKO). As an effective way of introducing targeted loss-of-function mutations at specific sites in the genome, GeCKO is able to screen in an unbiased manner for key genes that promote exit from pluripotency in mouse embryonic stem cells (mESCs) for the first time. In this study, we successfully established a model based on GeCKO to screen the key genes in pluripotency withdrawal. Our strategies included lentiviral package and infection technology, lenti-Cas9 gene knockout technology, shRNA gene knockdown technology, next-generation sequencing, model-based analysis of genome-scale CRISPR-Cas9 knockout (MAGeCK analysis), GO analysis, and other methods. Our findings provide a novel approach for large-scale screening of genes involved in pluripotency exit and offer an entry point for cell fate regulation research.
干细胞与再生医学的两个主要问题是多能性的退出以及向功能细胞或组织的分化。解决这两个问题对于干细胞临床转化以及再生医学研究具有重要价值。尽管大量研究揭示了多能性维持的真相,但多能细胞自我更新、增殖以及分化为特定细胞谱系或组织的潜在机制仍有待明确。为此,我们充分利用了一项新技术,即基因组规模的CRISPR-Cas9基因敲除(GeCKO)。作为在基因组特定位点引入靶向功能丧失突变的有效方法,GeCKO首次能够以无偏倚的方式筛选促进小鼠胚胎干细胞(mESCs)多能性退出的关键基因。在本研究中,我们成功建立了基于GeCKO的模型来筛选多能性退出中的关键基因。我们的策略包括慢病毒包装与感染技术、慢病毒Cas9基因敲除技术、shRNA基因敲低技术、下一代测序、基于模型的基因组规模CRISPR-Cas9基因敲除分析(MAGeCK分析)、GO分析以及其他方法。我们的研究结果为大规模筛选参与多能性退出的基因提供了一种新方法,并为细胞命运调控研究提供了一个切入点。