诱导多能干细胞
类有机物
细胞保护
细胞生物学
胚胎干细胞
生物
干细胞
细胞分化
定向微分
重编程
细胞
计算生物学
遗传学
细胞凋亡
基因
作者
Yu Chen,Carlos A. Tristan,Lu Chen,Vukasin M. Jovanovic,Claire Malley,Pei‐Hsuan Chu,Seungmi Ryu,Tao Deng,Pinar Ormanoglu,Dingyin Tao,Yuhong Fang,Jaroslav Slamecka,Hyenjong Hong,Christopher A. LeClair,Sam Michael,Christopher P. Austin,Anton Simeonov,Ilyas Singeç
出处
期刊:Nature Methods
[Springer Nature]
日期:2021-05-01
卷期号:18 (5): 528-541
被引量:99
标识
DOI:10.1038/s41592-021-01126-2
摘要
Human pluripotent stem cells (hPSCs) are capable of extensive self-renewal yet remain highly sensitive to environmental perturbations in vitro, posing challenges to their therapeutic use. There is an urgent need to advance strategies that ensure safe and robust long-term growth and functional differentiation of these cells. Here, we deployed high-throughput screening strategies to identify a small-molecule cocktail that improves viability of hPSCs and their differentiated progeny. The combination of chroman 1, emricasan, polyamines, and trans-ISRIB (CEPT) enhanced cell survival of genetically stable hPSCs by simultaneously blocking several stress mechanisms that otherwise compromise cell structure and function. CEPT provided strong improvements for several key applications in stem-cell research, including routine cell passaging, cryopreservation of pluripotent and differentiated cells, embryoid body (EB) and organoid formation, single-cell cloning, and genome editing. Thus, CEPT represents a unique poly-pharmacological strategy for comprehensive cytoprotection, providing a rationale for efficient and safe utilization of hPSCs. The CEPT cocktail comprising four small molecules enhances pluripotent stem cell survival, biobanking, organoid formation, and single-cell cloning efficiency by reducing cellular stress.
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