Defining the Teratoma as a Model for Multi-lineage Human Development

被引:31
|
作者
McDonald, Daniella [1 ,2 ]
Wu, Yan [1 ]
Dailamy, Amir [1 ]
Tat, Justin [3 ]
Parekh, Udit [5 ]
Zhao, Dongxin [1 ]
Hu, Michael [1 ]
Tipps, Ann [4 ]
Zhang, Kun [1 ,2 ]
Mali, Prashant [1 ,2 ]
机构
[1] Univ Calif San Diego, Dept Bioengn, San Diego, CA 92093 USA
[2] Univ Calif San Diego, Biomed Sci Grad Program, San Diego, CA 92093 USA
[3] Univ Calif San Diego, Dept Biol Sci, San Diego, CA 92093 USA
[4] Univ Calif San Diego, Sch Med, San Diego, CA 92103 USA
[5] Univ Calif San Diego, Dept Elect & Comp Engn, San Diego, CA 92093 USA
关键词
HEMATOPOIETIC STEM-CELLS; GENE-EXPRESSION; IN-VITRO; DISEASE; MOUSE; MICRORNA-21; ORGANOIDS; CANCER; CRISPR; BRAIN;
D O I
10.1016/j.cell.2020.10.018
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We propose that the teratoma, a recognized standard for validating pluripotency in stem cells, could be a promising platform for studying human developmental processes. Performing single-cell RNA sequencing (RNA-seq) of 179,632 cells across 23 teratomas from 4 cell lines, we found that teratomas reproducibly contain approximately 20 cell types across all 3 germ layers, that inter-teratoma cell type heterogeneity is comparable with organoid systems, and teratoma gut and brain cell types correspond well to similar fetal cell types. Furthermore, cellular barcoding confirmed that injected stem cells robustly engraft and contribute to all lineages. Using pooled CRISPR-Cas9 knockout screens, we showed that teratomas can enable simultaneous assaying of the effects of genetic perturbations across all germ layers. Additionally, we demonstrated that teratomas can be sculpted molecularly via microRNA (miRNA)-regulated suicide gene expression to enrich for specific tissues. Taken together, teratomas are a promising platform for modeling multilineage development, pan-tissue functional genetic screening, and tissue engineering.
引用
收藏
页码:1402 / +
页数:36
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