Defining the Teratoma as a Model for Multi-lineage Human Development
Author(s) -
Daniella McDonald,
Yan Wu,
Amir Dailamy,
Justin Tat,
Udit Parekh,
Dongxin Zhao,
Michael Hu,
Ann Tipps,
Kun Zhang,
Prashant Mali
Publication year - 2020
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2020.10.018
Subject(s) - biology , teratoma , cell type , crispr , lineage (genetic) , germ layer , embryonic stem cell , germ cell , stem cell , microrna , computational biology , microbiology and biotechnology , cell , gene , organoid , genetics , induced pluripotent stem cell , pathology , medicine
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 multi-lineage development, pan-tissue functional genetic screening, and tissue engineering.
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