Literature DB >> 33152263

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

Daniella McDonald1, Yan Wu2, Amir Dailamy2, Justin Tat3, Udit Parekh4, Dongxin Zhao2, Michael Hu2, Ann Tipps5, Kun Zhang6, Prashant Mali7.   

Abstract

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.
Copyright © 2020 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  CRISPR-Cas9; barcoding; genetic circuits; genetic screens; miRNAs; model systems; multi-lineage development; single-cell RNA sequencing; teratoma; tissue engineering

Mesh:

Substances:

Year:  2020        PMID: 33152263      PMCID: PMC7704916          DOI: 10.1016/j.cell.2020.10.018

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


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