3D-cultured blastoids model human embryogenesis from pre-implantation to early gastrulation stages

Our paper on extended human blastoid culture was published today in Cell Stem Cell. In a transformative advance, several groups have reported that naive human pluripotent stem cells (hPSCs) can form blastocyst-like structures (also known as “blastoids”) that model the human pre-implantation embryo. However, the extent to which blastoids can recapitulate defining features of post-implantation development remained unexplored. In this study, we optimized the conditions for blastoid generation from naïve hPSCs and investigated their capacity for extended culture on thick 3D extracellular matrices, which better mimic the physical environment of the human endometrium compared to flat surfaces. We developed an experimental methodology that supports human blastoid culture for up to day 21 (D21), including the formation of complex embryonic and placental structures. By performing a detailed single cell transcriptome analysis at three distinct time points (D7, D14, and D21), we benchmarked our model system to human embryos at pre-implantation, early post-implantation, and early gastrulation stages.

3D-cultured human blastoids display several molecular and morphogenetic hallmarks of early post-implantation development, including lumenogenesis of the epiblast compartment, rapid expansion and diversification of trophoblast lineages, and robust invasion of extravillous trophoblast cells by D14. Extended blastoid culture resulted in the formation of a primitive streak-like structure, as evidenced by the localized activation of TBXT (Brachyury) by D18. Blastoids maintained until D21 acquired a single cell transcriptome profile that closely resembled that of a gastrulating human embryo analyzed at Carnegie Stage 7. This included the emergence of blastoid primordial germ cells, definitive endoderm, and various mesodermal lineages, and a diverse array of extraembryonic cell types, including blastoid amnion, cytotrophoblast, extravillous trophoblast, extraembryonic mesoderm, syncytiotrophoblast, and yolk sac endoderm. Thus, the 3D-cultured human blastoids described herein model embryonic and extraembryonic development from pre-implantation to early gastrulation stages, offering a continuous and integrated in vitro model system of early embryogenesis.

Congratulations to Rowan, our collaborators in the Dietmann and Zhou labs, and the entire team!

Note: The generation of integrated models of human development in our laboratory is entirely supported by private foundation grants and does not involve federal funding from the National Institutes of Health.

A genome-wide CRISPR-Cas9 screen in human trophoblast stem cells

Our study describing a genome-wide CRISPR-Cas9 knockout screen for essential and growth-restricting genes in human trophoblast stem cells (hTSCs) was published in Nature Communications today. By cross-referencing our results to those from similar genetic screens performed in other cell types, as well as gene expression data from early human embryos, we define hTSC-specific and -enriched regulators. These include both well-established and previously uncharacterized trophoblast regulators. Integrated analysis of chromatin accessibility, gene expression, and genome-wide location data reveals that the hTSC-specific essential transcription factor TEAD1 regulates the expression of many trophoblast regulators in hTSCs. In the absence of TEAD1, hTSCs fail to complete faithful differentiation into extravillous trophoblast (EVT) cells and instead show a bias towards syncytiotrophoblast (STB) differentiation. Overall, our study provides a valuable resource for dissecting the molecular regulation of human placental development and pregnancy-related diseases. Congratulations to Chen Dong, who spearheaded this project in collaboration with Shuhua Fu in Bo Zhang’s lab at WashU, and all other contributors!

Paper on stem-cell-derived trophoblast organoids

Our paper on stem-cell-derived trophoblast organoids (SC-TOs) was published in Cell Stem Cell today. In this work we describe a methodology for deriving self-renewing 3D trophoblast organoids from naive human pluripotent stem cells (hPSCs). Using single cell transcriptome analysis, we demonstrate that these organoids contain diverse trophoblast progenitor and specialized cell types that closely correspond to trophoblast identities in the post-implantation embryo. These organoid cultures also model placental X inactivation dynamics and selective vulnerability to emerging pathogens (SARS-CoV-2 and Zika virus). Big congrats to all members of the team, especially Rowan Karvas, and our collaborators Indira Mysorekar, Sabine Dietmann, Jacco Boon, and Liang Ma!