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High-resolution transcriptional and morphogenetic profiling of cells from micropatterned human ESC gastruloid cultures
During mammalian gastrulation, germ layers arise and are shaped into the body plan while extraembryonic layers sustain the embryo. Human embryonic stem cells, cultured with BMP4 on extracellular matrix micro-discs, reproducibly differentiate into gastruloids, expressing markers of germ layers and ex...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7728446/ https://www.ncbi.nlm.nih.gov/pubmed/33206048 http://dx.doi.org/10.7554/eLife.59445 |
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author | Minn, Kyaw Thu Fu, Yuheng C He, Shenghua Dietmann, Sabine George, Steven C Anastasio, Mark A Morris, Samantha A Solnica-Krezel, Lilianna |
author_facet | Minn, Kyaw Thu Fu, Yuheng C He, Shenghua Dietmann, Sabine George, Steven C Anastasio, Mark A Morris, Samantha A Solnica-Krezel, Lilianna |
author_sort | Minn, Kyaw Thu |
collection | PubMed |
description | During mammalian gastrulation, germ layers arise and are shaped into the body plan while extraembryonic layers sustain the embryo. Human embryonic stem cells, cultured with BMP4 on extracellular matrix micro-discs, reproducibly differentiate into gastruloids, expressing markers of germ layers and extraembryonic cells in radial arrangement. Using single-cell RNA sequencing and cross-species comparisons with mouse, cynomolgus monkey gastrulae, and post-implantation human embryos, we reveal that gastruloids contain cells transcriptionally similar to epiblast, ectoderm, mesoderm, endoderm, primordial germ cells, trophectoderm, and amnion. Upon gastruloid dissociation, single cells reseeded onto micro-discs were motile and aggregated with the same but segregated from distinct cell types. Ectodermal cells segregated from endodermal and extraembryonic but mixed with mesodermal cells. Our work demonstrates that the gastruloid system models primate-specific features of embryogenesis, and that gastruloid cells exhibit evolutionarily conserved sorting behaviors. This work generates a resource for transcriptomes of human extraembryonic and embryonic germ layers differentiated in a stereotyped arrangement. |
format | Online Article Text |
id | pubmed-7728446 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-77284462020-12-14 High-resolution transcriptional and morphogenetic profiling of cells from micropatterned human ESC gastruloid cultures Minn, Kyaw Thu Fu, Yuheng C He, Shenghua Dietmann, Sabine George, Steven C Anastasio, Mark A Morris, Samantha A Solnica-Krezel, Lilianna eLife Developmental Biology During mammalian gastrulation, germ layers arise and are shaped into the body plan while extraembryonic layers sustain the embryo. Human embryonic stem cells, cultured with BMP4 on extracellular matrix micro-discs, reproducibly differentiate into gastruloids, expressing markers of germ layers and extraembryonic cells in radial arrangement. Using single-cell RNA sequencing and cross-species comparisons with mouse, cynomolgus monkey gastrulae, and post-implantation human embryos, we reveal that gastruloids contain cells transcriptionally similar to epiblast, ectoderm, mesoderm, endoderm, primordial germ cells, trophectoderm, and amnion. Upon gastruloid dissociation, single cells reseeded onto micro-discs were motile and aggregated with the same but segregated from distinct cell types. Ectodermal cells segregated from endodermal and extraembryonic but mixed with mesodermal cells. Our work demonstrates that the gastruloid system models primate-specific features of embryogenesis, and that gastruloid cells exhibit evolutionarily conserved sorting behaviors. This work generates a resource for transcriptomes of human extraembryonic and embryonic germ layers differentiated in a stereotyped arrangement. eLife Sciences Publications, Ltd 2020-11-18 /pmc/articles/PMC7728446/ /pubmed/33206048 http://dx.doi.org/10.7554/eLife.59445 Text en © 2020, Minn et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Developmental Biology Minn, Kyaw Thu Fu, Yuheng C He, Shenghua Dietmann, Sabine George, Steven C Anastasio, Mark A Morris, Samantha A Solnica-Krezel, Lilianna High-resolution transcriptional and morphogenetic profiling of cells from micropatterned human ESC gastruloid cultures |
title | High-resolution transcriptional and morphogenetic profiling of cells from micropatterned human ESC gastruloid cultures |
title_full | High-resolution transcriptional and morphogenetic profiling of cells from micropatterned human ESC gastruloid cultures |
title_fullStr | High-resolution transcriptional and morphogenetic profiling of cells from micropatterned human ESC gastruloid cultures |
title_full_unstemmed | High-resolution transcriptional and morphogenetic profiling of cells from micropatterned human ESC gastruloid cultures |
title_short | High-resolution transcriptional and morphogenetic profiling of cells from micropatterned human ESC gastruloid cultures |
title_sort | high-resolution transcriptional and morphogenetic profiling of cells from micropatterned human esc gastruloid cultures |
topic | Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7728446/ https://www.ncbi.nlm.nih.gov/pubmed/33206048 http://dx.doi.org/10.7554/eLife.59445 |
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