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Mechanisms of human embryo development: from cell fate to tissue shape and back

Gene regulatory networks and tissue morphogenetic events drive the emergence of shape and function: the pillars of embryo development. Although model systems offer a window into the molecular biology of cell fate and tissue shape, mechanistic studies of our own development have so far been technical...

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Autor principal: Shahbazi, Marta N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7375473/
https://www.ncbi.nlm.nih.gov/pubmed/32680920
http://dx.doi.org/10.1242/dev.190629
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author Shahbazi, Marta N.
author_facet Shahbazi, Marta N.
author_sort Shahbazi, Marta N.
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description Gene regulatory networks and tissue morphogenetic events drive the emergence of shape and function: the pillars of embryo development. Although model systems offer a window into the molecular biology of cell fate and tissue shape, mechanistic studies of our own development have so far been technically and ethically challenging. However, recent technical developments provide the tools to describe, manipulate and mimic human embryos in a dish, thus opening a new avenue to exploring human development. Here, I discuss the evidence that supports a role for the crosstalk between cell fate and tissue shape during early human embryogenesis. This is a critical developmental period, when the body plan is laid out and many pregnancies fail. Dissecting the basic mechanisms that coordinate cell fate and tissue shape will generate an integrated understanding of early embryogenesis and new strategies for therapeutic intervention in early pregnancy loss.
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spelling pubmed-73754732020-07-30 Mechanisms of human embryo development: from cell fate to tissue shape and back Shahbazi, Marta N. Development Review Gene regulatory networks and tissue morphogenetic events drive the emergence of shape and function: the pillars of embryo development. Although model systems offer a window into the molecular biology of cell fate and tissue shape, mechanistic studies of our own development have so far been technically and ethically challenging. However, recent technical developments provide the tools to describe, manipulate and mimic human embryos in a dish, thus opening a new avenue to exploring human development. Here, I discuss the evidence that supports a role for the crosstalk between cell fate and tissue shape during early human embryogenesis. This is a critical developmental period, when the body plan is laid out and many pregnancies fail. Dissecting the basic mechanisms that coordinate cell fate and tissue shape will generate an integrated understanding of early embryogenesis and new strategies for therapeutic intervention in early pregnancy loss. The Company of Biologists Ltd 2020-07-17 /pmc/articles/PMC7375473/ /pubmed/32680920 http://dx.doi.org/10.1242/dev.190629 Text en © 2020. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/4.0This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Review
Shahbazi, Marta N.
Mechanisms of human embryo development: from cell fate to tissue shape and back
title Mechanisms of human embryo development: from cell fate to tissue shape and back
title_full Mechanisms of human embryo development: from cell fate to tissue shape and back
title_fullStr Mechanisms of human embryo development: from cell fate to tissue shape and back
title_full_unstemmed Mechanisms of human embryo development: from cell fate to tissue shape and back
title_short Mechanisms of human embryo development: from cell fate to tissue shape and back
title_sort mechanisms of human embryo development: from cell fate to tissue shape and back
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7375473/
https://www.ncbi.nlm.nih.gov/pubmed/32680920
http://dx.doi.org/10.1242/dev.190629
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