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Self-patterning of rostral-caudal neuroectoderm requires dual role of Fgf signaling for localized Wnt antagonism

The neuroectoderm is patterned along a rostral-caudal axis in response to localized factors in the embryo, but exactly how these factors act as positional information for this patterning is not yet fully understood. Here, using the self-organizing properties of mouse embryonic stem cell (ESC), we re...

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Autores principales: Takata, Nozomu, Sakakura, Eriko, Eiraku, Mototsugu, Kasukawa, Takeya, Sasai, Yoshiki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5673904/
https://www.ncbi.nlm.nih.gov/pubmed/29109536
http://dx.doi.org/10.1038/s41467-017-01105-2
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author Takata, Nozomu
Sakakura, Eriko
Eiraku, Mototsugu
Kasukawa, Takeya
Sasai, Yoshiki
author_facet Takata, Nozomu
Sakakura, Eriko
Eiraku, Mototsugu
Kasukawa, Takeya
Sasai, Yoshiki
author_sort Takata, Nozomu
collection PubMed
description The neuroectoderm is patterned along a rostral-caudal axis in response to localized factors in the embryo, but exactly how these factors act as positional information for this patterning is not yet fully understood. Here, using the self-organizing properties of mouse embryonic stem cell (ESC), we report that ESC-derived neuroectoderm self-generates a Six3(+) rostral and a Irx3(+) caudal bipolarized patterning. In this instance, localized Fgf signaling performs dual roles, as it regulates Six3(+) rostral polarization at an earlier stage and promotes Wnt signaling at a later stage. The Wnt signaling components are differentially expressed in the polarized tissues, leading to genome-wide Irx3(+) caudal-polarization signals. Surprisingly, differentially expressed Wnt agonists and antagonists have essential roles in orchestrating the formation of a balanced rostral-caudal neuroectoderm pattern. Together, our findings provide key processes for dynamic self-patterning and evidence that a temporally and locally regulated interaction between Fgf and Wnt signaling controls self-patterning in ESC-derived neuroectoderm.
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spelling pubmed-56739042017-11-09 Self-patterning of rostral-caudal neuroectoderm requires dual role of Fgf signaling for localized Wnt antagonism Takata, Nozomu Sakakura, Eriko Eiraku, Mototsugu Kasukawa, Takeya Sasai, Yoshiki Nat Commun Article The neuroectoderm is patterned along a rostral-caudal axis in response to localized factors in the embryo, but exactly how these factors act as positional information for this patterning is not yet fully understood. Here, using the self-organizing properties of mouse embryonic stem cell (ESC), we report that ESC-derived neuroectoderm self-generates a Six3(+) rostral and a Irx3(+) caudal bipolarized patterning. In this instance, localized Fgf signaling performs dual roles, as it regulates Six3(+) rostral polarization at an earlier stage and promotes Wnt signaling at a later stage. The Wnt signaling components are differentially expressed in the polarized tissues, leading to genome-wide Irx3(+) caudal-polarization signals. Surprisingly, differentially expressed Wnt agonists and antagonists have essential roles in orchestrating the formation of a balanced rostral-caudal neuroectoderm pattern. Together, our findings provide key processes for dynamic self-patterning and evidence that a temporally and locally regulated interaction between Fgf and Wnt signaling controls self-patterning in ESC-derived neuroectoderm. Nature Publishing Group UK 2017-11-07 /pmc/articles/PMC5673904/ /pubmed/29109536 http://dx.doi.org/10.1038/s41467-017-01105-2 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Takata, Nozomu
Sakakura, Eriko
Eiraku, Mototsugu
Kasukawa, Takeya
Sasai, Yoshiki
Self-patterning of rostral-caudal neuroectoderm requires dual role of Fgf signaling for localized Wnt antagonism
title Self-patterning of rostral-caudal neuroectoderm requires dual role of Fgf signaling for localized Wnt antagonism
title_full Self-patterning of rostral-caudal neuroectoderm requires dual role of Fgf signaling for localized Wnt antagonism
title_fullStr Self-patterning of rostral-caudal neuroectoderm requires dual role of Fgf signaling for localized Wnt antagonism
title_full_unstemmed Self-patterning of rostral-caudal neuroectoderm requires dual role of Fgf signaling for localized Wnt antagonism
title_short Self-patterning of rostral-caudal neuroectoderm requires dual role of Fgf signaling for localized Wnt antagonism
title_sort self-patterning of rostral-caudal neuroectoderm requires dual role of fgf signaling for localized wnt antagonism
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5673904/
https://www.ncbi.nlm.nih.gov/pubmed/29109536
http://dx.doi.org/10.1038/s41467-017-01105-2
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