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Anteroposterior Wnt-RA Gradient Defines Adhesion and Migration Properties of Neural Progenitors in Developing Spinal Cord
Mammalian embryos exhibit a transition from head morphogenesis to trunk elongation to meet the demand of axial elongation. The caudal neural tube (NT) is formed with neural progenitors (NPCs) derived from neuromesodermal progenitors localized at the tail tip. However, the molecular and cellular basi...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7562945/ https://www.ncbi.nlm.nih.gov/pubmed/32976767 http://dx.doi.org/10.1016/j.stemcr.2020.08.016 |
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author | Shaker, Mohammed R. Lee, Ju-Hyun Park, Si-Hyung Kim, Joo Yeon Son, Gi Hoon Son, Jong Wan Park, Bae Ho Rhyu, Im Joo Kim, Hyun Sun, Woong |
author_facet | Shaker, Mohammed R. Lee, Ju-Hyun Park, Si-Hyung Kim, Joo Yeon Son, Gi Hoon Son, Jong Wan Park, Bae Ho Rhyu, Im Joo Kim, Hyun Sun, Woong |
author_sort | Shaker, Mohammed R. |
collection | PubMed |
description | Mammalian embryos exhibit a transition from head morphogenesis to trunk elongation to meet the demand of axial elongation. The caudal neural tube (NT) is formed with neural progenitors (NPCs) derived from neuromesodermal progenitors localized at the tail tip. However, the molecular and cellular basis of elongating NT morphogenesis is yet elusive. Here, we provide evidence that caudal NPCs exhibit strong adhesion affinity that is gradually decreased along the anteroposterior (AP) axis in mouse embryonic spinal cord and human cellular models. Strong cell-cell adhesion causes collective migration, allowing AP alignment of NPCs depending on their birthdate. We further validated that this axial adhesion gradient is associated with the extracellular matrix and is under the control of graded Wnt signaling emanating from tail buds and antagonistic retinoic acid (RA) signaling. These results suggest that progressive reduction of NPC adhesion along the AP axis is under the control of Wnt-RA molecular networks, which is essential for a proper elongation of the spinal cord. |
format | Online Article Text |
id | pubmed-7562945 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-75629452020-10-20 Anteroposterior Wnt-RA Gradient Defines Adhesion and Migration Properties of Neural Progenitors in Developing Spinal Cord Shaker, Mohammed R. Lee, Ju-Hyun Park, Si-Hyung Kim, Joo Yeon Son, Gi Hoon Son, Jong Wan Park, Bae Ho Rhyu, Im Joo Kim, Hyun Sun, Woong Stem Cell Reports Article Mammalian embryos exhibit a transition from head morphogenesis to trunk elongation to meet the demand of axial elongation. The caudal neural tube (NT) is formed with neural progenitors (NPCs) derived from neuromesodermal progenitors localized at the tail tip. However, the molecular and cellular basis of elongating NT morphogenesis is yet elusive. Here, we provide evidence that caudal NPCs exhibit strong adhesion affinity that is gradually decreased along the anteroposterior (AP) axis in mouse embryonic spinal cord and human cellular models. Strong cell-cell adhesion causes collective migration, allowing AP alignment of NPCs depending on their birthdate. We further validated that this axial adhesion gradient is associated with the extracellular matrix and is under the control of graded Wnt signaling emanating from tail buds and antagonistic retinoic acid (RA) signaling. These results suggest that progressive reduction of NPC adhesion along the AP axis is under the control of Wnt-RA molecular networks, which is essential for a proper elongation of the spinal cord. Elsevier 2020-09-24 /pmc/articles/PMC7562945/ /pubmed/32976767 http://dx.doi.org/10.1016/j.stemcr.2020.08.016 Text en © 2020 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Shaker, Mohammed R. Lee, Ju-Hyun Park, Si-Hyung Kim, Joo Yeon Son, Gi Hoon Son, Jong Wan Park, Bae Ho Rhyu, Im Joo Kim, Hyun Sun, Woong Anteroposterior Wnt-RA Gradient Defines Adhesion and Migration Properties of Neural Progenitors in Developing Spinal Cord |
title | Anteroposterior Wnt-RA Gradient Defines Adhesion and Migration Properties of Neural Progenitors in Developing Spinal Cord |
title_full | Anteroposterior Wnt-RA Gradient Defines Adhesion and Migration Properties of Neural Progenitors in Developing Spinal Cord |
title_fullStr | Anteroposterior Wnt-RA Gradient Defines Adhesion and Migration Properties of Neural Progenitors in Developing Spinal Cord |
title_full_unstemmed | Anteroposterior Wnt-RA Gradient Defines Adhesion and Migration Properties of Neural Progenitors in Developing Spinal Cord |
title_short | Anteroposterior Wnt-RA Gradient Defines Adhesion and Migration Properties of Neural Progenitors in Developing Spinal Cord |
title_sort | anteroposterior wnt-ra gradient defines adhesion and migration properties of neural progenitors in developing spinal cord |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7562945/ https://www.ncbi.nlm.nih.gov/pubmed/32976767 http://dx.doi.org/10.1016/j.stemcr.2020.08.016 |
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