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Wnt Signaling in Neural Crest Ontogenesis and Oncogenesis
Neural crest (NC) cells are a temporary population of multipotent stem cells that generate a diverse array of cell types, including craniofacial bone and cartilage, smooth muscle cells, melanocytes, and peripheral neurons and glia during embryonic development. Defective neural crest development can...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6829301/ https://www.ncbi.nlm.nih.gov/pubmed/31569501 http://dx.doi.org/10.3390/cells8101173 |
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author | Ji, Yu Hao, Hongyan Reynolds, Kurt McMahon, Moira Zhou, Chengji J. |
author_facet | Ji, Yu Hao, Hongyan Reynolds, Kurt McMahon, Moira Zhou, Chengji J. |
author_sort | Ji, Yu |
collection | PubMed |
description | Neural crest (NC) cells are a temporary population of multipotent stem cells that generate a diverse array of cell types, including craniofacial bone and cartilage, smooth muscle cells, melanocytes, and peripheral neurons and glia during embryonic development. Defective neural crest development can cause severe and common structural birth defects, such as craniofacial anomalies and congenital heart disease. In the early vertebrate embryos, NC cells emerge from the dorsal edge of the neural tube during neurulation and then migrate extensively throughout the anterior-posterior body axis to generate numerous derivatives. Wnt signaling plays essential roles in embryonic development and cancer. This review summarizes current understanding of Wnt signaling in NC cell induction, delamination, migration, multipotency, and fate determination, as well as in NC-derived cancers. |
format | Online Article Text |
id | pubmed-6829301 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-68293012019-11-18 Wnt Signaling in Neural Crest Ontogenesis and Oncogenesis Ji, Yu Hao, Hongyan Reynolds, Kurt McMahon, Moira Zhou, Chengji J. Cells Review Neural crest (NC) cells are a temporary population of multipotent stem cells that generate a diverse array of cell types, including craniofacial bone and cartilage, smooth muscle cells, melanocytes, and peripheral neurons and glia during embryonic development. Defective neural crest development can cause severe and common structural birth defects, such as craniofacial anomalies and congenital heart disease. In the early vertebrate embryos, NC cells emerge from the dorsal edge of the neural tube during neurulation and then migrate extensively throughout the anterior-posterior body axis to generate numerous derivatives. Wnt signaling plays essential roles in embryonic development and cancer. This review summarizes current understanding of Wnt signaling in NC cell induction, delamination, migration, multipotency, and fate determination, as well as in NC-derived cancers. MDPI 2019-09-29 /pmc/articles/PMC6829301/ /pubmed/31569501 http://dx.doi.org/10.3390/cells8101173 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Ji, Yu Hao, Hongyan Reynolds, Kurt McMahon, Moira Zhou, Chengji J. Wnt Signaling in Neural Crest Ontogenesis and Oncogenesis |
title | Wnt Signaling in Neural Crest Ontogenesis and Oncogenesis |
title_full | Wnt Signaling in Neural Crest Ontogenesis and Oncogenesis |
title_fullStr | Wnt Signaling in Neural Crest Ontogenesis and Oncogenesis |
title_full_unstemmed | Wnt Signaling in Neural Crest Ontogenesis and Oncogenesis |
title_short | Wnt Signaling in Neural Crest Ontogenesis and Oncogenesis |
title_sort | wnt signaling in neural crest ontogenesis and oncogenesis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6829301/ https://www.ncbi.nlm.nih.gov/pubmed/31569501 http://dx.doi.org/10.3390/cells8101173 |
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