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Neural crest Notch/Rbpj signaling regulates olfactory gliogenesis and neuronal migration
The neural crest‐derived ensheathing glial cells of the olfactory nerve (OECs) are unique in spanning both the peripheral and central nervous systems: they ensheathe bundles of axons projecting from olfactory receptor neurons in the nasal epithelium to their targets in the olfactory bulb. OECs are c...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6099236/ https://www.ncbi.nlm.nih.gov/pubmed/30134068 http://dx.doi.org/10.1002/dvg.23215 |
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author | Miller, Sophie R. Benito, Cristina Mirsky, Rhona Jessen, Kristján R. Baker, Clare V. H. |
author_facet | Miller, Sophie R. Benito, Cristina Mirsky, Rhona Jessen, Kristján R. Baker, Clare V. H. |
author_sort | Miller, Sophie R. |
collection | PubMed |
description | The neural crest‐derived ensheathing glial cells of the olfactory nerve (OECs) are unique in spanning both the peripheral and central nervous systems: they ensheathe bundles of axons projecting from olfactory receptor neurons in the nasal epithelium to their targets in the olfactory bulb. OECs are clinically relevant as a promising autologous cell transplantation therapy for promoting central nervous system repair. They are also important for fertility, being required for the migration of embryonic gonadotropin‐releasing hormone (GnRH) neurons from the olfactory placode along terminal nerve axons to the medial forebrain, which they enter caudal to the olfactory bulbs. Like Schwann cell precursors, OEC precursors associated with the developing olfactory nerve express the glial marker myelin protein zero and the key peripheral glial transcription factor Sox10. The transition from Schwann cell precursors to immature Schwann cells is accelerated by canonical Notch signaling via the Rbpj transcription factor. Here, we aimed to test the role of Notch/Rbpj signaling in developing OECs by blocking the pathway in both chicken and mouse. Our results suggest that Notch/Rbpj signaling prevents the cranial neural crest cells that colonize the olfactory nerve from differentiating as neurons, and at later stages contributes to the guidance of GnRH neurons. |
format | Online Article Text |
id | pubmed-6099236 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-60992362018-08-23 Neural crest Notch/Rbpj signaling regulates olfactory gliogenesis and neuronal migration Miller, Sophie R. Benito, Cristina Mirsky, Rhona Jessen, Kristján R. Baker, Clare V. H. Genesis Research Articles The neural crest‐derived ensheathing glial cells of the olfactory nerve (OECs) are unique in spanning both the peripheral and central nervous systems: they ensheathe bundles of axons projecting from olfactory receptor neurons in the nasal epithelium to their targets in the olfactory bulb. OECs are clinically relevant as a promising autologous cell transplantation therapy for promoting central nervous system repair. They are also important for fertility, being required for the migration of embryonic gonadotropin‐releasing hormone (GnRH) neurons from the olfactory placode along terminal nerve axons to the medial forebrain, which they enter caudal to the olfactory bulbs. Like Schwann cell precursors, OEC precursors associated with the developing olfactory nerve express the glial marker myelin protein zero and the key peripheral glial transcription factor Sox10. The transition from Schwann cell precursors to immature Schwann cells is accelerated by canonical Notch signaling via the Rbpj transcription factor. Here, we aimed to test the role of Notch/Rbpj signaling in developing OECs by blocking the pathway in both chicken and mouse. Our results suggest that Notch/Rbpj signaling prevents the cranial neural crest cells that colonize the olfactory nerve from differentiating as neurons, and at later stages contributes to the guidance of GnRH neurons. John Wiley and Sons Inc. 2018-08-08 2018 /pmc/articles/PMC6099236/ /pubmed/30134068 http://dx.doi.org/10.1002/dvg.23215 Text en © 2018 The Authors Genesis: The Journal of Genetics and Development Published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Miller, Sophie R. Benito, Cristina Mirsky, Rhona Jessen, Kristján R. Baker, Clare V. H. Neural crest Notch/Rbpj signaling regulates olfactory gliogenesis and neuronal migration |
title | Neural crest Notch/Rbpj signaling regulates olfactory gliogenesis and neuronal migration
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title_full | Neural crest Notch/Rbpj signaling regulates olfactory gliogenesis and neuronal migration
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title_fullStr | Neural crest Notch/Rbpj signaling regulates olfactory gliogenesis and neuronal migration
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title_full_unstemmed | Neural crest Notch/Rbpj signaling regulates olfactory gliogenesis and neuronal migration
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title_short | Neural crest Notch/Rbpj signaling regulates olfactory gliogenesis and neuronal migration
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title_sort | neural crest notch/rbpj signaling regulates olfactory gliogenesis and neuronal migration |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6099236/ https://www.ncbi.nlm.nih.gov/pubmed/30134068 http://dx.doi.org/10.1002/dvg.23215 |
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