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In Vivo Analysis of the Neurovascular Niche in the Developing Xenopus Brain
The neurovascular niche is a specialized microenvironment formed by the interactions between neural progenitor cells (NPCs) and the vasculature. While it is thought to regulate adult neurogenesis by signaling through vascular-derived soluble cues or contacted-mediated cues, less is known about the n...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Society for Neuroscience
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5548361/ https://www.ncbi.nlm.nih.gov/pubmed/28795134 http://dx.doi.org/10.1523/ENEURO.0030-17.2017 |
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author | Lau, Melissa Li, Jianli Cline, Hollis T. |
author_facet | Lau, Melissa Li, Jianli Cline, Hollis T. |
author_sort | Lau, Melissa |
collection | PubMed |
description | The neurovascular niche is a specialized microenvironment formed by the interactions between neural progenitor cells (NPCs) and the vasculature. While it is thought to regulate adult neurogenesis by signaling through vascular-derived soluble cues or contacted-mediated cues, less is known about the neurovascular niche during development. In Xenopus laevis tadpole brain, NPCs line the ventricle and extend radial processes tipped with endfeet to the vascularized pial surface. Using in vivo labeling and time-lapse imaging in tadpoles, we find that intracardial injection of fluorescent tracers rapidly labels Sox2/3-expressing NPCs and that vascular-circulating molecules are endocytosed by NPC endfeet. Confocal imaging indicates that about half of the endfeet appear to appose the vasculature, and time-lapse analysis of NPC proliferation and endfeet-vascular interactions suggest that proliferative activity does not correlate with stable vascular apposition. Together, these findings characterize the neurovascular niche in the developing brain and suggest that, while signaling to NPCs may occur through vascular-derived soluble cues, stable contact between NPC endfeet and the vasculature is not required for developmental neurogenesis. |
format | Online Article Text |
id | pubmed-5548361 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Society for Neuroscience |
record_format | MEDLINE/PubMed |
spelling | pubmed-55483612017-08-09 In Vivo Analysis of the Neurovascular Niche in the Developing Xenopus Brain Lau, Melissa Li, Jianli Cline, Hollis T. eNeuro New Research The neurovascular niche is a specialized microenvironment formed by the interactions between neural progenitor cells (NPCs) and the vasculature. While it is thought to regulate adult neurogenesis by signaling through vascular-derived soluble cues or contacted-mediated cues, less is known about the neurovascular niche during development. In Xenopus laevis tadpole brain, NPCs line the ventricle and extend radial processes tipped with endfeet to the vascularized pial surface. Using in vivo labeling and time-lapse imaging in tadpoles, we find that intracardial injection of fluorescent tracers rapidly labels Sox2/3-expressing NPCs and that vascular-circulating molecules are endocytosed by NPC endfeet. Confocal imaging indicates that about half of the endfeet appear to appose the vasculature, and time-lapse analysis of NPC proliferation and endfeet-vascular interactions suggest that proliferative activity does not correlate with stable vascular apposition. Together, these findings characterize the neurovascular niche in the developing brain and suggest that, while signaling to NPCs may occur through vascular-derived soluble cues, stable contact between NPC endfeet and the vasculature is not required for developmental neurogenesis. Society for Neuroscience 2017-07-31 /pmc/articles/PMC5548361/ /pubmed/28795134 http://dx.doi.org/10.1523/ENEURO.0030-17.2017 Text en Copyright © 2017 Lau et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (http://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 | New Research Lau, Melissa Li, Jianli Cline, Hollis T. In Vivo Analysis of the Neurovascular Niche in the Developing Xenopus Brain |
title | In Vivo Analysis of the Neurovascular Niche in the Developing Xenopus Brain |
title_full | In Vivo Analysis of the Neurovascular Niche in the Developing Xenopus Brain |
title_fullStr | In Vivo Analysis of the Neurovascular Niche in the Developing Xenopus Brain |
title_full_unstemmed | In Vivo Analysis of the Neurovascular Niche in the Developing Xenopus Brain |
title_short | In Vivo Analysis of the Neurovascular Niche in the Developing Xenopus Brain |
title_sort | in vivo analysis of the neurovascular niche in the developing xenopus brain |
topic | New Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5548361/ https://www.ncbi.nlm.nih.gov/pubmed/28795134 http://dx.doi.org/10.1523/ENEURO.0030-17.2017 |
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