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Harnessing neurovascular interaction to guide axon growth
Regulating the intrinsic interactions between blood vessels and nerve cells has the potential to enhance repair and regeneration of the central nervous system. Here, we evaluate the efficacy of aligned microvessels to induce and control directional axon growth from neural progenitor cells in vitro a...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6379421/ https://www.ncbi.nlm.nih.gov/pubmed/30778117 http://dx.doi.org/10.1038/s41598-019-38558-y |
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author | Partyka, Paul P. Jin, Ying Bouyer, Julien DaSilva, Angelica Godsey, George A. Nagele, Robert G. Fischer, Itzhak Galie, Peter A. |
author_facet | Partyka, Paul P. Jin, Ying Bouyer, Julien DaSilva, Angelica Godsey, George A. Nagele, Robert G. Fischer, Itzhak Galie, Peter A. |
author_sort | Partyka, Paul P. |
collection | PubMed |
description | Regulating the intrinsic interactions between blood vessels and nerve cells has the potential to enhance repair and regeneration of the central nervous system. Here, we evaluate the efficacy of aligned microvessels to induce and control directional axon growth from neural progenitor cells in vitro and host axons in a rat spinal cord injury model. Interstitial fluid flow aligned microvessels generated from co-cultures of cerebral-derived endothelial cells and pericytes in a three-dimensional scaffold. The endothelial barrier function was evaluated by immunostaining for tight junction proteins and quantifying the permeability coefficient (~10(−7) cm/s). Addition of neural progenitor cells to the co-culture resulted in the extension of Tuj-positive axons in the direction of the microvessels. To validate these findings in vivo, scaffolds were transplanted into an acute spinal cord hemisection injury with microvessels aligned with the rostral-caudal direction. At three weeks post-surgery, sagittal sections indicated close alignment between the host axons and the transplanted microvessels. Overall, this work demonstrates the efficacy of exploiting neurovascular interaction to direct axon growth in the injured spinal cord and the potential to use this strategy to facilitate central nervous system regeneration. |
format | Online Article Text |
id | pubmed-6379421 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-63794212019-02-21 Harnessing neurovascular interaction to guide axon growth Partyka, Paul P. Jin, Ying Bouyer, Julien DaSilva, Angelica Godsey, George A. Nagele, Robert G. Fischer, Itzhak Galie, Peter A. Sci Rep Article Regulating the intrinsic interactions between blood vessels and nerve cells has the potential to enhance repair and regeneration of the central nervous system. Here, we evaluate the efficacy of aligned microvessels to induce and control directional axon growth from neural progenitor cells in vitro and host axons in a rat spinal cord injury model. Interstitial fluid flow aligned microvessels generated from co-cultures of cerebral-derived endothelial cells and pericytes in a three-dimensional scaffold. The endothelial barrier function was evaluated by immunostaining for tight junction proteins and quantifying the permeability coefficient (~10(−7) cm/s). Addition of neural progenitor cells to the co-culture resulted in the extension of Tuj-positive axons in the direction of the microvessels. To validate these findings in vivo, scaffolds were transplanted into an acute spinal cord hemisection injury with microvessels aligned with the rostral-caudal direction. At three weeks post-surgery, sagittal sections indicated close alignment between the host axons and the transplanted microvessels. Overall, this work demonstrates the efficacy of exploiting neurovascular interaction to direct axon growth in the injured spinal cord and the potential to use this strategy to facilitate central nervous system regeneration. Nature Publishing Group UK 2019-02-18 /pmc/articles/PMC6379421/ /pubmed/30778117 http://dx.doi.org/10.1038/s41598-019-38558-y Text en © The Author(s) 2019 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 Partyka, Paul P. Jin, Ying Bouyer, Julien DaSilva, Angelica Godsey, George A. Nagele, Robert G. Fischer, Itzhak Galie, Peter A. Harnessing neurovascular interaction to guide axon growth |
title | Harnessing neurovascular interaction to guide axon growth |
title_full | Harnessing neurovascular interaction to guide axon growth |
title_fullStr | Harnessing neurovascular interaction to guide axon growth |
title_full_unstemmed | Harnessing neurovascular interaction to guide axon growth |
title_short | Harnessing neurovascular interaction to guide axon growth |
title_sort | harnessing neurovascular interaction to guide axon growth |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6379421/ https://www.ncbi.nlm.nih.gov/pubmed/30778117 http://dx.doi.org/10.1038/s41598-019-38558-y |
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