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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...

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Autores principales: Partyka, Paul P., Jin, Ying, Bouyer, Julien, DaSilva, Angelica, Godsey, George A., Nagele, Robert G., Fischer, Itzhak, Galie, Peter A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
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.
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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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