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Subventricular zone cytogenesis provides trophic support for neural repair in a mouse model of stroke

Stroke enhances proliferation of neural precursor cells within the subventricular zone (SVZ) and induces ectopic migration of newborn cells towards the site of injury. Here, we characterize the identity of cells arising from the SVZ after stroke and uncover a mechanism through which they facilitate...

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Autores principales: Williamson, Michael R., Le, Stephanie P., Franzen, Ronald L., Donlan, Nicole A., Rosow, Jill L., Nicot-Cartsonis, Mathilda S., Cervantes, Alexis, Deneen, Benjamin, Dunn, Andrew K., Jones, Theresa A., Drew, Michael R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10564905/
https://www.ncbi.nlm.nih.gov/pubmed/37816732
http://dx.doi.org/10.1038/s41467-023-42138-0
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author Williamson, Michael R.
Le, Stephanie P.
Franzen, Ronald L.
Donlan, Nicole A.
Rosow, Jill L.
Nicot-Cartsonis, Mathilda S.
Cervantes, Alexis
Deneen, Benjamin
Dunn, Andrew K.
Jones, Theresa A.
Drew, Michael R.
author_facet Williamson, Michael R.
Le, Stephanie P.
Franzen, Ronald L.
Donlan, Nicole A.
Rosow, Jill L.
Nicot-Cartsonis, Mathilda S.
Cervantes, Alexis
Deneen, Benjamin
Dunn, Andrew K.
Jones, Theresa A.
Drew, Michael R.
author_sort Williamson, Michael R.
collection PubMed
description Stroke enhances proliferation of neural precursor cells within the subventricular zone (SVZ) and induces ectopic migration of newborn cells towards the site of injury. Here, we characterize the identity of cells arising from the SVZ after stroke and uncover a mechanism through which they facilitate neural repair and functional recovery. With genetic lineage tracing, we show that SVZ-derived cells that migrate towards cortical photothrombotic stroke in mice are predominantly undifferentiated precursors. We find that ablation of neural precursor cells or conditional knockout of VEGF impairs neuronal and vascular reparative responses and worsens recovery. Replacement of VEGF is sufficient to induce neural repair and recovery. We also provide evidence that CXCL12 from peri-infarct vasculature signals to CXCR4-expressing cells arising from the SVZ to direct their ectopic migration. These results support a model in which vasculature surrounding the site of injury attracts cells from the SVZ, and these cells subsequently provide trophic support that drives neural repair and recovery.
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spelling pubmed-105649052023-10-12 Subventricular zone cytogenesis provides trophic support for neural repair in a mouse model of stroke Williamson, Michael R. Le, Stephanie P. Franzen, Ronald L. Donlan, Nicole A. Rosow, Jill L. Nicot-Cartsonis, Mathilda S. Cervantes, Alexis Deneen, Benjamin Dunn, Andrew K. Jones, Theresa A. Drew, Michael R. Nat Commun Article Stroke enhances proliferation of neural precursor cells within the subventricular zone (SVZ) and induces ectopic migration of newborn cells towards the site of injury. Here, we characterize the identity of cells arising from the SVZ after stroke and uncover a mechanism through which they facilitate neural repair and functional recovery. With genetic lineage tracing, we show that SVZ-derived cells that migrate towards cortical photothrombotic stroke in mice are predominantly undifferentiated precursors. We find that ablation of neural precursor cells or conditional knockout of VEGF impairs neuronal and vascular reparative responses and worsens recovery. Replacement of VEGF is sufficient to induce neural repair and recovery. We also provide evidence that CXCL12 from peri-infarct vasculature signals to CXCR4-expressing cells arising from the SVZ to direct their ectopic migration. These results support a model in which vasculature surrounding the site of injury attracts cells from the SVZ, and these cells subsequently provide trophic support that drives neural repair and recovery. Nature Publishing Group UK 2023-10-10 /pmc/articles/PMC10564905/ /pubmed/37816732 http://dx.doi.org/10.1038/s41467-023-42138-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Williamson, Michael R.
Le, Stephanie P.
Franzen, Ronald L.
Donlan, Nicole A.
Rosow, Jill L.
Nicot-Cartsonis, Mathilda S.
Cervantes, Alexis
Deneen, Benjamin
Dunn, Andrew K.
Jones, Theresa A.
Drew, Michael R.
Subventricular zone cytogenesis provides trophic support for neural repair in a mouse model of stroke
title Subventricular zone cytogenesis provides trophic support for neural repair in a mouse model of stroke
title_full Subventricular zone cytogenesis provides trophic support for neural repair in a mouse model of stroke
title_fullStr Subventricular zone cytogenesis provides trophic support for neural repair in a mouse model of stroke
title_full_unstemmed Subventricular zone cytogenesis provides trophic support for neural repair in a mouse model of stroke
title_short Subventricular zone cytogenesis provides trophic support for neural repair in a mouse model of stroke
title_sort subventricular zone cytogenesis provides trophic support for neural repair in a mouse model of stroke
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10564905/
https://www.ncbi.nlm.nih.gov/pubmed/37816732
http://dx.doi.org/10.1038/s41467-023-42138-0
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