Abstract

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.

The functions of newborn cells arising from the subventricular zone in response to stroke have been unclear. Here, the authors show that cells migrating from the subventricular zone after stroke promote brain repair and functional recovery in mice.

Details

Title
Subventricular zone cytogenesis provides trophic support for neural repair in a mouse model of stroke
Author
Williamson, Michael R. 1   VIAFID ORCID Logo  ; Le, Stephanie P. 2 ; Franzen, Ronald L. 3   VIAFID ORCID Logo  ; Donlan, Nicole A. 2 ; Rosow, Jill L. 2 ; Nicot-Cartsonis, Mathilda S. 4 ; Cervantes, Alexis 5 ; Deneen, Benjamin 5   VIAFID ORCID Logo  ; Dunn, Andrew K. 6 ; Jones, Theresa A. 7   VIAFID ORCID Logo  ; Drew, Michael R. 8   VIAFID ORCID Logo 

 University of Texas at Austin, Institute for Neuroscience, Austin, USA (GRID:grid.89336.37) (ISNI:0000 0004 1936 9924); Baylor College of Medicine, Center for Cell and Gene Therapy, Houston, USA (GRID:grid.39382.33) (ISNI:0000 0001 2160 926X) 
 University of Texas at Austin, Department of Psychology, Austin, USA (GRID:grid.89336.37) (ISNI:0000 0004 1936 9924) 
 University of Texas at Austin, Department of Psychology, Austin, USA (GRID:grid.89336.37) (ISNI:0000 0004 1936 9924); Baylor College of Medicine, School of Medicine, Houston, USA (GRID:grid.39382.33) (ISNI:0000 0001 2160 926X) 
 University of Texas Medical Branch at Galveston, John Sealy School of Medicine, Galveston, USA (GRID:grid.176731.5) (ISNI:0000 0001 1547 9964) 
 Baylor College of Medicine, Center for Cell and Gene Therapy, Houston, USA (GRID:grid.39382.33) (ISNI:0000 0001 2160 926X); Baylor College of Medicine, Center for Cancer Neuroscience and Department of Neurosurgery, Houston, USA (GRID:grid.39382.33) (ISNI:0000 0001 2160 926X) 
 University of Texas at Austin, Institute for Neuroscience, Austin, USA (GRID:grid.89336.37) (ISNI:0000 0004 1936 9924); University of Texas at Austin, Department of Biomedical Engineering, Austin, USA (GRID:grid.89336.37) (ISNI:0000 0004 1936 9924) 
 University of Texas at Austin, Institute for Neuroscience, Austin, USA (GRID:grid.89336.37) (ISNI:0000 0004 1936 9924); University of Texas at Austin, Department of Psychology, Austin, USA (GRID:grid.89336.37) (ISNI:0000 0004 1936 9924) 
 University of Texas at Austin, Institute for Neuroscience, Austin, USA (GRID:grid.89336.37) (ISNI:0000 0004 1936 9924); University of Texas at Austin, Center for Learning and Memory and Department of Neuroscience, Austin, USA (GRID:grid.89336.37) (ISNI:0000 0004 1936 9924) 
Pages
6341
Publication year
2023
Publication date
2023
Publisher
Nature Publishing Group
e-ISSN
20411723
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2875213729
Copyright
© The Author(s) 2023. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.