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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.
Afiliação
  • Williamson MR; Institute for Neuroscience, University of Texas at Austin, Austin, TX, USA. mrwillia@utexas.edu.
  • Le SP; Center for Cell and Gene Therapy, Baylor College of Medicine, Houston, TX, USA. mrwillia@utexas.edu.
  • Franzen RL; Department of Psychology, University of Texas at Austin, Austin, TX, USA.
  • Donlan NA; Department of Psychology, University of Texas at Austin, Austin, TX, USA.
  • Rosow JL; School of Medicine, Baylor College of Medicine, Houston, TX, USA.
  • Nicot-Cartsonis MS; Department of Psychology, University of Texas at Austin, Austin, TX, USA.
  • Cervantes A; Department of Psychology, University of Texas at Austin, Austin, TX, USA.
  • Deneen B; John Sealy School of Medicine, University of Texas Medical Branch at Galveston, Galveston, TX, USA.
  • Dunn AK; Center for Cell and Gene Therapy, Baylor College of Medicine, Houston, TX, USA.
  • Jones TA; Center for Cancer Neuroscience and Department of Neurosurgery, Baylor College of Medicine, Houston, TX, USA.
  • Drew MR; Center for Cell and Gene Therapy, Baylor College of Medicine, Houston, TX, USA.
Nat Commun ; 14(1): 6341, 2023 10 10.
Article em En | MEDLINE | ID: mdl-37816732
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.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Acidente Vascular Cerebral / Células-Tronco Neurais Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Acidente Vascular Cerebral / Células-Tronco Neurais Idioma: En Ano de publicação: 2023 Tipo de documento: Article