Subventricular zone-derived neural progenitor cells migrate along a blood vessel scaffold toward the post-stroke striatum

Takuro Kojima, Yuki Hirota, Masatsugu Ema, Satoru Takahashi, Ichiro Miyoshi, Hideyuki Okano, Kazunobu Sawamoto

Research output: Contribution to journalArticle

196 Citations (Scopus)

Abstract

The subventricular zone (SVZ) of the adult brain contains neural stem cells that have the capacity to regenerate new neurons after various insults. Brain ischemia causes damage to brain tissue and induces neural regeneration together with angiogenesis. We previously reported that, after ischemic injury in mice, SVZ-derived neural progenitor cells (NPCs) migrate into the striatum, and these NPCs are frequently associated with blood vessels in the regenerating brain tissue. Here we studied the role of blood vessels during the neural regeneration in more detail. BrdU administration experiments revealed that newly generated NPCs were associated with both newly formed and pre-existing blood vessels in the ischemic striatum, suggesting that the angiogenic environment is not essential for the neuron-blood vessel interaction. To observe migrating NPCs and blood vessels simultaneously in damaged brain tissue, we performed live imaging of cultured brain slices after ischemic injury. In this system, we virally labeled SVZ-derived NPCs in Flk1-EGFP knock-in mice in which the blood vessels are labeled with EGFP. Our results provide direct evidence that SVZ-derived NPCs migrate along blood vessels from the SVZ toward the ischemic region of the striatum. The leading process of the migrating NPCs was closely associated with blood vessels, suggesting that this interaction provides directional guidance to the NPCs. These findings suggest that blood vessels play an important role as a scaffold for NPCs migration toward the damaged brain region.

Original languageEnglish
Pages (from-to)545-554
Number of pages10
JournalStem Cells
Volume28
Issue number3
DOIs
Publication statusPublished - 2010 Mar 31

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Keywords

  • Angiogenesis
  • Cell migration
  • Live imaging
  • Neural progenitor cells
  • Stroke

ASJC Scopus subject areas

  • Molecular Medicine
  • Developmental Biology
  • Cell Biology

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