Key result
Stroke-activated endothelial and neural progenitor cells reciprocally enhance neurogenesis and VEGF-mediated angiogenesis.
Angiogenesis and neurogenesis are coupled processes. Using a coculture system, we tested the hypothesis that cerebral endothelial cells activated by ischemia enhance neural progenitor cell proliferation and differentiation, while neural progenitor cells isolated from the ischemic subventricular zone promote angiogenesis. Coculture of neural progenitor cells isolated from the subventricular zone of the adult normal rat with cerebral endothelial cells isolated from the stroke boundary substantially increased neural progenitor cell proliferation and neuronal differentiation and reduced astrocytic differentiation. Conditioned medium harvested from the stroke neural progenitor cells promoted capillary tube formation of normal cerebral endothelial cells. Blockage of vascular endothelial growth factor receptor 2 suppressed the effect of the endothelial cells activated by stroke on neurogenesis as well as the effect of the supernatant obtained from stroke neural progenitor cells on angiogenesis. These data suggest that angiogenesis couples to neurogenesis after stroke and vascular endothelial growth factor likely mediates this coupling.
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Teng et al. (2007) studied Stroke. Coculture of neural progenitor cells with cerebral endothelial cells from the stroke boundary vs. Blockage of vascular endothelial growth factor receptor 2 was evaluated on Neural progenitor cell proliferation, neuronal differentiation, and capillary tube formation. Stroke-activated cerebral endothelial cells enhanced neural progenitor cell proliferation and neuronal differentiation, while stroke neural progenitor cells promoted angiogenesis via VEGF mediation.
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