Factors released from endothelial cells exposed to flow impact adhesion, proliferation, and fate choice in the adult NSC lineage

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Authors
Dumont, C.M.
Piselli, J.
Kazi, N.
Bowman, E.
Li, G.
Linhardt, Robert J.
Temple, S.
Dai, G.
Thompson, D.M.
Issue Date
2017
Type
Article
Language
ENG
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Biology , Chemistry and chemical biology , Chemical and biological engineering , Biomedical engineering
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Abstract
The microvasculature within the neural stem cell (NSC) niche promotes self-renewal and regulates lineage progression. Previous work identified endothelial-produced soluble factors as key regulators of neural progenitor cell (NPC) fate and proliferation; however, endothelial cells (ECs) are sensitive to local hemodynamics, and the effect of this key physiological process has not been defined. In this study, we evaluated adult mouse NPC response to soluble factors isolated from static or dynamic (flow) EC cultures. Endothelial factors generated under dynamic conditions significantly increased neuronal differentiation, while those released under static conditions stimulated oligodendrocyte differentiation. Flow increases EC release of neurogenic factors and of heparin sulfate glycosaminoglycans that increase their bioactivity, likely underlying the enhanced neuronal differentiation. Additionally, endothelial factors, especially from static conditions, promoted adherent growth. Together, our data suggest that blood flow may impact proliferation, adhesion, and the neuron-glial fate choice of adult NPCs, with implications for diseases and aging that reduce flow.
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Stem Cells and Development, 26, 1199-1213
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Full Citation
Factors released from endothelial cells exposed to flow impact adhesion, proliferation, and fate choice in the adult NSC lineage, C. M. Dumont, J. Piselli, N. Kazi, E. Bowman, G. Li, R. J. Linhardt, S. Temple, G. Dai, D. M. Thompson, Stem Cells and Development, 26, 1199-1213, 2017.
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