| Literature DB >> 28557666 |
Courtney M Dumont1,2, Jennifer M Piselli1,2, Nadeem Kazi1,2, Evan Bowman2, Guoyun Li2,3, Robert J Linhardt2,3, Sally Temple4, Guohao Dai1,2, Deanna M Thompson1,2.
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.Entities:
Keywords: neural stem cells; neurogenesis; oligodendrocytes; shear stress; vascular niche
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Year: 2017 PMID: 28557666 PMCID: PMC5564022 DOI: 10.1089/scd.2016.0350
Source DB: PubMed Journal: Stem Cells Dev ISSN: 1547-3287 Impact factor: 3.272