Publication | Open Access
Enhancement of differentiation efficiency of hESCs into vascular lineage cells in hypoxia via a paracrine mechanism
21
Citations
38
References
2011
Year
Cellular PhysiologyOxidative StressTranscriptional RegulationAngiogenesisRedox RegulatorVascular LineageDifferentiation EfficiencyHealth SciencesParacrine MechanismMolecular SignalingHypoxia (Medicine)Vascular BiologyHypoxia-inducible Factor 1NeovascularizationOrganogenesisVascular Endothelial Growth FactorCell BiologyDevelopmental BiologyPhysiologyVascular Lineage CellsMedicineCell Development
Hypoxia is one way of inducing differentiation due to the activation of the key regulatory factor, Hypoxia-inducible factor 1 alpha (HIF-1α). However, the action of HIF-1α on the differentiation of hESCs was unclear until now. To investigate the effect of hypoxia on the differentiation of hESCs, we compared the differentiation efficacy into vascular lineage cells under normoxic and hypoxic conditions. We observed HIF-1α expression and the related expression of pro-angiogenic factors VEGF, bFGF, Ang-1 and PDGF in hEBs cultured under hypoxic conditions. Along with this, differentiation efficacy into vascular lineage cells was improved under hypoxic conditions. When HIF-1α was blocked by echinomycin, both angiogenic factors and the differentiation efficacy were down-regulated, suggesting that the enhancement of differentiation efficacy was caused by intrinsic up-regulation of HIF-1α and these pro-angiogenic factors under hypoxic condition. This response might be primarily regulated by the HIF-1α signal pathway, and hypoxia might be the key to improving the differentiation of hESCs into vascular lineage cells. Therefore, this study demonstrated that microenvironmental changes (i.e., hypoxia) can improve differentiation efficacy of hESCs into a vascular lineage without exogenous factors via cell-intrinsic up-regulation of angiogenic factors. These facts will contribute to the regulation of stem cell fate.
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