Insulin-Like Growth Factors Promote Vasculogenesis in Embryonic Stem Cells

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Insulin-Like Growth Factors Promote Vasculogenesis in Embryonic Stem Cells

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Title: Insulin-Like Growth Factors Promote Vasculogenesis in Embryonic Stem Cells
Author: Piecewicz, Stephanie M.; Hua Xiang, Soh; Pandey, Ambarish; Roy, Bhaskar; Zetter, Bruce Robert; Sengupta, Shiladitya

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Citation: Piecewicz, Stephanie M., Ambarish Pandey, Bhaskar Roy, Soh Hua Xiang, Bruce R. Zetter, and Shiladitya Sengupta. 2012. Insulin-like growth factors promote vasculogenesis in embryonic stem cells. PLoS ONE 7(2): e32191.
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Abstract: The ability of embryonic stem cells to differentiate into endothelium and form functional blood vessels has been well established and can potentially be harnessed for therapeutic angiogenesis. However, after almost two decades of investigation in this field, limited knowledge exists for directing endothelial differentiation. A better understanding of the cellular mechanisms regulating vasculogenesis is required for the development of embryonic stem cell-based models and therapies. In this study, we elucidated the mechanistic role of insulin-like growth factors (IGF1 and 2) and IGF receptors (IGFR1 and 2) in endothelial differentiation using an embryonic stem cell embryoid body model. Both IGF1 or IGF2 predisposed embryonic stem to differentiate towards a mesodermal lineage, the endothelial precursor germ layer, as well as increased the generation of significantly more endothelial cells at later stages. Inhibition of IGFR1 signaling using neutralizing antibody or a pharmacological inhibitor, picropodophyllin, significantly reduced IGF-induced mesoderm and endothelial precursor cell formation. We confirmed that IGF-IGFR1 signaling stabilizes HIF1\(\alpha\) and leads to up-regulation of VEGF during vasculogenesis in embryoid bodies. Understanding the mechanisms that are critical for vasculogenesis in various models will bring us one step closer to enabling cell based therapies for neovascularization.
Published Version: doi:10.1371/journal.pone.0032191
Other Sources: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3283730/pdf/
Terms of Use: This article is made available under the terms and conditions applicable to Other Posted Material, as set forth at http://nrs.harvard.edu/urn-3:HUL.InstRepos:dash.current.terms-of-use#LAA
Citable link to this page: http://nrs.harvard.edu/urn-3:HUL.InstRepos:8623549

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