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Bioengineering of the Embryonic Cardiovascular Progenitor Cell Niche Using Electrospun Nanofibrous Saffolds

机译:使用静电纺丝纳米纤维支架的胚胎心血管祖细胞生态位的生物工程。

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As previously reported1 CPCs as identified by the vascular endothelial growth factor, receptor 2 (VEGF-R2), Flk-1 have shown greater differentiation potential when exposed to various ECM proteins. Additionally, a 3D microenvironment further enhances this differentiation potential. In order to determine the mechanism by which a 3D microenvironment enhances a cellular response, we have combined both the 3D microenvironment of the electrospun nanofibrous scaffolds with various ECM proteins we have identified as influential. We have seen that the 3D microenvironment has the ability to enhance the amount of CPCs present after at least 4 days in differentiation conditions. Further study will be required to determine the appropriate in vitro microenvironment to fully recapitulate the cardiovascular stem cell niche present in the heart and understand the specific cellular mechanisms of how these ECM proteins are able to enhance CPC copulations.
机译:如先前报道的1,通过血管内皮生长因子受体2(VEGF-R2)和Flk-1鉴定,CPC在暴露于各种ECM蛋白时显示出更大的分化潜能。此外,3D微环境进一步增强了这种分化潜力。为了确定3D微环境增强细胞反应的机制,我们将电纺纳米纤维支架的3D微环境与我们确定具有影响力的各种ECM蛋白结合在一起。我们已经看到,在分化条件下至少4天后,3D微环境具有增强存在的CPC数量的能力。需要进一步的研究来确定适当的体外微环境,以完全概括心脏中存在的心血管干细胞的生态位,并了解这些ECM蛋白如何能够增强CPC交配的具体细胞机制。

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