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人脂肪来源干细胞内皮分化的环境

Milieu for Endothelial Differentiation of Human Adipose-Derived Stem Cells.

作者信息

Clark Kendra, Janorkar Amol V

机构信息

Department of Biomedical Materials Science, School of Dentistry, University of Mississippi Medical Center, Jackson, MS 39216, USA.

出版信息

Bioengineering (Basel). 2018 Oct 3;5(4):82. doi: 10.3390/bioengineering5040082.

Abstract

Human adipose-derived stem cells (hASCs) have been shown to differentiate down many lineages including endothelial lineage. We hypothesized that hASCs would more efficiently differentiate toward the endothelial lineage when formed as three-dimensional (3D) spheroids and with the addition of vascular endothelial growth factor (VEGF). Three conditions were tested: uncoated tissue culture polystyrene (TCPS) surfaces that induced a 2D monolayer formation; elastin-like polypeptide (ELP)-collagen composite hydrogel scaffolds that induced encapsulated 3D spheroid culture; and ELP-polyethyleneimine-coated TCPS surfaces that induced 3D spheroid formation in scaffold-free condition. Cells were exposed to endothelial differentiation medium containing no additional VEGF or 20 and 50 ng/mL of VEGF for 7 days and assayed for viability and endothelial differentiation markers. While endothelial differentiation media supported endothelial differentiation of hASCs, our 3D spheroid cultures augmented this differentiation and produced more von Willebrand factor than 2D cultures. Likewise, 3D cultures were able to uptake LDL, whereas the 2D cultures were not. Higher concentrations of VEGF further enhanced differentiation. Establishing angiogenesis is a key factor in regenerative medicine. Future studies aim to elucidate how to produce physiological changes such as neoangiogenesis and sprouting of vessels which may enhance the survival of regenerated tissues.

摘要

人脂肪来源干细胞(hASCs)已被证明可向包括内皮细胞系在内的多种细胞系分化。我们推测,当形成三维(3D)球体并添加血管内皮生长因子(VEGF)时,hASCs向内皮细胞系的分化效率会更高。测试了三种条件:诱导二维单层形成的未包被组织培养聚苯乙烯(TCPS)表面;诱导包封3D球体培养的弹性蛋白样多肽(ELP)-胶原复合水凝胶支架;以及在无支架条件下诱导3D球体形成的ELP-聚乙烯亚胺包被的TCPS表面。将细胞暴露于不含额外VEGF或含有20和50 ng/mL VEGF的内皮分化培养基中7天,并检测细胞活力和内皮分化标志物。虽然内皮分化培养基支持hASCs的内皮分化,但我们的3D球体培养增强了这种分化,并且比二维培养产生了更多的血管性血友病因子。同样,3D培养能够摄取低密度脂蛋白,而二维培养则不能。更高浓度的VEGF进一步增强了分化。建立血管生成是再生医学中的一个关键因素。未来的研究旨在阐明如何产生诸如新生血管生成和血管芽生等生理变化,这可能会提高再生组织的存活率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6996/6316606/403067037a94/bioengineering-05-00082-g001.jpg

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