| Literature DB >> 30624848 |
Katsuya Hyodo1, Yoshinori Arisaka2, Satoshi Yamaguchi1, Tetsuya Yoda1, Nobuhiko Yui2.
Abstract
Modulation of material properties and growth factor application are critical in constructing suitable cell culture environments to induce desired cellular functions. Sulfonated polyrotaxane (PRX) surfaces with immobilized vascular endothelial growth factors (VEGFs) are prepared to improve network formation in vascular endothelial cells. Sulfonated PRXs, whereby sulfonated α-cyclodextrins (α-CDs) are threaded onto a linear poly(ethylene glycol) chain capped with bulky groups at both terminals, are coated onto surfaces. The molecular mobility of sulfonated PRX surfaces is modulated by tuning the number of threading α-CDs. VEGF is immobilized onto surfaces with varying mobility. Low mobility and VEGF-immobilization reinforce cell proliferation, yes-associated protein activity, and rhoA, pdgf, ang-1, and pecam-1 gene expression. Highly mobile surfaces and soluble VEGF weakly affect these cell responses. Network formation is strongly stimulated in vascular endothelial cells only on low-mobility VEGF-immobilized surfaces, suggesting that molecular mobility and VEGF immobilization synergistically control cell function.Entities:
Keywords: human umbilical vein endothelial cell; molecular mobility; polyrotaxane; surface-immobilization of growth factor; vascular endothelial growth factor; vascular network
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Year: 2019 PMID: 30624848 DOI: 10.1002/mabi.201800346
Source DB: PubMed Journal: Macromol Biosci ISSN: 1616-5187 Impact factor: 4.979