Stimulation of Microvascular Networks on Sulfonated Polyrotaxane Surfaces with Immobilized Vascular Endothelial Growth Factor.
Katsuya HyodoYoshinori ArisakaSatoshi YamaguchiTetsuya YodaNobuhiko YuiPublished in: Macromolecular bioscience (2019)
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.
Keyphrases
- vascular endothelial growth factor
- endothelial cells
- biofilm formation
- growth factor
- gene expression
- high glucose
- cell proliferation
- ionic liquid
- dna methylation
- magnetic nanoparticles
- quantum dots
- staphylococcus aureus
- stem cells
- escherichia coli
- single cell
- single molecule
- bone marrow
- cystic fibrosis
- pi k akt
- vascular smooth muscle cells
- visible light