Grafting of Gelatin on Electrospun Poly(caprolactone) Nanofibers to Improve Endothelial Cell Spreading and Proliferation and to Control Cell Orientation
We modified the surface of electrospun poly(caprolactone) (PCL) nanofibers to improve their compatibility with endothelial cells (ECs) and to show the potential application of PCL nanofibers as a blood vessel tissue-engineering scaffold. Nonwoven PCL nanofibers (PCL NF) and aligned PCL nanofibers (A...
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Veröffentlicht in: | Tissue engineering 2005-07, Vol.11 (7-8), p.1149-1158 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | We modified the surface of electrospun poly(caprolactone) (PCL) nanofibers to improve their compatibility
with endothelial cells (ECs) and to show the potential application of PCL nanofibers as a
blood vessel tissue-engineering scaffold. Nonwoven PCL nanofibers (PCL NF) and aligned PCL
nanofibers (APCL NF) were fabricated by electrospinning technology. To graft gelatin on the
nanofiber surface, PCL nanofibers were first treated with air plasma to introduce -COOH groups
on the surface, followed by covalent grafting of gelatin molecules, using water-soluble carbodiimide
as the coupling agent. The chemical change in the material surface during surface modification was
confirmed by X-ray photoelectron spectroscopy and quantified by colorimetric methods. ECs were
cultured to evaluate the cytocompatibility of surface-modified PCL NF and APCL NF. Gelatin grafting
can obviously enhance EC spreading and proliferation compared with the original material.
Moreover, gelatin-grafted APCL NF readily orients ECs along the fibers whereas unmodified APCL
NF does not. Immunostaining micrographs showed that ECs cultured on gelatin-grafted PCL NF
were able to maintain the expression of three characteristic markers: platelet-endothelial cell adhesion
molecule 1 (PECAM-1), intercellular adhesion molecule 1 (ICAM-1), and vascular cell adhesion
molecule 1 (VCAM-1). The surface-modified PCL nanofibrous material is a potential candidate
material in blood vessel tissue engineering. |
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ISSN: | 1076-3279 1557-8690 |
DOI: | 10.1089/ten.2005.11.1149 |