Neovascularization in the adult central nervous system occurs as a response to several pathophysiological conditions such as ischemia, wound repair, or neoplasia. Endothelial cells from different blood vessel types, different organs, and different species are heterogeneous; therefore, the appropriat
In vitro culture of rat neuromicrovascular endothelial cells on polymeric scaffolds
β Scribed by Conconi, Maria Teresa ;Lora, Silvano ;Baiguera, Silvia ;Boscolo, Elisa ;Folin, Marcella ;Scienza, Renato ;Rebuffat, Piera ;Parnigotto, Pier Paolo ;Nussdorfer, Gastone Giovanni
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 372 KB
- Volume
- 71A
- Category
- Article
- ISSN
- 0021-9304
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β¦ Synopsis
Abstract
Polyphosphazenes are polymers possessing a skeleton composed of alternating phosphorous and nitrogen atoms, and two sideβmoieties linked to each phosphorous atom. Polyphosphazenes with amino acid esters as sideβmoieties are biocompatible and biodegradable polymers. Two polyphosphazenes, poly[bis(ethyl alanate) phosphazene] and poly[(ethyl phenylalanate)~0.8~(ethyl alanate)~0.8~(ethyl glycinate)~0.4~ phosphazene] (PPAGP) were synthesized, and processed to form small fibers. Their ability to support rat neuromicrovascular endothelial cell (EC) adhesion and growth has been studied, using poly(D,Lβlactic acid) as reference compound. Scanning electron microscopy revealed that both poly[bis(ethyl alanate) phosphazene] and PPAGP fibers were thinner than poly(D,Lβlactic acid) fibers, and possessed a more irregular and porous surface. All polymers increased EC adhesion, compared with polystyrene, but only polyphosphazenes were able to improve EC growth. The highest increase in EC proliferation was induced by PPAGP, which, as revealed by environmental scanning electron microscopy, was also able to induce ECs to arrange into tubular structures. The conclusion is drawn that PPAGP may provide the best scaffold for engineered blood vessels, because it promotes adhesion, growth, and organization of ECs into capillaryβlike structures. Β© 2004 Wiley Periodicals, Inc. J Biomed Mater Res 71A: 669β674, 2004
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