Biomimicking Polysaccharide Nanofibers Promote Vascular Phenotypes: A Potential Application for Vascular Tissue Engineering
The potential of electrospun pullulan/dextran (P/D) nanofibers (average diameter = 323 nm) for vascular tissue engineering applications is explored. The mechanical properties of the nanofibers are of the same order of magnitude as that of human arteries (Young's modulus ≈0.88 MPa; tensile stren...
Saved in:
Published in: | Macromolecular bioscience Vol. 12; no. 3; pp. 395 - 401 |
---|---|
Main Authors: | , , , |
Format: | Journal Article |
Language: | English |
Published: |
Weinheim
WILEY-VCH Verlag
01-03-2012
WILEY‐VCH Verlag Wiley-VCH |
Subjects: | |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | The potential of electrospun pullulan/dextran (P/D) nanofibers (average diameter = 323 nm) for vascular tissue engineering applications is explored. The mechanical properties of the nanofibers are of the same order of magnitude as that of human arteries (Young's modulus ≈0.88 MPa; tensile strength ≈0.35 MPa). It is demonstrated that the nanofiber topography enables cell adhesion and that the endothelial phenotype is maintained on the nanofibers. Moreover, P/D nanofibers support a stable confluent monolayer of endothelial cells over 14 d. SMCs seeded on nanofibers display similar levels of alpha smooth muscle actin and a lower proliferation rate than cells on 2D cultures. The observations suggest that nanofibers promote a shift to a quiescent contractile phenotype in SMCs.
The efficacy of pullulan/dextran nanofibers for vascular tissue engineering is studied. P/D nanofiber topography enables EC and SMC attachment. The endothelial phenotype is maintained for at least 14 d. P/D nanofibers support a stable confluent layer of ECs, and the morphology in SMCs suggests that nanofibers promote a shift to a quiescent contractile phenotype. |
---|---|
Bibliography: | ArticleID:MABI201100336 istex:102A6DB5708E5D8840CA2AB245C890E6B17A6513 National Medical Research Council (NMRC) Exploratory/Development - No. (NMRC/EDG/0027/2008) ark:/67375/WNG-5SFXQK8B-S Inserm, University Paris 7, University Paris 13 (Office of International Programs) MOE Tier 1 Research - No. RG36/07; No. RG75/10 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1616-5187 1616-5195 |
DOI: | 10.1002/mabi.201100336 |