DocumentCode
11071
Title
Electrospun scaffold containing TGF-β1 promotes human mesenchymal stem cell differentiation towards a nucleus pulposus-like phenotype under hypoxia
Author
Xiang Cui ; Minghan Liu ; Jiaxu Wang ; Yue Zhou ; Qiang Xiang
Author_Institution
Dept. of Orthopedics, Third Mil. Med. Univ., Chongqing, China
Volume
9
Issue
2
fYear
2015
fDate
4 2015
Firstpage
76
Lastpage
84
Abstract
The study was aimed at evaluating the effect of electrospun scaffold containing TGF-β1 on promoting human mesenchymal stem cells (MSCs) differentiation towards a nucleus pulposus-like phenotype under hypoxia. Two kinds of nanofibrous scaffolds containing TGF-β1 were fabricated using uniaxial electrospinning (Group I) and coaxial electrospinning (Group II). Human MSCs were seeded on both kinds of scaffolds and cultured in a hypoxia chamber (2% O2), and then the scaffolds were characterised. Cell proliferation and differentiation were also evaluated after 3 weeks of cell culture. Results showed that both kinds of scaffolds shared similar diameter distributions and protein release. However, Group I scaffolds were more hydrophilic than that of Group II. Both kinds of scaffolds induced the MSCs to differentiate towards the nucleus pulposus-type phenotype in vitro. In addition, the expression of nucleus pulposus-associated genes (aggrecan, type II collagen, HIF-1α and Sox-9) in Group I increased more than that of Group II. These results indicate that electrospinning nanofibrous scaffolds containing TGF-β1 supports the differentiation of MSCs towards the pulposus-like phenotype in a hypoxia chamber, which would be a more appropriate choice for nucleus pulposus regeneration.
Keywords
biomedical materials; cellular biophysics; electrospinning; genetics; hydrophilicity; molecular biophysics; nanofabrication; nanofibres; nanomedicine; proteins; tissue engineering; HIF-1α; Sox-9; TGF-β1; aggrecan; cell culture; cell proliferation; coaxial electrospinning; diameter distributions; electrospun scaffold; human mesenchymal stem cell differentiation; hydrophilicity; hypoxia chamber; nanoflbrous scaffolds; nucleus pulposus regeneration; nucleus pulposus-associated gene expression; nucleus pulposus-like phenotype; protein release; time 3 week; uniaxial electrospinning;
fLanguage
English
Journal_Title
Nanobiotechnology, IET
Publisher
iet
ISSN
1751-8741
Type
jour
DOI
10.1049/iet-nbt.2014.0006
Filename
7076711
Link To Document