Poly (ε-caprolactone) scaffolds functionalized by grafting NGF and GRGD promote growth and differentiation of PC12 cells

Poly(ε‐caprolactone) (PCL) scaffolds functionalized by grafting nerve growth factor (NGF) and Asp‐Arg‐Gly‐Asp (GRGD)(PCL‐NGF/GRGD) for neural tissue engineering. The influences of PCL‐NGF/GRGD scaffolds on the growth and differentiation of PC12 cells were investigated. The successfully grafting NGF...

Full description

Saved in:
Bibliographic Details
Published inJournal of biomedical materials research. Part A Vol. 102; no. 2; pp. 315 - 323
Main Authors Chung, Tze-Wen, Lai, Dar-Ming, Chen, Shin-Der, Lin, Ya-I
Format Journal Article
LanguageEnglish
Published Hoboken, NJ Blackwell Publishing Ltd 01.02.2014
Wiley-Blackwell
Wiley Subscription Services, Inc
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Poly(ε‐caprolactone) (PCL) scaffolds functionalized by grafting nerve growth factor (NGF) and Asp‐Arg‐Gly‐Asp (GRGD)(PCL‐NGF/GRGD) for neural tissue engineering. The influences of PCL‐NGF/GRGD scaffolds on the growth and differentiation of PC12 cells were investigated. The successfully grafting NGF and GRGD into PCL‐CS scaffold were verified by FTIR spectra. The densities of GRGD and NGF in the scaffolds were about 2.10×10−1 μmol/cm2 and 1.51×10−3 nmol/cm2. Growths of PC12 cells in PCL‐GRGD and PCL/NGF‐GRGD scaffolds via MTS measurements were significantly higher (p < 0.01, n = 4) than that in PCL‐CS or PCL‐NGF ones for three days of cultivation that was consistent with SEM observations. Moreover, the differentiation of PC12 cells, induced by NGF at 50 ng/mL for four days, in PCL‐NGF/GRGD scaffolds were qualitatively more numbers and longer outgrowth of neurites than those in PCL‐CS, PCL‐GRGD, and PCL‐NGF ones by SEM observations. The synergistic effects of grafting both NGF and GRGD ligands to PCL‐CS scaffolds on the growth and differentiation of PC12 cells provide a new biomaterial for neural tissue engineering. © 2013 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 102A: 315–323, 2014.
Bibliography:istex:D4CFBFFE553ECED1C74ED28255873FDD477CF008
ark:/67375/WNG-1CQBQQ5R-4
ArticleID:JBMA34693
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
ISSN:1549-3296
1552-4965
1552-4965
DOI:10.1002/jbm.a.34693