Significant Type I and Type III Collagen Production from Human Periodontal Ligament Fibroblasts in 3D Peptide Scaffolds without Extra Growth Factors

We here report the development of two peptide scaffolds designed for periodontal ligament fibroblasts. The scaffolds consist of one of the pure self-assembling peptide scaffolds RADA16 through direct coupling to short biologically active motifs. The motifs are 2-unit RGD binding sequence PRG (PRGDSG...

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Bibliographic Details
Main Authors: Kumada, Yoshiyuki (Contributor), Zhang, Shuguang (Contributor)
Other Authors: Massachusetts Institute of Technology. Center for Biomedical Engineering (Contributor)
Format: Article
Language:English
Published: Public Library of Science, 2010-09-01T20:13:08Z.
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Online Access:Get fulltext
LEADER 02121 am a22002173u 4500
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100 1 0 |a Kumada, Yoshiyuki  |e author 
100 1 0 |a Massachusetts Institute of Technology. Center for Biomedical Engineering  |e contributor 
100 1 0 |a Kumada, Yoshiyuki  |e contributor 
100 1 0 |a Kumada, Yoshiyuki  |e contributor 
100 1 0 |a Zhang, Shuguang  |e contributor 
700 1 0 |a Zhang, Shuguang  |e author 
245 0 0 |a Significant Type I and Type III Collagen Production from Human Periodontal Ligament Fibroblasts in 3D Peptide Scaffolds without Extra Growth Factors 
260 |b Public Library of Science,   |c 2010-09-01T20:13:08Z. 
856 |z Get fulltext  |u http://hdl.handle.net/1721.1/58101 
520 |a We here report the development of two peptide scaffolds designed for periodontal ligament fibroblasts. The scaffolds consist of one of the pure self-assembling peptide scaffolds RADA16 through direct coupling to short biologically active motifs. The motifs are 2-unit RGD binding sequence PRG (PRGDSGYRGDS) and laminin cell adhesion motif PDS (PDSGR). RGD and laminin have been previously shown to promote specific biological activities including periodontal ligament fibroblasts adhesion, proliferation and protein production. Compared to the pure RADA16 peptide scaffold, we here show that these designer peptide scaffolds significantly promote human periodontal ligament fibroblasts to proliferate and migrate into the scaffolds (for ~300 µm/two weeks). Moreover these peptide scaffolds significantly stimulated periodontal ligament fibroblasts to produce extracellular matrix proteins without using extra additional growth factors. Immunofluorescent images clearly demonstrated that the peptide scaffolds were almost completely covered with type I and type III collagens which were main protein components of periodontal ligament. Our results suggest that these designer self-assembling peptide nanofiber scaffolds may be useful for promoting wound healing and especially periodontal ligament tissue regeneration. 
520 |a Olympus America 
546 |a en_US 
655 7 |a Article 
773 |t PLoS ONE