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|a dc
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|a Kumada, Yoshiyuki
|e author
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|a Massachusetts Institute of Technology. Center for Biomedical Engineering
|e contributor
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|a Kumada, Yoshiyuki
|e contributor
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|a Kumada, Yoshiyuki
|e contributor
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|a Zhang, Shuguang
|e contributor
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|a Zhang, Shuguang
|e author
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|a Significant Type I and Type III Collagen Production from Human Periodontal Ligament Fibroblasts in 3D Peptide Scaffolds without Extra Growth Factors
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|b Public Library of Science,
|c 2010-09-01T20:13:08Z.
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|z Get fulltext
|u http://hdl.handle.net/1721.1/58101
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|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.
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|a Olympus America
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|a en_US
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|a Article
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|t PLoS ONE
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