Functionalized α-Helical Peptide Hydrogels for Neural Tissue Engineering
dc.contributor.author | Mehrban, N | |
dc.contributor.author | Zhu, B | |
dc.contributor.author | Tamagnini, F | |
dc.contributor.author | Young, FI | |
dc.contributor.author | Wasmuth, A | |
dc.contributor.author | Hudson, KL | |
dc.contributor.author | Thomson, AR | |
dc.contributor.author | Birchall, MA | |
dc.contributor.author | Randall, AD | |
dc.contributor.author | Song, B | |
dc.contributor.author | Woolfson, DN | |
dc.date.accessioned | 2017-02-24T10:14:38Z | |
dc.date.issued | 2015-03-28 | |
dc.description.abstract | Trauma to the central and peripheral nervous systems often lead to serious morbidity. Current surgical methods for repairing or replacing such damage have limitations. Tissue engineering offers a potential alternative. Here we show that functionalized α-helical-peptide hydrogels can be used to induce attachment, migration, proliferation and differentiation of murine embryonic neural stem cells (NSCs). Specifically, compared with undecorated gels, those functionalized with Arg-Gly-Asp-Ser (RGDS) peptides increase the proliferative activity of NSCs; promote their directional migration; induce differentiation, with increased expression of microtubule-associated protein-2, and a low expression of glial fibrillary acidic protein; and lead to the formation of larger neurospheres. Electrophysiological measurements from NSCs grown in RGDS-decorated gels indicate developmental progress toward mature neuron-like behavior. Our data indicate that these functional peptide hydrogels may go some way toward overcoming the limitations of current approaches to nerve-tissue repair. | en_GB |
dc.description.sponsorship | This work was supported by the Biotechnology and Biological Sciences Research Council (H01716X, D.N.W. and M.A.B.); the European Research Council (StG243261, BS; and ADG340764, D.N.W.); the Royal Society (UF051616, B.S.); the Medical Research Council (G1100623, A.D.R.); and the Engineering and Physical Sciences Research Council (Bristol Chemical Synthesis Centre for Doctoral Training, EP/G036764/1, K.L.H.). D.N.W. holds a Royal Society Wolfson Research Merit Award. | en_GB |
dc.identifier.citation | Vol. 1 (6), pp. 431 - 439 | en_GB |
dc.identifier.doi | 10.1021/acsbiomaterials.5b00051 | |
dc.identifier.uri | http://hdl.handle.net/10871/26057 | |
dc.language.iso | en | en_GB |
dc.publisher | American Chemical Society | en_GB |
dc.relation.url | http://www.ncbi.nlm.nih.gov/pubmed/26240838 | en_GB |
dc.rights | © 2015 American Chemical Society. This is an open access article published under an ACS AuthorChoice License, which permits copying and redistribution of the article or any adaptations for non-commercial purposes | en_GB |
dc.subject | RGD peptide | en_GB |
dc.subject | hydrogel | en_GB |
dc.subject | nerve tissue engineering | en_GB |
dc.subject | peptide | en_GB |
dc.subject | self-assembly | en_GB |
dc.subject | stem cell | en_GB |
dc.title | Functionalized α-Helical Peptide Hydrogels for Neural Tissue Engineering | en_GB |
dc.type | Article | en_GB |
dc.date.available | 2017-02-24T10:14:38Z | |
dc.identifier.issn | 2373-9878 | |
dc.description | This is the final version. Available on open access from the American Chemical Society via the DOI in this record. | en_GB |
dc.identifier.journal | ACS Biomaterials Science and Engineering | en_GB |
dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/4.0/ |
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Except where otherwise noted, this item's licence is described as © 2015 American Chemical Society. This is an open access article published under an ACS AuthorChoice License, which permits copying and redistribution of the article or any adaptations for non-commercial purposes