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Functionalized α-Helical Peptide Hydrogels for Neural Tissue Engineering

[Image: see text] 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 ca...

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Autores principales: Mehrban, Nazia, Zhu, Bangfu, Tamagnini, Francesco, Young, Fraser I., Wasmuth, Alexandra, Hudson, Kieran L., Thomson, Andrew R., Birchall, Martin A., Randall, Andrew D., Song, Bing, Woolfson, Derek N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2015
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4517957/
https://www.ncbi.nlm.nih.gov/pubmed/26240838
http://dx.doi.org/10.1021/acsbiomaterials.5b00051
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author Mehrban, Nazia
Zhu, Bangfu
Tamagnini, Francesco
Young, Fraser I.
Wasmuth, Alexandra
Hudson, Kieran L.
Thomson, Andrew R.
Birchall, Martin A.
Randall, Andrew D.
Song, Bing
Woolfson, Derek N.
author_facet Mehrban, Nazia
Zhu, Bangfu
Tamagnini, Francesco
Young, Fraser I.
Wasmuth, Alexandra
Hudson, Kieran L.
Thomson, Andrew R.
Birchall, Martin A.
Randall, Andrew D.
Song, Bing
Woolfson, Derek N.
author_sort Mehrban, Nazia
collection PubMed
description [Image: see text] 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.
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spelling pubmed-45179572015-08-01 Functionalized α-Helical Peptide Hydrogels for Neural Tissue Engineering Mehrban, Nazia Zhu, Bangfu Tamagnini, Francesco Young, Fraser I. Wasmuth, Alexandra Hudson, Kieran L. Thomson, Andrew R. Birchall, Martin A. Randall, Andrew D. Song, Bing Woolfson, Derek N. ACS Biomater Sci Eng [Image: see text] 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. American Chemical Society 2015-04-28 2015-06-08 /pmc/articles/PMC4517957/ /pubmed/26240838 http://dx.doi.org/10.1021/acsbiomaterials.5b00051 Text en Copyright © 2015 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Mehrban, Nazia
Zhu, Bangfu
Tamagnini, Francesco
Young, Fraser I.
Wasmuth, Alexandra
Hudson, Kieran L.
Thomson, Andrew R.
Birchall, Martin A.
Randall, Andrew D.
Song, Bing
Woolfson, Derek N.
Functionalized α-Helical Peptide Hydrogels for Neural Tissue Engineering
title Functionalized α-Helical Peptide Hydrogels for Neural Tissue Engineering
title_full Functionalized α-Helical Peptide Hydrogels for Neural Tissue Engineering
title_fullStr Functionalized α-Helical Peptide Hydrogels for Neural Tissue Engineering
title_full_unstemmed Functionalized α-Helical Peptide Hydrogels for Neural Tissue Engineering
title_short Functionalized α-Helical Peptide Hydrogels for Neural Tissue Engineering
title_sort functionalized α-helical peptide hydrogels for neural tissue engineering
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4517957/
https://www.ncbi.nlm.nih.gov/pubmed/26240838
http://dx.doi.org/10.1021/acsbiomaterials.5b00051
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