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Development of affinity-based delivery of NGF from a chondroitin sulfate biomaterial

Chondroitin sulfate is a major component of the extracellular matrix in both the central and peripheral nervous systems. Chondroitin sulfate is upregulated at injury, thus methods to promote neurite extension through chondroitin sulfate-rich matrices and synthetic scaffolds are needed. We describe t...

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Detalles Bibliográficos
Autores principales: Butterfield, Karen Chao, Conovaloff, Aaron W., Panitch, Alyssa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3549888/
https://www.ncbi.nlm.nih.gov/pubmed/23507746
http://dx.doi.org/10.4161/biom.18791
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author Butterfield, Karen Chao
Conovaloff, Aaron W.
Panitch, Alyssa
author_facet Butterfield, Karen Chao
Conovaloff, Aaron W.
Panitch, Alyssa
author_sort Butterfield, Karen Chao
collection PubMed
description Chondroitin sulfate is a major component of the extracellular matrix in both the central and peripheral nervous systems. Chondroitin sulfate is upregulated at injury, thus methods to promote neurite extension through chondroitin sulfate-rich matrices and synthetic scaffolds are needed. We describe the use of both chondroitin sulfate and a novel chondroitin sulfate-binding peptide to control the release of nerve growth factor. Interestingly, the novel chondroitin sulfate-binding peptide enhances the controlled release properties of the chondroitin sulfate gels. While introduction of chondroitin sulfate into a scaffold inhibits primary cortical outgrowth, the combination of chondroitin sulfate, chondroitin sulfate-binding peptide and nerve growth factor promotes primary cortical neurite outgrowth in chondroitin sulfate gels.
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spelling pubmed-35498882013-05-22 Development of affinity-based delivery of NGF from a chondroitin sulfate biomaterial Butterfield, Karen Chao Conovaloff, Aaron W. Panitch, Alyssa Biomatter Report Chondroitin sulfate is a major component of the extracellular matrix in both the central and peripheral nervous systems. Chondroitin sulfate is upregulated at injury, thus methods to promote neurite extension through chondroitin sulfate-rich matrices and synthetic scaffolds are needed. We describe the use of both chondroitin sulfate and a novel chondroitin sulfate-binding peptide to control the release of nerve growth factor. Interestingly, the novel chondroitin sulfate-binding peptide enhances the controlled release properties of the chondroitin sulfate gels. While introduction of chondroitin sulfate into a scaffold inhibits primary cortical outgrowth, the combination of chondroitin sulfate, chondroitin sulfate-binding peptide and nerve growth factor promotes primary cortical neurite outgrowth in chondroitin sulfate gels. Landes Bioscience 2011-10-01 /pmc/articles/PMC3549888/ /pubmed/23507746 http://dx.doi.org/10.4161/biom.18791 Text en Copyright © Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Report
Butterfield, Karen Chao
Conovaloff, Aaron W.
Panitch, Alyssa
Development of affinity-based delivery of NGF from a chondroitin sulfate biomaterial
title Development of affinity-based delivery of NGF from a chondroitin sulfate biomaterial
title_full Development of affinity-based delivery of NGF from a chondroitin sulfate biomaterial
title_fullStr Development of affinity-based delivery of NGF from a chondroitin sulfate biomaterial
title_full_unstemmed Development of affinity-based delivery of NGF from a chondroitin sulfate biomaterial
title_short Development of affinity-based delivery of NGF from a chondroitin sulfate biomaterial
title_sort development of affinity-based delivery of ngf from a chondroitin sulfate biomaterial
topic Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3549888/
https://www.ncbi.nlm.nih.gov/pubmed/23507746
http://dx.doi.org/10.4161/biom.18791
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