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Biocompatibility and Characterization of a Peptide Amphiphile Hydrogel for Applications in Peripheral Nerve Regeneration

Peripheral nerve injury is a debilitating condition for which new bioengineering solutions are needed. Autografting, the gold standard in treatment, involves sacrifice of a healthy nerve and results in loss of sensation or function at the donor site. One alternative solution to autografting is to us...

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Autores principales: Black, Katie A., Lin, Brian F., Wonder, Emily A., Desai, Seema S., Chung, Eun Ji, Ulery, Bret D., Katari, Ravi S., Tirrell, Matthew V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mary Ann Liebert, Inc. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4394881/
https://www.ncbi.nlm.nih.gov/pubmed/25626921
http://dx.doi.org/10.1089/ten.tea.2014.0297
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author Black, Katie A.
Lin, Brian F.
Wonder, Emily A.
Desai, Seema S.
Chung, Eun Ji
Ulery, Bret D.
Katari, Ravi S.
Tirrell, Matthew V.
author_facet Black, Katie A.
Lin, Brian F.
Wonder, Emily A.
Desai, Seema S.
Chung, Eun Ji
Ulery, Bret D.
Katari, Ravi S.
Tirrell, Matthew V.
author_sort Black, Katie A.
collection PubMed
description Peripheral nerve injury is a debilitating condition for which new bioengineering solutions are needed. Autografting, the gold standard in treatment, involves sacrifice of a healthy nerve and results in loss of sensation or function at the donor site. One alternative solution to autografting is to use a nerve guide conduit designed to physically guide the nerve as it regenerates across the injury gap. Such conduits are effective for short gap injuries, but fail to surpass autografting in long gap injuries. One strategy to enhance regeneration inside conduits in long gap injuries is to fill the guide conduits with a hydrogel to mimic the native extracellular matrix found in peripheral nerves. In this work, a peptide amphiphile (PA)-based hydrogel was optimized for peripheral nerve repair. Hydrogels consisting of the PA C(16)GSH were compared with a commercially available collagen gel. Schwann cells, a cell type important in the peripheral nerve regenerative cascade, were able to spread, proliferate, and migrate better on C(16)GSH gels in vitro when compared with cells seeded on collagen gels. Moreover, C(16)GSH gels were implanted subcutaneously in a murine model and were found to be biocompatible, degrade over time, and support angiogenesis without causing inflammation or a foreign body immune response. Taken together, these results help optimize and instruct the development of a new synthetic hydrogel as a luminal filler for conduit-mediated peripheral nerve repair.
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spelling pubmed-43948812015-05-13 Biocompatibility and Characterization of a Peptide Amphiphile Hydrogel for Applications in Peripheral Nerve Regeneration Black, Katie A. Lin, Brian F. Wonder, Emily A. Desai, Seema S. Chung, Eun Ji Ulery, Bret D. Katari, Ravi S. Tirrell, Matthew V. Tissue Eng Part A Original Articles Peripheral nerve injury is a debilitating condition for which new bioengineering solutions are needed. Autografting, the gold standard in treatment, involves sacrifice of a healthy nerve and results in loss of sensation or function at the donor site. One alternative solution to autografting is to use a nerve guide conduit designed to physically guide the nerve as it regenerates across the injury gap. Such conduits are effective for short gap injuries, but fail to surpass autografting in long gap injuries. One strategy to enhance regeneration inside conduits in long gap injuries is to fill the guide conduits with a hydrogel to mimic the native extracellular matrix found in peripheral nerves. In this work, a peptide amphiphile (PA)-based hydrogel was optimized for peripheral nerve repair. Hydrogels consisting of the PA C(16)GSH were compared with a commercially available collagen gel. Schwann cells, a cell type important in the peripheral nerve regenerative cascade, were able to spread, proliferate, and migrate better on C(16)GSH gels in vitro when compared with cells seeded on collagen gels. Moreover, C(16)GSH gels were implanted subcutaneously in a murine model and were found to be biocompatible, degrade over time, and support angiogenesis without causing inflammation or a foreign body immune response. Taken together, these results help optimize and instruct the development of a new synthetic hydrogel as a luminal filler for conduit-mediated peripheral nerve repair. Mary Ann Liebert, Inc. 2015-04-01 2015-03-09 /pmc/articles/PMC4394881/ /pubmed/25626921 http://dx.doi.org/10.1089/ten.tea.2014.0297 Text en © K.A. Black et al. 2015; Published by Mary Ann Liebert, Inc. This Open Access article is distributed under the terms of the Creative Commons Attribution Noncommercial Licence (http://creativecommons.org/licenses/by-nc/4.0/) which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Original Articles
Black, Katie A.
Lin, Brian F.
Wonder, Emily A.
Desai, Seema S.
Chung, Eun Ji
Ulery, Bret D.
Katari, Ravi S.
Tirrell, Matthew V.
Biocompatibility and Characterization of a Peptide Amphiphile Hydrogel for Applications in Peripheral Nerve Regeneration
title Biocompatibility and Characterization of a Peptide Amphiphile Hydrogel for Applications in Peripheral Nerve Regeneration
title_full Biocompatibility and Characterization of a Peptide Amphiphile Hydrogel for Applications in Peripheral Nerve Regeneration
title_fullStr Biocompatibility and Characterization of a Peptide Amphiphile Hydrogel for Applications in Peripheral Nerve Regeneration
title_full_unstemmed Biocompatibility and Characterization of a Peptide Amphiphile Hydrogel for Applications in Peripheral Nerve Regeneration
title_short Biocompatibility and Characterization of a Peptide Amphiphile Hydrogel for Applications in Peripheral Nerve Regeneration
title_sort biocompatibility and characterization of a peptide amphiphile hydrogel for applications in peripheral nerve regeneration
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4394881/
https://www.ncbi.nlm.nih.gov/pubmed/25626921
http://dx.doi.org/10.1089/ten.tea.2014.0297
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