Cargando…

The Effect of Hypothermic and Cryogenic Preservation on Engineered Neural Tissue

This study explored different approaches to preserve engineered neural tissue (EngNT), a stabilized, cellular collagen hydrogel containing columns of aligned Schwann cells for nervous system repair. The ability to preserve EngNT without disrupting cellular and extracellular components and structures...

Descripción completa

Detalles Bibliográficos
Autores principales: Day, Adam G.E., Bhangra, Kulraj Singh, Murray-Dunning, Celia, Stevanato, Lara, Phillips, James B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mary Ann Liebert, Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5686450/
https://www.ncbi.nlm.nih.gov/pubmed/28877649
http://dx.doi.org/10.1089/ten.tec.2017.0244
_version_ 1783278787267395584
author Day, Adam G.E.
Bhangra, Kulraj Singh
Murray-Dunning, Celia
Stevanato, Lara
Phillips, James B.
author_facet Day, Adam G.E.
Bhangra, Kulraj Singh
Murray-Dunning, Celia
Stevanato, Lara
Phillips, James B.
author_sort Day, Adam G.E.
collection PubMed
description This study explored different approaches to preserve engineered neural tissue (EngNT), a stabilized, cellular collagen hydrogel containing columns of aligned Schwann cells for nervous system repair. The ability to preserve EngNT without disrupting cellular and extracellular components and structures is important for clinical translation and commercialization. Stabilized cellular gels and EngNT constructs were preserved under various conditions and cell survival assessed using live/dead microscopy and metabolic assay. Optimal survival was recorded in hypothermic (4°C) conditions for 2–3 days using Hibernate(®)-A media and, for longer-term cryogenic storage (liquid nitrogen), using a mixture of 60% Dulbecco's modified Eagle's medium, 30% fetal bovine serum, and 10% dimethyl sulfoxide. Functionality and structure of preserved EngNT were assessed in coculture with dorsal root ganglion neurons, which indicated that alignment of Schwann cells and the ability of EngNT to support and guide neuronal regeneration were not disrupted. The identification of conditions that preserve EngNT will inform development of storage and transport methodologies to support clinical and commercial translation of this technology and other therapies based on cellular hydrogels.
format Online
Article
Text
id pubmed-5686450
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Mary Ann Liebert, Inc.
record_format MEDLINE/PubMed
spelling pubmed-56864502017-11-20 The Effect of Hypothermic and Cryogenic Preservation on Engineered Neural Tissue Day, Adam G.E. Bhangra, Kulraj Singh Murray-Dunning, Celia Stevanato, Lara Phillips, James B. Tissue Eng Part C Methods Methods Articles This study explored different approaches to preserve engineered neural tissue (EngNT), a stabilized, cellular collagen hydrogel containing columns of aligned Schwann cells for nervous system repair. The ability to preserve EngNT without disrupting cellular and extracellular components and structures is important for clinical translation and commercialization. Stabilized cellular gels and EngNT constructs were preserved under various conditions and cell survival assessed using live/dead microscopy and metabolic assay. Optimal survival was recorded in hypothermic (4°C) conditions for 2–3 days using Hibernate(®)-A media and, for longer-term cryogenic storage (liquid nitrogen), using a mixture of 60% Dulbecco's modified Eagle's medium, 30% fetal bovine serum, and 10% dimethyl sulfoxide. Functionality and structure of preserved EngNT were assessed in coculture with dorsal root ganglion neurons, which indicated that alignment of Schwann cells and the ability of EngNT to support and guide neuronal regeneration were not disrupted. The identification of conditions that preserve EngNT will inform development of storage and transport methodologies to support clinical and commercial translation of this technology and other therapies based on cellular hydrogels. Mary Ann Liebert, Inc. 2017-10-01 2017-10-01 /pmc/articles/PMC5686450/ /pubmed/28877649 http://dx.doi.org/10.1089/ten.tec.2017.0244 Text en © Adam G.E. Day et al. 2017; Published by Mary Ann Liebert, Inc. This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Methods Articles
Day, Adam G.E.
Bhangra, Kulraj Singh
Murray-Dunning, Celia
Stevanato, Lara
Phillips, James B.
The Effect of Hypothermic and Cryogenic Preservation on Engineered Neural Tissue
title The Effect of Hypothermic and Cryogenic Preservation on Engineered Neural Tissue
title_full The Effect of Hypothermic and Cryogenic Preservation on Engineered Neural Tissue
title_fullStr The Effect of Hypothermic and Cryogenic Preservation on Engineered Neural Tissue
title_full_unstemmed The Effect of Hypothermic and Cryogenic Preservation on Engineered Neural Tissue
title_short The Effect of Hypothermic and Cryogenic Preservation on Engineered Neural Tissue
title_sort effect of hypothermic and cryogenic preservation on engineered neural tissue
topic Methods Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5686450/
https://www.ncbi.nlm.nih.gov/pubmed/28877649
http://dx.doi.org/10.1089/ten.tec.2017.0244
work_keys_str_mv AT dayadamge theeffectofhypothermicandcryogenicpreservationonengineeredneuraltissue
AT bhangrakulrajsingh theeffectofhypothermicandcryogenicpreservationonengineeredneuraltissue
AT murraydunningcelia theeffectofhypothermicandcryogenicpreservationonengineeredneuraltissue
AT stevanatolara theeffectofhypothermicandcryogenicpreservationonengineeredneuraltissue
AT phillipsjamesb theeffectofhypothermicandcryogenicpreservationonengineeredneuraltissue
AT dayadamge effectofhypothermicandcryogenicpreservationonengineeredneuraltissue
AT bhangrakulrajsingh effectofhypothermicandcryogenicpreservationonengineeredneuraltissue
AT murraydunningcelia effectofhypothermicandcryogenicpreservationonengineeredneuraltissue
AT stevanatolara effectofhypothermicandcryogenicpreservationonengineeredneuraltissue
AT phillipsjamesb effectofhypothermicandcryogenicpreservationonengineeredneuraltissue