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Fabrication of homotypic neural ribbons as a multiplex platform optimized for spinal cord delivery

Cell therapy for the injured spinal cord will rely on combined advances in human stem cell technologies and delivery strategies. Here we encapsulate homotypic spinal cord neural stem cells (scNSCs) in an alginate-based neural ribbon delivery platform. We perform a comprehensive in vitro analysis and...

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Autores principales: Olmsted, Zachary T., Stigliano, Cinzia, Badri, Abinaya, Zhang, Fuming, Williams, Asher, Koffas, Mattheos A. G., Xie, Yubing, Linhardt, Robert J., Cibelli, Jose, Horner, Philip J., Paluh, Janet L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7395100/
https://www.ncbi.nlm.nih.gov/pubmed/32737387
http://dx.doi.org/10.1038/s41598-020-69274-7
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author Olmsted, Zachary T.
Stigliano, Cinzia
Badri, Abinaya
Zhang, Fuming
Williams, Asher
Koffas, Mattheos A. G.
Xie, Yubing
Linhardt, Robert J.
Cibelli, Jose
Horner, Philip J.
Paluh, Janet L.
author_facet Olmsted, Zachary T.
Stigliano, Cinzia
Badri, Abinaya
Zhang, Fuming
Williams, Asher
Koffas, Mattheos A. G.
Xie, Yubing
Linhardt, Robert J.
Cibelli, Jose
Horner, Philip J.
Paluh, Janet L.
author_sort Olmsted, Zachary T.
collection PubMed
description Cell therapy for the injured spinal cord will rely on combined advances in human stem cell technologies and delivery strategies. Here we encapsulate homotypic spinal cord neural stem cells (scNSCs) in an alginate-based neural ribbon delivery platform. We perform a comprehensive in vitro analysis and qualitatively demonstrate graft survival and injury site retention using a rat C4 hemi-contusion model. Pre-configured neural ribbons are transport-stable modules that enable site-ready injection, and can support scNSC survival and retention in vivo. Neural ribbons offer multifunctionality in vitro including co-encapsulation of the injury site extracellular matrix modifier chondroitinase ABC (chABC), tested here in glial scar models, and ability of cervically-patterned scNSCs to differentiate within neural ribbons and project axons for integration with 3-D external matrices. This is the first extensive in vitro characterization of neural ribbon technology, and constitutes a plausible method for reproducible delivery, placement, and retention of viable neural cells in vivo.
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spelling pubmed-73951002020-08-03 Fabrication of homotypic neural ribbons as a multiplex platform optimized for spinal cord delivery Olmsted, Zachary T. Stigliano, Cinzia Badri, Abinaya Zhang, Fuming Williams, Asher Koffas, Mattheos A. G. Xie, Yubing Linhardt, Robert J. Cibelli, Jose Horner, Philip J. Paluh, Janet L. Sci Rep Article Cell therapy for the injured spinal cord will rely on combined advances in human stem cell technologies and delivery strategies. Here we encapsulate homotypic spinal cord neural stem cells (scNSCs) in an alginate-based neural ribbon delivery platform. We perform a comprehensive in vitro analysis and qualitatively demonstrate graft survival and injury site retention using a rat C4 hemi-contusion model. Pre-configured neural ribbons are transport-stable modules that enable site-ready injection, and can support scNSC survival and retention in vivo. Neural ribbons offer multifunctionality in vitro including co-encapsulation of the injury site extracellular matrix modifier chondroitinase ABC (chABC), tested here in glial scar models, and ability of cervically-patterned scNSCs to differentiate within neural ribbons and project axons for integration with 3-D external matrices. This is the first extensive in vitro characterization of neural ribbon technology, and constitutes a plausible method for reproducible delivery, placement, and retention of viable neural cells in vivo. Nature Publishing Group UK 2020-07-31 /pmc/articles/PMC7395100/ /pubmed/32737387 http://dx.doi.org/10.1038/s41598-020-69274-7 Text en © This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2020 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Olmsted, Zachary T.
Stigliano, Cinzia
Badri, Abinaya
Zhang, Fuming
Williams, Asher
Koffas, Mattheos A. G.
Xie, Yubing
Linhardt, Robert J.
Cibelli, Jose
Horner, Philip J.
Paluh, Janet L.
Fabrication of homotypic neural ribbons as a multiplex platform optimized for spinal cord delivery
title Fabrication of homotypic neural ribbons as a multiplex platform optimized for spinal cord delivery
title_full Fabrication of homotypic neural ribbons as a multiplex platform optimized for spinal cord delivery
title_fullStr Fabrication of homotypic neural ribbons as a multiplex platform optimized for spinal cord delivery
title_full_unstemmed Fabrication of homotypic neural ribbons as a multiplex platform optimized for spinal cord delivery
title_short Fabrication of homotypic neural ribbons as a multiplex platform optimized for spinal cord delivery
title_sort fabrication of homotypic neural ribbons as a multiplex platform optimized for spinal cord delivery
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7395100/
https://www.ncbi.nlm.nih.gov/pubmed/32737387
http://dx.doi.org/10.1038/s41598-020-69274-7
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