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Tissue Engineered Bands of Büngner for Accelerated Motor and Sensory Axonal Outgrowth

Following peripheral nerve injury comprising a segmental defect, the extent of axon regeneration decreases precipitously with increasing gap length. Schwann cells play a key role in driving axon re-growth by forming aligned tubular guidance structures called bands of Büngner, which readily occurs in...

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Autores principales: Panzer, Kate V., Burrell, Justin C., Helm, Kaila V. T., Purvis, Erin M., Zhang, Qunzhou, Le, Anh D., O’Donnell, John C., Cullen, D. Kacy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7714719/
https://www.ncbi.nlm.nih.gov/pubmed/33330416
http://dx.doi.org/10.3389/fbioe.2020.580654
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author Panzer, Kate V.
Burrell, Justin C.
Helm, Kaila V. T.
Purvis, Erin M.
Zhang, Qunzhou
Le, Anh D.
O’Donnell, John C.
Cullen, D. Kacy
author_facet Panzer, Kate V.
Burrell, Justin C.
Helm, Kaila V. T.
Purvis, Erin M.
Zhang, Qunzhou
Le, Anh D.
O’Donnell, John C.
Cullen, D. Kacy
author_sort Panzer, Kate V.
collection PubMed
description Following peripheral nerve injury comprising a segmental defect, the extent of axon regeneration decreases precipitously with increasing gap length. Schwann cells play a key role in driving axon re-growth by forming aligned tubular guidance structures called bands of Büngner, which readily occurs in distal nerve segments as well as within autografts – currently the most reliable clinically-available bridging strategy. However, host Schwann cells generally fail to infiltrate large-gap acellular scaffolds, resulting in markedly inferior outcomes and motivating the development of next-generation bridging strategies capable of fully exploiting the inherent pro-regenerative capability of Schwann cells. We sought to create preformed, implantable Schwann cell-laden microtissue that emulates the anisotropic structure and function of naturally-occurring bands of Büngner. Accordingly, we developed a biofabrication scheme leveraging biomaterial-induced self-assembly of dissociated rat primary Schwann cells into dense, fiber-like three-dimensional bundles of Schwann cells and extracellular matrix within hydrogel micro-columns. This engineered microtissue was found to be biomimetic of morphological and phenotypic features of endogenous bands of Büngner, and also demonstrated 8 and 2× faster rates of axonal extension in vitro from primary rat spinal motor neurons and dorsal root ganglion sensory neurons, respectively, compared to 3D matrix-only controls or planar Schwann cells. To our knowledge, this is the first report of accelerated motor axon outgrowth using aligned Schwann cell constructs. For translational considerations, this microtissue was also fabricated using human gingiva-derived Schwann cells as an easily accessible autologous cell source. These results demonstrate the first tissue engineered bands of Büngner (TE-BoBs) comprised of dense three-dimensional bundles of longitudinally aligned Schwann cells that are readily scalable as implantable grafts to accelerate axon regeneration across long segmental nerve defects.
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spelling pubmed-77147192020-12-15 Tissue Engineered Bands of Büngner for Accelerated Motor and Sensory Axonal Outgrowth Panzer, Kate V. Burrell, Justin C. Helm, Kaila V. T. Purvis, Erin M. Zhang, Qunzhou Le, Anh D. O’Donnell, John C. Cullen, D. Kacy Front Bioeng Biotechnol Bioengineering and Biotechnology Following peripheral nerve injury comprising a segmental defect, the extent of axon regeneration decreases precipitously with increasing gap length. Schwann cells play a key role in driving axon re-growth by forming aligned tubular guidance structures called bands of Büngner, which readily occurs in distal nerve segments as well as within autografts – currently the most reliable clinically-available bridging strategy. However, host Schwann cells generally fail to infiltrate large-gap acellular scaffolds, resulting in markedly inferior outcomes and motivating the development of next-generation bridging strategies capable of fully exploiting the inherent pro-regenerative capability of Schwann cells. We sought to create preformed, implantable Schwann cell-laden microtissue that emulates the anisotropic structure and function of naturally-occurring bands of Büngner. Accordingly, we developed a biofabrication scheme leveraging biomaterial-induced self-assembly of dissociated rat primary Schwann cells into dense, fiber-like three-dimensional bundles of Schwann cells and extracellular matrix within hydrogel micro-columns. This engineered microtissue was found to be biomimetic of morphological and phenotypic features of endogenous bands of Büngner, and also demonstrated 8 and 2× faster rates of axonal extension in vitro from primary rat spinal motor neurons and dorsal root ganglion sensory neurons, respectively, compared to 3D matrix-only controls or planar Schwann cells. To our knowledge, this is the first report of accelerated motor axon outgrowth using aligned Schwann cell constructs. For translational considerations, this microtissue was also fabricated using human gingiva-derived Schwann cells as an easily accessible autologous cell source. These results demonstrate the first tissue engineered bands of Büngner (TE-BoBs) comprised of dense three-dimensional bundles of longitudinally aligned Schwann cells that are readily scalable as implantable grafts to accelerate axon regeneration across long segmental nerve defects. Frontiers Media S.A. 2020-11-20 /pmc/articles/PMC7714719/ /pubmed/33330416 http://dx.doi.org/10.3389/fbioe.2020.580654 Text en Copyright © 2020 Panzer, Burrell, Helm, Purvis, Zhang, Le, O’Donnell and Cullen. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Bioengineering and Biotechnology
Panzer, Kate V.
Burrell, Justin C.
Helm, Kaila V. T.
Purvis, Erin M.
Zhang, Qunzhou
Le, Anh D.
O’Donnell, John C.
Cullen, D. Kacy
Tissue Engineered Bands of Büngner for Accelerated Motor and Sensory Axonal Outgrowth
title Tissue Engineered Bands of Büngner for Accelerated Motor and Sensory Axonal Outgrowth
title_full Tissue Engineered Bands of Büngner for Accelerated Motor and Sensory Axonal Outgrowth
title_fullStr Tissue Engineered Bands of Büngner for Accelerated Motor and Sensory Axonal Outgrowth
title_full_unstemmed Tissue Engineered Bands of Büngner for Accelerated Motor and Sensory Axonal Outgrowth
title_short Tissue Engineered Bands of Büngner for Accelerated Motor and Sensory Axonal Outgrowth
title_sort tissue engineered bands of büngner for accelerated motor and sensory axonal outgrowth
topic Bioengineering and Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7714719/
https://www.ncbi.nlm.nih.gov/pubmed/33330416
http://dx.doi.org/10.3389/fbioe.2020.580654
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