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Regenerating the Injured Spinal Cord at the Chronic Phase by Engineered iPSCs‐Derived 3D Neuronal Networks
Cell therapy using induced pluripotent stem cell‐derived neurons is considered a promising approach to regenerate the injured spinal cord (SC). However, the scar formed at the chronic phase is not a permissive microenvironment for cell or biomaterial engraftment or for tissue assembly. Engineering o...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9008789/ https://www.ncbi.nlm.nih.gov/pubmed/35128819 http://dx.doi.org/10.1002/advs.202105694 |
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author | Wertheim, Lior Edri, Reuven Goldshmit, Yona Kagan, Tomer Noor, Nadav Ruban, Angela Shapira, Assaf Gat‐Viks, Irit Assaf, Yaniv Dvir, Tal |
author_facet | Wertheim, Lior Edri, Reuven Goldshmit, Yona Kagan, Tomer Noor, Nadav Ruban, Angela Shapira, Assaf Gat‐Viks, Irit Assaf, Yaniv Dvir, Tal |
author_sort | Wertheim, Lior |
collection | PubMed |
description | Cell therapy using induced pluripotent stem cell‐derived neurons is considered a promising approach to regenerate the injured spinal cord (SC). However, the scar formed at the chronic phase is not a permissive microenvironment for cell or biomaterial engraftment or for tissue assembly. Engineering of a functional human neuronal network is now reported by mimicking the embryonic development of the SC in a 3D dynamic biomaterial‐based microenvironment. Throughout the in vitro cultivation stage, the system's components have a synergistic effect, providing appropriate cues for SC neurogenesis. While the initial biomaterial supported efficient cell differentiation in 3D, the cells remodeled it to provide an inductive microenvironment for the assembly of functional SC implants. The engineered tissues are characterized for morphology and function, and their therapeutic potential is investigated, revealing improved structural and functional outcomes after acute and chronic SC injuries. Such technology is envisioned to be translated to the clinic to rewire human injured SC. |
format | Online Article Text |
id | pubmed-9008789 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-90087892022-04-15 Regenerating the Injured Spinal Cord at the Chronic Phase by Engineered iPSCs‐Derived 3D Neuronal Networks Wertheim, Lior Edri, Reuven Goldshmit, Yona Kagan, Tomer Noor, Nadav Ruban, Angela Shapira, Assaf Gat‐Viks, Irit Assaf, Yaniv Dvir, Tal Adv Sci (Weinh) Research Articles Cell therapy using induced pluripotent stem cell‐derived neurons is considered a promising approach to regenerate the injured spinal cord (SC). However, the scar formed at the chronic phase is not a permissive microenvironment for cell or biomaterial engraftment or for tissue assembly. Engineering of a functional human neuronal network is now reported by mimicking the embryonic development of the SC in a 3D dynamic biomaterial‐based microenvironment. Throughout the in vitro cultivation stage, the system's components have a synergistic effect, providing appropriate cues for SC neurogenesis. While the initial biomaterial supported efficient cell differentiation in 3D, the cells remodeled it to provide an inductive microenvironment for the assembly of functional SC implants. The engineered tissues are characterized for morphology and function, and their therapeutic potential is investigated, revealing improved structural and functional outcomes after acute and chronic SC injuries. Such technology is envisioned to be translated to the clinic to rewire human injured SC. John Wiley and Sons Inc. 2022-02-07 /pmc/articles/PMC9008789/ /pubmed/35128819 http://dx.doi.org/10.1002/advs.202105694 Text en © 2022 The Authors. Advanced Science published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Wertheim, Lior Edri, Reuven Goldshmit, Yona Kagan, Tomer Noor, Nadav Ruban, Angela Shapira, Assaf Gat‐Viks, Irit Assaf, Yaniv Dvir, Tal Regenerating the Injured Spinal Cord at the Chronic Phase by Engineered iPSCs‐Derived 3D Neuronal Networks |
title | Regenerating the Injured Spinal Cord at the Chronic Phase by Engineered iPSCs‐Derived 3D Neuronal Networks |
title_full | Regenerating the Injured Spinal Cord at the Chronic Phase by Engineered iPSCs‐Derived 3D Neuronal Networks |
title_fullStr | Regenerating the Injured Spinal Cord at the Chronic Phase by Engineered iPSCs‐Derived 3D Neuronal Networks |
title_full_unstemmed | Regenerating the Injured Spinal Cord at the Chronic Phase by Engineered iPSCs‐Derived 3D Neuronal Networks |
title_short | Regenerating the Injured Spinal Cord at the Chronic Phase by Engineered iPSCs‐Derived 3D Neuronal Networks |
title_sort | regenerating the injured spinal cord at the chronic phase by engineered ipscs‐derived 3d neuronal networks |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9008789/ https://www.ncbi.nlm.nih.gov/pubmed/35128819 http://dx.doi.org/10.1002/advs.202105694 |
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