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Human Oligodendrogenic Neural Progenitor Cells Delivered with Chondroitinase ABC Facilitate Functional Repair of Chronic Spinal Cord Injury
Treatment of chronic spinal cord injury (SCI) is challenging due to cell loss, cyst formation, and the glial scar. Previously, we reported on the therapeutic potential of a neural progenitor cell (NPC) and chondroitinase ABC (ChABC) combinatorial therapy for chronic SCI. However, the source of NPCs...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6294173/ https://www.ncbi.nlm.nih.gov/pubmed/30472009 http://dx.doi.org/10.1016/j.stemcr.2018.10.017 |
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author | Nori, Satoshi Khazaei, Mohamad Ahuja, Christopher S. Yokota, Kazuya Ahlfors, Jan-Eric Liu, Yang Wang, Jian Shibata, Shinsuke Chio, Jonathon Hettiaratchi, Marian H. Führmann, Tobias Shoichet, Molly S. Fehlings, Michael G. |
author_facet | Nori, Satoshi Khazaei, Mohamad Ahuja, Christopher S. Yokota, Kazuya Ahlfors, Jan-Eric Liu, Yang Wang, Jian Shibata, Shinsuke Chio, Jonathon Hettiaratchi, Marian H. Führmann, Tobias Shoichet, Molly S. Fehlings, Michael G. |
author_sort | Nori, Satoshi |
collection | PubMed |
description | Treatment of chronic spinal cord injury (SCI) is challenging due to cell loss, cyst formation, and the glial scar. Previously, we reported on the therapeutic potential of a neural progenitor cell (NPC) and chondroitinase ABC (ChABC) combinatorial therapy for chronic SCI. However, the source of NPCs and delivery system required for ChABC remained barriers to clinical application. Here, we investigated directly reprogrammed human NPCs biased toward an oligodendrogenic fate (oNPCs) in combination with sustained delivery of ChABC using an innovative affinity release strategy in a crosslinked methylcellulose biomaterial for the treatment of chronic SCI in an immunodeficient rat model. This combinatorial therapy increased long-term survival of oNPCs around the lesion epicenter, facilitated greater oligodendrocyte differentiation, remyelination of the spared axons by engrafted oNPCs, enhanced synaptic connectivity with anterior horn cells and neurobehavioral recovery. This combinatorial therapy is a promising strategy to regenerate the chronically injured spinal cord. |
format | Online Article Text |
id | pubmed-6294173 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-62941732018-12-21 Human Oligodendrogenic Neural Progenitor Cells Delivered with Chondroitinase ABC Facilitate Functional Repair of Chronic Spinal Cord Injury Nori, Satoshi Khazaei, Mohamad Ahuja, Christopher S. Yokota, Kazuya Ahlfors, Jan-Eric Liu, Yang Wang, Jian Shibata, Shinsuke Chio, Jonathon Hettiaratchi, Marian H. Führmann, Tobias Shoichet, Molly S. Fehlings, Michael G. Stem Cell Reports Article Treatment of chronic spinal cord injury (SCI) is challenging due to cell loss, cyst formation, and the glial scar. Previously, we reported on the therapeutic potential of a neural progenitor cell (NPC) and chondroitinase ABC (ChABC) combinatorial therapy for chronic SCI. However, the source of NPCs and delivery system required for ChABC remained barriers to clinical application. Here, we investigated directly reprogrammed human NPCs biased toward an oligodendrogenic fate (oNPCs) in combination with sustained delivery of ChABC using an innovative affinity release strategy in a crosslinked methylcellulose biomaterial for the treatment of chronic SCI in an immunodeficient rat model. This combinatorial therapy increased long-term survival of oNPCs around the lesion epicenter, facilitated greater oligodendrocyte differentiation, remyelination of the spared axons by engrafted oNPCs, enhanced synaptic connectivity with anterior horn cells and neurobehavioral recovery. This combinatorial therapy is a promising strategy to regenerate the chronically injured spinal cord. Elsevier 2018-11-21 /pmc/articles/PMC6294173/ /pubmed/30472009 http://dx.doi.org/10.1016/j.stemcr.2018.10.017 Text en © 2018 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Nori, Satoshi Khazaei, Mohamad Ahuja, Christopher S. Yokota, Kazuya Ahlfors, Jan-Eric Liu, Yang Wang, Jian Shibata, Shinsuke Chio, Jonathon Hettiaratchi, Marian H. Führmann, Tobias Shoichet, Molly S. Fehlings, Michael G. Human Oligodendrogenic Neural Progenitor Cells Delivered with Chondroitinase ABC Facilitate Functional Repair of Chronic Spinal Cord Injury |
title | Human Oligodendrogenic Neural Progenitor Cells Delivered with Chondroitinase ABC Facilitate Functional Repair of Chronic Spinal Cord Injury |
title_full | Human Oligodendrogenic Neural Progenitor Cells Delivered with Chondroitinase ABC Facilitate Functional Repair of Chronic Spinal Cord Injury |
title_fullStr | Human Oligodendrogenic Neural Progenitor Cells Delivered with Chondroitinase ABC Facilitate Functional Repair of Chronic Spinal Cord Injury |
title_full_unstemmed | Human Oligodendrogenic Neural Progenitor Cells Delivered with Chondroitinase ABC Facilitate Functional Repair of Chronic Spinal Cord Injury |
title_short | Human Oligodendrogenic Neural Progenitor Cells Delivered with Chondroitinase ABC Facilitate Functional Repair of Chronic Spinal Cord Injury |
title_sort | human oligodendrogenic neural progenitor cells delivered with chondroitinase abc facilitate functional repair of chronic spinal cord injury |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6294173/ https://www.ncbi.nlm.nih.gov/pubmed/30472009 http://dx.doi.org/10.1016/j.stemcr.2018.10.017 |
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