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An injectable hydrogel enhances tissue repair after spinal cord injury by promoting extracellular matrix remodeling

The cystic cavity that develops following injuries to brain or spinal cord is a major obstacle for tissue repair in central nervous system (CNS). Here we report that injection of imidazole-poly(organophosphazenes) (I-5), a hydrogel with thermosensitive sol–gel transition behavior, almost completely...

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Autores principales: Hong, Le Thi Anh, Kim, Young-Min, Park, Hee Hwan, Hwang, Dong Hoon, Cui, Yuexian, Lee, Eun Mi, Yahn, Stephanie, Lee, Jae K., Song, Soo-Chang, Kim, Byung Gon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5599609/
https://www.ncbi.nlm.nih.gov/pubmed/28912446
http://dx.doi.org/10.1038/s41467-017-00583-8
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author Hong, Le Thi Anh
Kim, Young-Min
Park, Hee Hwan
Hwang, Dong Hoon
Cui, Yuexian
Lee, Eun Mi
Yahn, Stephanie
Lee, Jae K.
Song, Soo-Chang
Kim, Byung Gon
author_facet Hong, Le Thi Anh
Kim, Young-Min
Park, Hee Hwan
Hwang, Dong Hoon
Cui, Yuexian
Lee, Eun Mi
Yahn, Stephanie
Lee, Jae K.
Song, Soo-Chang
Kim, Byung Gon
author_sort Hong, Le Thi Anh
collection PubMed
description The cystic cavity that develops following injuries to brain or spinal cord is a major obstacle for tissue repair in central nervous system (CNS). Here we report that injection of imidazole-poly(organophosphazenes) (I-5), a hydrogel with thermosensitive sol–gel transition behavior, almost completely eliminates cystic cavities in a clinically relevant rat spinal cord injury model. Cystic cavities are bridged by fibronectin-rich extracellular matrix. The fibrotic extracellular matrix remodeling is mediated by matrix metalloproteinase-9 expressed in macrophages within the fibrotic extracellular matrix. A poly(organophosphazenes) hydrogel lacking the imidazole moiety, which physically interacts with macrophages via histamine receptors, exhibits substantially diminished bridging effects. I-5 injection improves coordinated locomotion, and this functional recovery is accompanied by preservation of myelinated white matter and motor neurons and an increase in axonal reinnervation of the lumbar motor neurons. Our study demonstrates that dynamic interactions between inflammatory cells and injectable biomaterials can induce beneficial extracellular matrix remodeling to stimulate tissue repair following CNS injuries.
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spelling pubmed-55996092017-09-18 An injectable hydrogel enhances tissue repair after spinal cord injury by promoting extracellular matrix remodeling Hong, Le Thi Anh Kim, Young-Min Park, Hee Hwan Hwang, Dong Hoon Cui, Yuexian Lee, Eun Mi Yahn, Stephanie Lee, Jae K. Song, Soo-Chang Kim, Byung Gon Nat Commun Article The cystic cavity that develops following injuries to brain or spinal cord is a major obstacle for tissue repair in central nervous system (CNS). Here we report that injection of imidazole-poly(organophosphazenes) (I-5), a hydrogel with thermosensitive sol–gel transition behavior, almost completely eliminates cystic cavities in a clinically relevant rat spinal cord injury model. Cystic cavities are bridged by fibronectin-rich extracellular matrix. The fibrotic extracellular matrix remodeling is mediated by matrix metalloproteinase-9 expressed in macrophages within the fibrotic extracellular matrix. A poly(organophosphazenes) hydrogel lacking the imidazole moiety, which physically interacts with macrophages via histamine receptors, exhibits substantially diminished bridging effects. I-5 injection improves coordinated locomotion, and this functional recovery is accompanied by preservation of myelinated white matter and motor neurons and an increase in axonal reinnervation of the lumbar motor neurons. Our study demonstrates that dynamic interactions between inflammatory cells and injectable biomaterials can induce beneficial extracellular matrix remodeling to stimulate tissue repair following CNS injuries. Nature Publishing Group UK 2017-09-14 /pmc/articles/PMC5599609/ /pubmed/28912446 http://dx.doi.org/10.1038/s41467-017-00583-8 Text en © The Author(s) 2017 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/.
spellingShingle Article
Hong, Le Thi Anh
Kim, Young-Min
Park, Hee Hwan
Hwang, Dong Hoon
Cui, Yuexian
Lee, Eun Mi
Yahn, Stephanie
Lee, Jae K.
Song, Soo-Chang
Kim, Byung Gon
An injectable hydrogel enhances tissue repair after spinal cord injury by promoting extracellular matrix remodeling
title An injectable hydrogel enhances tissue repair after spinal cord injury by promoting extracellular matrix remodeling
title_full An injectable hydrogel enhances tissue repair after spinal cord injury by promoting extracellular matrix remodeling
title_fullStr An injectable hydrogel enhances tissue repair after spinal cord injury by promoting extracellular matrix remodeling
title_full_unstemmed An injectable hydrogel enhances tissue repair after spinal cord injury by promoting extracellular matrix remodeling
title_short An injectable hydrogel enhances tissue repair after spinal cord injury by promoting extracellular matrix remodeling
title_sort injectable hydrogel enhances tissue repair after spinal cord injury by promoting extracellular matrix remodeling
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5599609/
https://www.ncbi.nlm.nih.gov/pubmed/28912446
http://dx.doi.org/10.1038/s41467-017-00583-8
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