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Extracellular matrix from human umbilical cord-derived mesenchymal stem cells as a scaffold for peripheral nerve regeneration
The extracellular matrix, which includes collagens, laminin, or fibronectin, plays an important role in peripheral nerve regeneration. Recently, a Schwann cell-derived extracellular matrix with classical biomaterial was used to mimic the neural niche. However, extensive clinical use of Schwann cells...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4994464/ https://www.ncbi.nlm.nih.gov/pubmed/27630705 http://dx.doi.org/10.4103/1673-5374.187061 |
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author | Xiao, Bo Rao, Feng Guo, Zhi-yuan Sun, Xun Wang, Yi-guo Liu, Shu-yun Wang, Ai-yuan Guo, Quan-yi Meng, Hao-ye Zhao, Qing Peng, Jiang Wang, Yu Lu, Shi-bi |
author_facet | Xiao, Bo Rao, Feng Guo, Zhi-yuan Sun, Xun Wang, Yi-guo Liu, Shu-yun Wang, Ai-yuan Guo, Quan-yi Meng, Hao-ye Zhao, Qing Peng, Jiang Wang, Yu Lu, Shi-bi |
author_sort | Xiao, Bo |
collection | PubMed |
description | The extracellular matrix, which includes collagens, laminin, or fibronectin, plays an important role in peripheral nerve regeneration. Recently, a Schwann cell-derived extracellular matrix with classical biomaterial was used to mimic the neural niche. However, extensive clinical use of Schwann cells remains limited because of the limited origin, loss of an autologous nerve, and extended in vitro culture times. In the present study, human umbilical cord-derived mesenchymal stem cells (hUCMSCs), which are easily accessible and more proliferative than Schwann cells, were used to prepare an extracellular matrix. We identified the morphology and function of hUCMSCs and investigated their effect on peripheral nerve regeneration. Compared with a non-coated dish tissue culture, the hUCMSC-derived extracellular matrix enhanced Schwann cell proliferation, upregulated gene and protein expression levels of brain-derived neurotrophic factor, glial cell-derived neurotrophic factor, and vascular endothelial growth factor in Schwann cells, and enhanced neurite outgrowth from dorsal root ganglion neurons. These findings suggest that the hUCMSC-derived extracellular matrix promotes peripheral nerve repair and can be used as a basis for the rational design of engineered neural niches. |
format | Online Article Text |
id | pubmed-4994464 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-49944642016-09-14 Extracellular matrix from human umbilical cord-derived mesenchymal stem cells as a scaffold for peripheral nerve regeneration Xiao, Bo Rao, Feng Guo, Zhi-yuan Sun, Xun Wang, Yi-guo Liu, Shu-yun Wang, Ai-yuan Guo, Quan-yi Meng, Hao-ye Zhao, Qing Peng, Jiang Wang, Yu Lu, Shi-bi Neural Regen Res Research Article The extracellular matrix, which includes collagens, laminin, or fibronectin, plays an important role in peripheral nerve regeneration. Recently, a Schwann cell-derived extracellular matrix with classical biomaterial was used to mimic the neural niche. However, extensive clinical use of Schwann cells remains limited because of the limited origin, loss of an autologous nerve, and extended in vitro culture times. In the present study, human umbilical cord-derived mesenchymal stem cells (hUCMSCs), which are easily accessible and more proliferative than Schwann cells, were used to prepare an extracellular matrix. We identified the morphology and function of hUCMSCs and investigated their effect on peripheral nerve regeneration. Compared with a non-coated dish tissue culture, the hUCMSC-derived extracellular matrix enhanced Schwann cell proliferation, upregulated gene and protein expression levels of brain-derived neurotrophic factor, glial cell-derived neurotrophic factor, and vascular endothelial growth factor in Schwann cells, and enhanced neurite outgrowth from dorsal root ganglion neurons. These findings suggest that the hUCMSC-derived extracellular matrix promotes peripheral nerve repair and can be used as a basis for the rational design of engineered neural niches. Medknow Publications & Media Pvt Ltd 2016-07 /pmc/articles/PMC4994464/ /pubmed/27630705 http://dx.doi.org/10.4103/1673-5374.187061 Text en Copyright: © Neural Regeneration Research http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Research Article Xiao, Bo Rao, Feng Guo, Zhi-yuan Sun, Xun Wang, Yi-guo Liu, Shu-yun Wang, Ai-yuan Guo, Quan-yi Meng, Hao-ye Zhao, Qing Peng, Jiang Wang, Yu Lu, Shi-bi Extracellular matrix from human umbilical cord-derived mesenchymal stem cells as a scaffold for peripheral nerve regeneration |
title | Extracellular matrix from human umbilical cord-derived mesenchymal stem cells as a scaffold for peripheral nerve regeneration |
title_full | Extracellular matrix from human umbilical cord-derived mesenchymal stem cells as a scaffold for peripheral nerve regeneration |
title_fullStr | Extracellular matrix from human umbilical cord-derived mesenchymal stem cells as a scaffold for peripheral nerve regeneration |
title_full_unstemmed | Extracellular matrix from human umbilical cord-derived mesenchymal stem cells as a scaffold for peripheral nerve regeneration |
title_short | Extracellular matrix from human umbilical cord-derived mesenchymal stem cells as a scaffold for peripheral nerve regeneration |
title_sort | extracellular matrix from human umbilical cord-derived mesenchymal stem cells as a scaffold for peripheral nerve regeneration |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4994464/ https://www.ncbi.nlm.nih.gov/pubmed/27630705 http://dx.doi.org/10.4103/1673-5374.187061 |
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