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Cortical Reshaping and Functional Recovery Induced by Silk Fibroin Hydrogels-Encapsulated Stem Cells Implanted in Stroke Animals

The restitution of damaged circuitry and functional remodeling of peri-injured areas constitute two main mechanisms for sustaining recovery of the brain after stroke. In this study, a silk fibroin-based biomaterial efficiently supports the survival of intracerebrally implanted mesenchymal stem cells...

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Autores principales: Fernández-García, Laura, Pérez-Rigueiro, José, Martinez-Murillo, Ricardo, Panetsos, Fivos, Ramos, Milagros, Guinea, Gustavo V., González-Nieto, Daniel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6135908/
https://www.ncbi.nlm.nih.gov/pubmed/30237762
http://dx.doi.org/10.3389/fncel.2018.00296
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author Fernández-García, Laura
Pérez-Rigueiro, José
Martinez-Murillo, Ricardo
Panetsos, Fivos
Ramos, Milagros
Guinea, Gustavo V.
González-Nieto, Daniel
author_facet Fernández-García, Laura
Pérez-Rigueiro, José
Martinez-Murillo, Ricardo
Panetsos, Fivos
Ramos, Milagros
Guinea, Gustavo V.
González-Nieto, Daniel
author_sort Fernández-García, Laura
collection PubMed
description The restitution of damaged circuitry and functional remodeling of peri-injured areas constitute two main mechanisms for sustaining recovery of the brain after stroke. In this study, a silk fibroin-based biomaterial efficiently supports the survival of intracerebrally implanted mesenchymal stem cells (mSCs) and increases functional outcomes over time in a model of cortical stroke that affects the forepaw sensory and motor representations. We show that the functional mechanisms underlying recovery are related to a substantial preservation of cortical tissue in the first days after mSCs-polymer implantation, followed by delayed cortical plasticity that involved a progressive functional disconnection between the forepaw sensory (FLs(1)) and caudal motor (cFLm(1)) representations and an emergent sensory activity in peri-lesional areas belonging to cFLm(1). Our results provide evidence that mSCs integrated into silk fibroin hydrogels attenuate the cerebral damage after brain infarction inducing a delayed cortical plasticity in the peri-lesional tissue, this later a functional change described during spontaneous or training rehabilitation-induced recovery. This study shows that brain remapping and sustained recovery were experimentally favored using a stem cell-biomaterial-based approach.
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spelling pubmed-61359082018-09-20 Cortical Reshaping and Functional Recovery Induced by Silk Fibroin Hydrogels-Encapsulated Stem Cells Implanted in Stroke Animals Fernández-García, Laura Pérez-Rigueiro, José Martinez-Murillo, Ricardo Panetsos, Fivos Ramos, Milagros Guinea, Gustavo V. González-Nieto, Daniel Front Cell Neurosci Neuroscience The restitution of damaged circuitry and functional remodeling of peri-injured areas constitute two main mechanisms for sustaining recovery of the brain after stroke. In this study, a silk fibroin-based biomaterial efficiently supports the survival of intracerebrally implanted mesenchymal stem cells (mSCs) and increases functional outcomes over time in a model of cortical stroke that affects the forepaw sensory and motor representations. We show that the functional mechanisms underlying recovery are related to a substantial preservation of cortical tissue in the first days after mSCs-polymer implantation, followed by delayed cortical plasticity that involved a progressive functional disconnection between the forepaw sensory (FLs(1)) and caudal motor (cFLm(1)) representations and an emergent sensory activity in peri-lesional areas belonging to cFLm(1). Our results provide evidence that mSCs integrated into silk fibroin hydrogels attenuate the cerebral damage after brain infarction inducing a delayed cortical plasticity in the peri-lesional tissue, this later a functional change described during spontaneous or training rehabilitation-induced recovery. This study shows that brain remapping and sustained recovery were experimentally favored using a stem cell-biomaterial-based approach. Frontiers Media S.A. 2018-09-06 /pmc/articles/PMC6135908/ /pubmed/30237762 http://dx.doi.org/10.3389/fncel.2018.00296 Text en Copyright © 2018 Fernández-García, Pérez-Rigueiro, Martinez-Murillo, Panetsos, Ramos, Guinea and González-Nieto. 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 Neuroscience
Fernández-García, Laura
Pérez-Rigueiro, José
Martinez-Murillo, Ricardo
Panetsos, Fivos
Ramos, Milagros
Guinea, Gustavo V.
González-Nieto, Daniel
Cortical Reshaping and Functional Recovery Induced by Silk Fibroin Hydrogels-Encapsulated Stem Cells Implanted in Stroke Animals
title Cortical Reshaping and Functional Recovery Induced by Silk Fibroin Hydrogels-Encapsulated Stem Cells Implanted in Stroke Animals
title_full Cortical Reshaping and Functional Recovery Induced by Silk Fibroin Hydrogels-Encapsulated Stem Cells Implanted in Stroke Animals
title_fullStr Cortical Reshaping and Functional Recovery Induced by Silk Fibroin Hydrogels-Encapsulated Stem Cells Implanted in Stroke Animals
title_full_unstemmed Cortical Reshaping and Functional Recovery Induced by Silk Fibroin Hydrogels-Encapsulated Stem Cells Implanted in Stroke Animals
title_short Cortical Reshaping and Functional Recovery Induced by Silk Fibroin Hydrogels-Encapsulated Stem Cells Implanted in Stroke Animals
title_sort cortical reshaping and functional recovery induced by silk fibroin hydrogels-encapsulated stem cells implanted in stroke animals
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6135908/
https://www.ncbi.nlm.nih.gov/pubmed/30237762
http://dx.doi.org/10.3389/fncel.2018.00296
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