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Adapting tissue-engineered in vitro CNS models for high-throughput study of neurodegeneration

Neurodegenerative conditions remain difficult to treat, with the continuing failure to see therapeutic research successfully advance to clinical trials. One of the obstacles that must be overcome is to develop enhanced models of disease. Tissue engineering techniques enable us to create organised ar...

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Autores principales: O’Rourke, Caitriona, Lee-Reeves, Charlotte, Drake, Rosemary AL, Cameron, Grant WW, Loughlin, A Jane, Phillips, James B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5415290/
https://www.ncbi.nlm.nih.gov/pubmed/28507726
http://dx.doi.org/10.1177/2041731417697920
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author O’Rourke, Caitriona
Lee-Reeves, Charlotte
Drake, Rosemary AL
Cameron, Grant WW
Loughlin, A Jane
Phillips, James B
author_facet O’Rourke, Caitriona
Lee-Reeves, Charlotte
Drake, Rosemary AL
Cameron, Grant WW
Loughlin, A Jane
Phillips, James B
author_sort O’Rourke, Caitriona
collection PubMed
description Neurodegenerative conditions remain difficult to treat, with the continuing failure to see therapeutic research successfully advance to clinical trials. One of the obstacles that must be overcome is to develop enhanced models of disease. Tissue engineering techniques enable us to create organised artificial central nervous system tissue that has the potential to improve the drug development process. This study presents a replicable model of neurodegenerative pathology through the use of engineered neural tissue co-cultures that can incorporate cells from various sources and allow degeneration and protection of neurons to be observed easily and measured, following exposure to neurotoxic compounds – okadaic acid and 1-methyl-4-phenylpyridinium. Furthermore, the technology has been miniaturised through development of a mould with 6 mm length that recreates the advantageous features of engineered neural tissue co-cultures at a scale suitable for commercial research and development. Integration of human-derived induced pluripotent stem cells aids more accurate modelling of human diseases, creating new possibilities for engineered neural tissue co-cultures and their use in drug screening.
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spelling pubmed-54152902017-05-15 Adapting tissue-engineered in vitro CNS models for high-throughput study of neurodegeneration O’Rourke, Caitriona Lee-Reeves, Charlotte Drake, Rosemary AL Cameron, Grant WW Loughlin, A Jane Phillips, James B J Tissue Eng Tissue Engineering Biomimetic Micro-environments to Direct Cell Function Neurodegenerative conditions remain difficult to treat, with the continuing failure to see therapeutic research successfully advance to clinical trials. One of the obstacles that must be overcome is to develop enhanced models of disease. Tissue engineering techniques enable us to create organised artificial central nervous system tissue that has the potential to improve the drug development process. This study presents a replicable model of neurodegenerative pathology through the use of engineered neural tissue co-cultures that can incorporate cells from various sources and allow degeneration and protection of neurons to be observed easily and measured, following exposure to neurotoxic compounds – okadaic acid and 1-methyl-4-phenylpyridinium. Furthermore, the technology has been miniaturised through development of a mould with 6 mm length that recreates the advantageous features of engineered neural tissue co-cultures at a scale suitable for commercial research and development. Integration of human-derived induced pluripotent stem cells aids more accurate modelling of human diseases, creating new possibilities for engineered neural tissue co-cultures and their use in drug screening. SAGE Publications 2017-03-15 /pmc/articles/PMC5415290/ /pubmed/28507726 http://dx.doi.org/10.1177/2041731417697920 Text en © The Author(s) 2017 http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution 3.0 License (http://www.creativecommons.org/licenses/by/3.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Tissue Engineering Biomimetic Micro-environments to Direct Cell Function
O’Rourke, Caitriona
Lee-Reeves, Charlotte
Drake, Rosemary AL
Cameron, Grant WW
Loughlin, A Jane
Phillips, James B
Adapting tissue-engineered in vitro CNS models for high-throughput study of neurodegeneration
title Adapting tissue-engineered in vitro CNS models for high-throughput study of neurodegeneration
title_full Adapting tissue-engineered in vitro CNS models for high-throughput study of neurodegeneration
title_fullStr Adapting tissue-engineered in vitro CNS models for high-throughput study of neurodegeneration
title_full_unstemmed Adapting tissue-engineered in vitro CNS models for high-throughput study of neurodegeneration
title_short Adapting tissue-engineered in vitro CNS models for high-throughput study of neurodegeneration
title_sort adapting tissue-engineered in vitro cns models for high-throughput study of neurodegeneration
topic Tissue Engineering Biomimetic Micro-environments to Direct Cell Function
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5415290/
https://www.ncbi.nlm.nih.gov/pubmed/28507726
http://dx.doi.org/10.1177/2041731417697920
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