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The SH-SY5Y cell line in Parkinson’s disease research: a systematic review
Parkinson’s disease (PD) is a devastating and highly prevalent neurodegenerative disease for which only symptomatic treatment is available. In order to develop a truly effective disease-modifying therapy, improvement of our current understanding of the molecular and cellular mechanisms underlying PD...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5259880/ https://www.ncbi.nlm.nih.gov/pubmed/28118852 http://dx.doi.org/10.1186/s13024-017-0149-0 |
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author | Xicoy, Helena Wieringa, Bé Martens, Gerard J.M. |
author_facet | Xicoy, Helena Wieringa, Bé Martens, Gerard J.M. |
author_sort | Xicoy, Helena |
collection | PubMed |
description | Parkinson’s disease (PD) is a devastating and highly prevalent neurodegenerative disease for which only symptomatic treatment is available. In order to develop a truly effective disease-modifying therapy, improvement of our current understanding of the molecular and cellular mechanisms underlying PD pathogenesis and progression is crucial. For this purpose, standardization of research protocols and disease models is necessary. As human dopaminergic neurons, the cells mainly affected in PD, are difficult to obtain and maintain as primary cells, current PD research is mostly performed with permanently established neuronal cell models, in particular the neuroblastoma SH-SY5Y lineage. This cell line is frequently chosen because of its human origin, catecholaminergic (though not strictly dopaminergic) neuronal properties, and ease of maintenance. However, there is no consensus on many fundamental aspects that are associated with its use, such as the effects of culture media composition and of variations in differentiation protocols. Here we present the outcome of a systematic review of scientific articles that have used SH-SY5Y cells to explore PD. We describe the cell source, culture conditions, differentiation protocols, methods/approaches used to mimic PD and the preclinical validation of the SH-SY5Y findings by employing alternative cellular and animal models. Thus, this overview may help to standardize the use of the SH-SY5Y cell line in PD research and serve as a future user’s guide. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13024-017-0149-0) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5259880 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-52598802017-01-30 The SH-SY5Y cell line in Parkinson’s disease research: a systematic review Xicoy, Helena Wieringa, Bé Martens, Gerard J.M. Mol Neurodegener Review Parkinson’s disease (PD) is a devastating and highly prevalent neurodegenerative disease for which only symptomatic treatment is available. In order to develop a truly effective disease-modifying therapy, improvement of our current understanding of the molecular and cellular mechanisms underlying PD pathogenesis and progression is crucial. For this purpose, standardization of research protocols and disease models is necessary. As human dopaminergic neurons, the cells mainly affected in PD, are difficult to obtain and maintain as primary cells, current PD research is mostly performed with permanently established neuronal cell models, in particular the neuroblastoma SH-SY5Y lineage. This cell line is frequently chosen because of its human origin, catecholaminergic (though not strictly dopaminergic) neuronal properties, and ease of maintenance. However, there is no consensus on many fundamental aspects that are associated with its use, such as the effects of culture media composition and of variations in differentiation protocols. Here we present the outcome of a systematic review of scientific articles that have used SH-SY5Y cells to explore PD. We describe the cell source, culture conditions, differentiation protocols, methods/approaches used to mimic PD and the preclinical validation of the SH-SY5Y findings by employing alternative cellular and animal models. Thus, this overview may help to standardize the use of the SH-SY5Y cell line in PD research and serve as a future user’s guide. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13024-017-0149-0) contains supplementary material, which is available to authorized users. BioMed Central 2017-01-24 /pmc/articles/PMC5259880/ /pubmed/28118852 http://dx.doi.org/10.1186/s13024-017-0149-0 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Review Xicoy, Helena Wieringa, Bé Martens, Gerard J.M. The SH-SY5Y cell line in Parkinson’s disease research: a systematic review |
title | The SH-SY5Y cell line in Parkinson’s disease research: a systematic review |
title_full | The SH-SY5Y cell line in Parkinson’s disease research: a systematic review |
title_fullStr | The SH-SY5Y cell line in Parkinson’s disease research: a systematic review |
title_full_unstemmed | The SH-SY5Y cell line in Parkinson’s disease research: a systematic review |
title_short | The SH-SY5Y cell line in Parkinson’s disease research: a systematic review |
title_sort | sh-sy5y cell line in parkinson’s disease research: a systematic review |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5259880/ https://www.ncbi.nlm.nih.gov/pubmed/28118852 http://dx.doi.org/10.1186/s13024-017-0149-0 |
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