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Treating Parkinson’s disease in the 21st century: Can stem cell transplantation compete?

The characteristic and selective degeneration of a unique population of cells—the nigrostriatal dopamine (DA) neurons—that occurs in Parkinson’s disease (PD) has made the condition an iconic target for cell replacement therapies. Indeed, transplantation of fetal ventral mesencephalic cells into the...

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Detalles Bibliográficos
Autores principales: Buttery, Philip C, Barker, Roger A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BlackWell Publishing Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4233918/
https://www.ncbi.nlm.nih.gov/pubmed/24610597
http://dx.doi.org/10.1002/cne.23577
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author Buttery, Philip C
Barker, Roger A
author_facet Buttery, Philip C
Barker, Roger A
author_sort Buttery, Philip C
collection PubMed
description The characteristic and selective degeneration of a unique population of cells—the nigrostriatal dopamine (DA) neurons—that occurs in Parkinson’s disease (PD) has made the condition an iconic target for cell replacement therapies. Indeed, transplantation of fetal ventral mesencephalic cells into the DA-deficient striatum was first trialled nearly 30 years ago, at a time when other treatments for the disease were less well developed. Over recent decades standard treatments for PD have advanced, and newer biological therapies are now emerging. In the 21st century, stem cell technology will have to compete alongside other sophisticated treatments, including deep brain stimulation and gene therapies. In this review we examine how stem cell–based transplantation therapies compare with these novel and emerging treatments in the management of this common condition. J. Comp. Neurol. 522:2802–2816, 2014.
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spelling pubmed-42339182014-12-03 Treating Parkinson’s disease in the 21st century: Can stem cell transplantation compete? Buttery, Philip C Barker, Roger A J Comp Neurol Reviews The characteristic and selective degeneration of a unique population of cells—the nigrostriatal dopamine (DA) neurons—that occurs in Parkinson’s disease (PD) has made the condition an iconic target for cell replacement therapies. Indeed, transplantation of fetal ventral mesencephalic cells into the DA-deficient striatum was first trialled nearly 30 years ago, at a time when other treatments for the disease were less well developed. Over recent decades standard treatments for PD have advanced, and newer biological therapies are now emerging. In the 21st century, stem cell technology will have to compete alongside other sophisticated treatments, including deep brain stimulation and gene therapies. In this review we examine how stem cell–based transplantation therapies compare with these novel and emerging treatments in the management of this common condition. J. Comp. Neurol. 522:2802–2816, 2014. BlackWell Publishing Ltd 2014-01-01 2014-01-01 /pmc/articles/PMC4233918/ /pubmed/24610597 http://dx.doi.org/10.1002/cne.23577 Text en © 2014 Wiley Periodicals, Inc. http://creativecommons.org/licenses/by-nc/3.0/ This is an open access article under the terms of the Creative Commons Attribution-NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Reviews
Buttery, Philip C
Barker, Roger A
Treating Parkinson’s disease in the 21st century: Can stem cell transplantation compete?
title Treating Parkinson’s disease in the 21st century: Can stem cell transplantation compete?
title_full Treating Parkinson’s disease in the 21st century: Can stem cell transplantation compete?
title_fullStr Treating Parkinson’s disease in the 21st century: Can stem cell transplantation compete?
title_full_unstemmed Treating Parkinson’s disease in the 21st century: Can stem cell transplantation compete?
title_short Treating Parkinson’s disease in the 21st century: Can stem cell transplantation compete?
title_sort treating parkinson’s disease in the 21st century: can stem cell transplantation compete?
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4233918/
https://www.ncbi.nlm.nih.gov/pubmed/24610597
http://dx.doi.org/10.1002/cne.23577
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