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Induced dopaminergic neurons: A new promise for Parkinson’s disease

Motor symptoms that define Parkinson’s disease (PD) are caused by the selective loss of nigral dopaminergic (DA) neurons. Cell replacement therapy for PD has been focused on midbrain DA neurons derived from human fetal mesencephalic tissue, human embryonic stem cells (hESC) or human induced pluripot...

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Autores principales: Xu, Zhimin, Chu, Xingkun, Jiang, Houbo, Schilling, Haley, Chen, Shengdi, Feng, Jian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5256671/
https://www.ncbi.nlm.nih.gov/pubmed/28110217
http://dx.doi.org/10.1016/j.redox.2017.01.009
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author Xu, Zhimin
Chu, Xingkun
Jiang, Houbo
Schilling, Haley
Chen, Shengdi
Feng, Jian
author_facet Xu, Zhimin
Chu, Xingkun
Jiang, Houbo
Schilling, Haley
Chen, Shengdi
Feng, Jian
author_sort Xu, Zhimin
collection PubMed
description Motor symptoms that define Parkinson’s disease (PD) are caused by the selective loss of nigral dopaminergic (DA) neurons. Cell replacement therapy for PD has been focused on midbrain DA neurons derived from human fetal mesencephalic tissue, human embryonic stem cells (hESC) or human induced pluripotent stem cells (iPSC). Recent development in the direct conversion of human fibroblasts to induced dopaminergic (iDA) neurons offers new opportunities for transplantation study and disease modeling in PD. The iDA neurons are generated directly from human fibroblasts in a short period of time, bypassing lengthy differentiation process from human pluripotent stem cells and the concern for potentially tumorigenic mitotic cells. They exhibit functional dopaminergic neurotransmission and relieve locomotor symptoms in animal models of Parkinson’s disease. In this review, we will discuss this recent development and its implications to Parkinson’s disease research and therapy.
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spelling pubmed-52566712017-01-30 Induced dopaminergic neurons: A new promise for Parkinson’s disease Xu, Zhimin Chu, Xingkun Jiang, Houbo Schilling, Haley Chen, Shengdi Feng, Jian Redox Biol Short Review Motor symptoms that define Parkinson’s disease (PD) are caused by the selective loss of nigral dopaminergic (DA) neurons. Cell replacement therapy for PD has been focused on midbrain DA neurons derived from human fetal mesencephalic tissue, human embryonic stem cells (hESC) or human induced pluripotent stem cells (iPSC). Recent development in the direct conversion of human fibroblasts to induced dopaminergic (iDA) neurons offers new opportunities for transplantation study and disease modeling in PD. The iDA neurons are generated directly from human fibroblasts in a short period of time, bypassing lengthy differentiation process from human pluripotent stem cells and the concern for potentially tumorigenic mitotic cells. They exhibit functional dopaminergic neurotransmission and relieve locomotor symptoms in animal models of Parkinson’s disease. In this review, we will discuss this recent development and its implications to Parkinson’s disease research and therapy. Elsevier 2017-01-16 /pmc/articles/PMC5256671/ /pubmed/28110217 http://dx.doi.org/10.1016/j.redox.2017.01.009 Text en © 2017 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Short Review
Xu, Zhimin
Chu, Xingkun
Jiang, Houbo
Schilling, Haley
Chen, Shengdi
Feng, Jian
Induced dopaminergic neurons: A new promise for Parkinson’s disease
title Induced dopaminergic neurons: A new promise for Parkinson’s disease
title_full Induced dopaminergic neurons: A new promise for Parkinson’s disease
title_fullStr Induced dopaminergic neurons: A new promise for Parkinson’s disease
title_full_unstemmed Induced dopaminergic neurons: A new promise for Parkinson’s disease
title_short Induced dopaminergic neurons: A new promise for Parkinson’s disease
title_sort induced dopaminergic neurons: a new promise for parkinson’s disease
topic Short Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5256671/
https://www.ncbi.nlm.nih.gov/pubmed/28110217
http://dx.doi.org/10.1016/j.redox.2017.01.009
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