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The role of induced pluripotent stem cells in regenerative medicine: neurodegenerative diseases

Alzheimer's disease, Parkinson's disease, Huntington's disease, amyotrophic lateral sclerosis, and Friedreich's ataxia are the most common human neurodegenerative diseases pathologically characterized by a progressive and specific loss of certain neuronal populations. The exact m...

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Detalles Bibliográficos
Autores principales: Peng, Jun, Zeng, Xianmin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3219063/
https://www.ncbi.nlm.nih.gov/pubmed/21861938
http://dx.doi.org/10.1186/scrt73
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author Peng, Jun
Zeng, Xianmin
author_facet Peng, Jun
Zeng, Xianmin
author_sort Peng, Jun
collection PubMed
description Alzheimer's disease, Parkinson's disease, Huntington's disease, amyotrophic lateral sclerosis, and Friedreich's ataxia are the most common human neurodegenerative diseases pathologically characterized by a progressive and specific loss of certain neuronal populations. The exact mechanisms of neuronal cell death in these diseases are unclear, although some forms of the diseases are inherited and genes causing these diseases have been identified. Currently there are no effective clinical therapies for many of these diseases. The recently acquired ability to reprogram human adult somatic cells to induced pluripotent stem cells (iPSCs) in culture may provide a powerful tool for in vitro neurodegenerative disease modeling and an unlimited source for cell replacement therapy. In the present review, we summarize recent progress on iPSC generation and differentiation into neuronal cell types and discuss the potential application for in vitro disease mechanism study and in vivo cell replacement therapy.
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spelling pubmed-32190632012-07-28 The role of induced pluripotent stem cells in regenerative medicine: neurodegenerative diseases Peng, Jun Zeng, Xianmin Stem Cell Res Ther Review Alzheimer's disease, Parkinson's disease, Huntington's disease, amyotrophic lateral sclerosis, and Friedreich's ataxia are the most common human neurodegenerative diseases pathologically characterized by a progressive and specific loss of certain neuronal populations. The exact mechanisms of neuronal cell death in these diseases are unclear, although some forms of the diseases are inherited and genes causing these diseases have been identified. Currently there are no effective clinical therapies for many of these diseases. The recently acquired ability to reprogram human adult somatic cells to induced pluripotent stem cells (iPSCs) in culture may provide a powerful tool for in vitro neurodegenerative disease modeling and an unlimited source for cell replacement therapy. In the present review, we summarize recent progress on iPSC generation and differentiation into neuronal cell types and discuss the potential application for in vitro disease mechanism study and in vivo cell replacement therapy. BioMed Central 2011-07-28 /pmc/articles/PMC3219063/ /pubmed/21861938 http://dx.doi.org/10.1186/scrt73 Text en Copyright ©2011 BioMed Central Ltd
spellingShingle Review
Peng, Jun
Zeng, Xianmin
The role of induced pluripotent stem cells in regenerative medicine: neurodegenerative diseases
title The role of induced pluripotent stem cells in regenerative medicine: neurodegenerative diseases
title_full The role of induced pluripotent stem cells in regenerative medicine: neurodegenerative diseases
title_fullStr The role of induced pluripotent stem cells in regenerative medicine: neurodegenerative diseases
title_full_unstemmed The role of induced pluripotent stem cells in regenerative medicine: neurodegenerative diseases
title_short The role of induced pluripotent stem cells in regenerative medicine: neurodegenerative diseases
title_sort role of induced pluripotent stem cells in regenerative medicine: neurodegenerative diseases
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3219063/
https://www.ncbi.nlm.nih.gov/pubmed/21861938
http://dx.doi.org/10.1186/scrt73
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