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Opportunities and Limitations of Modelling Alzheimer’s Disease with Induced Pluripotent Stem Cells

Reprogramming of somatic cells into induced pluripotent stem cells (iPSCs) has opened the way for patient-specific disease modelling. Following their differentiation into neuronal cell types, iPSC have enabled the investigation of human neurodegenerative diseases, such as Alzheimer’s disease (AD). W...

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Detalles Bibliográficos
Autores principales: Ovchinnikov, Dmitry A., Wolvetang, Ernst J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4470188/
https://www.ncbi.nlm.nih.gov/pubmed/26237606
http://dx.doi.org/10.3390/jcm3041357
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author Ovchinnikov, Dmitry A.
Wolvetang, Ernst J.
author_facet Ovchinnikov, Dmitry A.
Wolvetang, Ernst J.
author_sort Ovchinnikov, Dmitry A.
collection PubMed
description Reprogramming of somatic cells into induced pluripotent stem cells (iPSCs) has opened the way for patient-specific disease modelling. Following their differentiation into neuronal cell types, iPSC have enabled the investigation of human neurodegenerative diseases, such as Alzheimer’s disease (AD). While human iPSCs certainly provide great opportunities to repeatedly interrogate specific human brain cell types of individuals with familial and sporadic forms of the disease, the complex aetiology and timescale over which AD develops in humans poses particular challenges to iPSC-based AD models. Here, we discuss the current state-of-play in the context of these and other iPSC model-related challenges and elaborate on likely future developments in this field of research.
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spelling pubmed-44701882015-07-28 Opportunities and Limitations of Modelling Alzheimer’s Disease with Induced Pluripotent Stem Cells Ovchinnikov, Dmitry A. Wolvetang, Ernst J. J Clin Med Review Reprogramming of somatic cells into induced pluripotent stem cells (iPSCs) has opened the way for patient-specific disease modelling. Following their differentiation into neuronal cell types, iPSC have enabled the investigation of human neurodegenerative diseases, such as Alzheimer’s disease (AD). While human iPSCs certainly provide great opportunities to repeatedly interrogate specific human brain cell types of individuals with familial and sporadic forms of the disease, the complex aetiology and timescale over which AD develops in humans poses particular challenges to iPSC-based AD models. Here, we discuss the current state-of-play in the context of these and other iPSC model-related challenges and elaborate on likely future developments in this field of research. MDPI 2014-12-05 /pmc/articles/PMC4470188/ /pubmed/26237606 http://dx.doi.org/10.3390/jcm3041357 Text en © 2014 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Ovchinnikov, Dmitry A.
Wolvetang, Ernst J.
Opportunities and Limitations of Modelling Alzheimer’s Disease with Induced Pluripotent Stem Cells
title Opportunities and Limitations of Modelling Alzheimer’s Disease with Induced Pluripotent Stem Cells
title_full Opportunities and Limitations of Modelling Alzheimer’s Disease with Induced Pluripotent Stem Cells
title_fullStr Opportunities and Limitations of Modelling Alzheimer’s Disease with Induced Pluripotent Stem Cells
title_full_unstemmed Opportunities and Limitations of Modelling Alzheimer’s Disease with Induced Pluripotent Stem Cells
title_short Opportunities and Limitations of Modelling Alzheimer’s Disease with Induced Pluripotent Stem Cells
title_sort opportunities and limitations of modelling alzheimer’s disease with induced pluripotent stem cells
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4470188/
https://www.ncbi.nlm.nih.gov/pubmed/26237606
http://dx.doi.org/10.3390/jcm3041357
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