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Recent Advances: Decoding Alzheimer’s Disease With Stem Cells

Alzheimer’s disease (AD) is an irreversible neurodegenerative disorder that destroys cognitive functions. Recently, a number of high-profile clinical trials based on the amyloid cascade hypothesis have encountered disappointing results. The failure of these trials indicates the necessity for novel t...

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Detalles Bibliográficos
Autores principales: Fang, Yi, Gao, Ting, Zhang, Baorong, Pu, Jiali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5874773/
https://www.ncbi.nlm.nih.gov/pubmed/29623038
http://dx.doi.org/10.3389/fnagi.2018.00077
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author Fang, Yi
Gao, Ting
Zhang, Baorong
Pu, Jiali
author_facet Fang, Yi
Gao, Ting
Zhang, Baorong
Pu, Jiali
author_sort Fang, Yi
collection PubMed
description Alzheimer’s disease (AD) is an irreversible neurodegenerative disorder that destroys cognitive functions. Recently, a number of high-profile clinical trials based on the amyloid cascade hypothesis have encountered disappointing results. The failure of these trials indicates the necessity for novel therapeutic strategies and disease models. In this review, we will describe how recent advances in stem cell technology have shed light on a novel treatment strategy and revolutionized the mechanistic investigation of AD pathogenesis. Current advances in promoting endogenous neurogenesis and transplanting exogenous stem cells from both bench research and clinical translation perspectives will be thoroughly summarized. In addition, reprogramming technology-based disease modeling, which has shown improved efficacy in recapitulating pathological features in human patients, will be discussed.
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spelling pubmed-58747732018-04-05 Recent Advances: Decoding Alzheimer’s Disease With Stem Cells Fang, Yi Gao, Ting Zhang, Baorong Pu, Jiali Front Aging Neurosci Neuroscience Alzheimer’s disease (AD) is an irreversible neurodegenerative disorder that destroys cognitive functions. Recently, a number of high-profile clinical trials based on the amyloid cascade hypothesis have encountered disappointing results. The failure of these trials indicates the necessity for novel therapeutic strategies and disease models. In this review, we will describe how recent advances in stem cell technology have shed light on a novel treatment strategy and revolutionized the mechanistic investigation of AD pathogenesis. Current advances in promoting endogenous neurogenesis and transplanting exogenous stem cells from both bench research and clinical translation perspectives will be thoroughly summarized. In addition, reprogramming technology-based disease modeling, which has shown improved efficacy in recapitulating pathological features in human patients, will be discussed. Frontiers Media S.A. 2018-03-22 /pmc/articles/PMC5874773/ /pubmed/29623038 http://dx.doi.org/10.3389/fnagi.2018.00077 Text en Copyright © 2018 Fang, Gao, Zhang and Pu. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Fang, Yi
Gao, Ting
Zhang, Baorong
Pu, Jiali
Recent Advances: Decoding Alzheimer’s Disease With Stem Cells
title Recent Advances: Decoding Alzheimer’s Disease With Stem Cells
title_full Recent Advances: Decoding Alzheimer’s Disease With Stem Cells
title_fullStr Recent Advances: Decoding Alzheimer’s Disease With Stem Cells
title_full_unstemmed Recent Advances: Decoding Alzheimer’s Disease With Stem Cells
title_short Recent Advances: Decoding Alzheimer’s Disease With Stem Cells
title_sort recent advances: decoding alzheimer’s disease with stem cells
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5874773/
https://www.ncbi.nlm.nih.gov/pubmed/29623038
http://dx.doi.org/10.3389/fnagi.2018.00077
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