Emerging hiPSC Models for Drug Discovery in Neurodegenerative Diseases

Neurodegenerative diseases affect millions of people worldwide and are characterized by the chronic and progressive deterioration of neural function. Neurodegenerative diseases, such as Alzheimer’s disease (AD), Parkinson’s disease (PD), amyotrophic lateral sclerosis (ALS), and Huntington’s disease...

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Main Authors: Dorit Trudler, Swagata Ghatak, Stuart A. Lipton
Format: Article
Language:English
Published: MDPI AG 2021-07-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/22/15/8196
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spelling doaj-f1fc9977e8fe4be7bfec6cad7d70e13b2021-08-06T15:25:51ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672021-07-01228196819610.3390/ijms22158196Emerging hiPSC Models for Drug Discovery in Neurodegenerative DiseasesDorit Trudler0Swagata Ghatak1Stuart A. Lipton2Neurodegeneration New Medicines Center and Department of Molecular Medicine, The Scripps Research Institute, La Jolla, CA 92037, USANeurodegeneration New Medicines Center and Department of Molecular Medicine, The Scripps Research Institute, La Jolla, CA 92037, USANeurodegeneration New Medicines Center and Department of Molecular Medicine, The Scripps Research Institute, La Jolla, CA 92037, USANeurodegenerative diseases affect millions of people worldwide and are characterized by the chronic and progressive deterioration of neural function. Neurodegenerative diseases, such as Alzheimer’s disease (AD), Parkinson’s disease (PD), amyotrophic lateral sclerosis (ALS), and Huntington’s disease (HD), represent a huge social and economic burden due to increasing prevalence in our aging society, severity of symptoms, and lack of effective disease-modifying therapies. This lack of effective treatments is partly due to a lack of reliable models. Modeling neurodegenerative diseases is difficult because of poor access to human samples (restricted in general to postmortem tissue) and limited knowledge of disease mechanisms in a human context. Animal models play an instrumental role in understanding these diseases but fail to comprehensively represent the full extent of disease due to critical differences between humans and other mammals. The advent of human-induced pluripotent stem cell (hiPSC) technology presents an advantageous system that complements animal models of neurodegenerative diseases. Coupled with advances in gene-editing technologies, hiPSC-derived neural cells from patients and healthy donors now allow disease modeling using human samples that can be used for drug discovery.https://www.mdpi.com/1422-0067/22/15/8196neurodegenerationAlzheimer’s disease
collection DOAJ
language English
format Article
sources DOAJ
author Dorit Trudler
Swagata Ghatak
Stuart A. Lipton
spellingShingle Dorit Trudler
Swagata Ghatak
Stuart A. Lipton
Emerging hiPSC Models for Drug Discovery in Neurodegenerative Diseases
International Journal of Molecular Sciences
neurodegeneration
Alzheimer’s disease
author_facet Dorit Trudler
Swagata Ghatak
Stuart A. Lipton
author_sort Dorit Trudler
title Emerging hiPSC Models for Drug Discovery in Neurodegenerative Diseases
title_short Emerging hiPSC Models for Drug Discovery in Neurodegenerative Diseases
title_full Emerging hiPSC Models for Drug Discovery in Neurodegenerative Diseases
title_fullStr Emerging hiPSC Models for Drug Discovery in Neurodegenerative Diseases
title_full_unstemmed Emerging hiPSC Models for Drug Discovery in Neurodegenerative Diseases
title_sort emerging hipsc models for drug discovery in neurodegenerative diseases
publisher MDPI AG
series International Journal of Molecular Sciences
issn 1661-6596
1422-0067
publishDate 2021-07-01
description Neurodegenerative diseases affect millions of people worldwide and are characterized by the chronic and progressive deterioration of neural function. Neurodegenerative diseases, such as Alzheimer’s disease (AD), Parkinson’s disease (PD), amyotrophic lateral sclerosis (ALS), and Huntington’s disease (HD), represent a huge social and economic burden due to increasing prevalence in our aging society, severity of symptoms, and lack of effective disease-modifying therapies. This lack of effective treatments is partly due to a lack of reliable models. Modeling neurodegenerative diseases is difficult because of poor access to human samples (restricted in general to postmortem tissue) and limited knowledge of disease mechanisms in a human context. Animal models play an instrumental role in understanding these diseases but fail to comprehensively represent the full extent of disease due to critical differences between humans and other mammals. The advent of human-induced pluripotent stem cell (hiPSC) technology presents an advantageous system that complements animal models of neurodegenerative diseases. Coupled with advances in gene-editing technologies, hiPSC-derived neural cells from patients and healthy donors now allow disease modeling using human samples that can be used for drug discovery.
topic neurodegeneration
Alzheimer’s disease
url https://www.mdpi.com/1422-0067/22/15/8196
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