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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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 |
work_keys_str_mv |
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1721218332275769344 |