Precision modulation of neurodegenerative disease-related gene expression in human iPSC-derived neurons

The ability to reprogram adult somatic cells into induced pluripotent stem cells (iPSCs) and the subsequent development of protocols for their differentiation into disease-relevant cell types have enabled in-depth molecular analyses of multiple disease states as hitherto impossible. Neurons differen...

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Główni autorzy: Heman-Ackah, S, Bassett, A, Wood, M
Format: Journal article
Wydane: Springer Nature 2016
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author Heman-Ackah, S
Bassett, A
Wood, M
author_facet Heman-Ackah, S
Bassett, A
Wood, M
author_sort Heman-Ackah, S
collection OXFORD
description The ability to reprogram adult somatic cells into induced pluripotent stem cells (iPSCs) and the subsequent development of protocols for their differentiation into disease-relevant cell types have enabled in-depth molecular analyses of multiple disease states as hitherto impossible. Neurons differentiated from patient-specific iPSCs provide a means to recapitulate molecular phenotypes of neurodegenerative diseases in vitro. However, it remains challenging to conduct precise manipulations of gene expression in iPSC-derived neurons towards modeling complex human neurological diseases. The application of CRISPR/Cas9 to mammalian systems is revolutionizing the utilization of genome editing technologies in the study of molecular contributors to the pathogenesis of numerous diseases. Here, we demonstrate that CRISPRa and CRISPRi can be used to exert precise modulations of endogenous gene expression in fate-committed iPSC-derived neurons. This highlights CRISPRa/i as a major technical advancement in accessible tools for evaluating the specific contributions of critical neurodegenerative disease-related genes to neuropathogenesis.
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spelling oxford-uuid:c5f6c94b-6598-41f8-ae4c-28b37d9afc2a2022-03-27T06:34:51ZPrecision modulation of neurodegenerative disease-related gene expression in human iPSC-derived neuronsJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:c5f6c94b-6598-41f8-ae4c-28b37d9afc2aSymplectic Elements at OxfordSpringer Nature2016Heman-Ackah, SBassett, AWood, MThe ability to reprogram adult somatic cells into induced pluripotent stem cells (iPSCs) and the subsequent development of protocols for their differentiation into disease-relevant cell types have enabled in-depth molecular analyses of multiple disease states as hitherto impossible. Neurons differentiated from patient-specific iPSCs provide a means to recapitulate molecular phenotypes of neurodegenerative diseases in vitro. However, it remains challenging to conduct precise manipulations of gene expression in iPSC-derived neurons towards modeling complex human neurological diseases. The application of CRISPR/Cas9 to mammalian systems is revolutionizing the utilization of genome editing technologies in the study of molecular contributors to the pathogenesis of numerous diseases. Here, we demonstrate that CRISPRa and CRISPRi can be used to exert precise modulations of endogenous gene expression in fate-committed iPSC-derived neurons. This highlights CRISPRa/i as a major technical advancement in accessible tools for evaluating the specific contributions of critical neurodegenerative disease-related genes to neuropathogenesis.
spellingShingle Heman-Ackah, S
Bassett, A
Wood, M
Precision modulation of neurodegenerative disease-related gene expression in human iPSC-derived neurons
title Precision modulation of neurodegenerative disease-related gene expression in human iPSC-derived neurons
title_full Precision modulation of neurodegenerative disease-related gene expression in human iPSC-derived neurons
title_fullStr Precision modulation of neurodegenerative disease-related gene expression in human iPSC-derived neurons
title_full_unstemmed Precision modulation of neurodegenerative disease-related gene expression in human iPSC-derived neurons
title_short Precision modulation of neurodegenerative disease-related gene expression in human iPSC-derived neurons
title_sort precision modulation of neurodegenerative disease related gene expression in human ipsc derived neurons
work_keys_str_mv AT hemanackahs precisionmodulationofneurodegenerativediseaserelatedgeneexpressioninhumanipscderivedneurons
AT bassetta precisionmodulationofneurodegenerativediseaserelatedgeneexpressioninhumanipscderivedneurons
AT woodm precisionmodulationofneurodegenerativediseaserelatedgeneexpressioninhumanipscderivedneurons