Using Human iPSC-Derived Neurons to Uncover Activity-Dependent Non-Coding RNAs

Humans are arguably the most complex organisms present on Earth with their ability to imagine, create, and problem solve. As underlying mechanisms enabling these capacities reside in the brain, it is not surprising that the brain has undergone an extraordinary increase in size and complexity within...

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Main Authors: Mainá Bitar, Stefanie Kuiper, Elizabeth O’Brien, Guy Barry
Format: Article
Language:English
Published: MDPI AG 2017-12-01
Series:Genes
Subjects:
Online Access:https://www.mdpi.com/2073-4425/8/12/401
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spelling doaj-fc26407b26c94b80bf69e79c06501bea2020-11-24T22:05:33ZengMDPI AGGenes2073-44252017-12-0181240110.3390/genes8120401genes8120401Using Human iPSC-Derived Neurons to Uncover Activity-Dependent Non-Coding RNAsMainá Bitar0Stefanie Kuiper1Elizabeth O’Brien2Guy Barry3QIMR Berghofer Medical Research Institute, Herston, QLD 4006, AustraliaQIMR Berghofer Medical Research Institute, Herston, QLD 4006, AustraliaQIMR Berghofer Medical Research Institute, Herston, QLD 4006, AustraliaQIMR Berghofer Medical Research Institute, Herston, QLD 4006, AustraliaHumans are arguably the most complex organisms present on Earth with their ability to imagine, create, and problem solve. As underlying mechanisms enabling these capacities reside in the brain, it is not surprising that the brain has undergone an extraordinary increase in size and complexity within the last few million years. Human induced pluripotent stem cells (hiPSCs) can be differentiated into many cell types that were virtually inaccessible historically, such as neurons. Here, we used hiPSC-derived neurons to investigate the cellular response to activation at the transcript level. Neuronal activation was performed with potassium chloride (KCl) and its effects were assessed by RNA sequencing. Our results revealed the involvement of long non-coding RNAs and human-specific genetic variants in response to neuronal activation and help validate hiPSCs as a valuable resource for the study of human neuronal networks. In summary, we find that genes affected by KCl-triggered activation are implicated in pathways that drive cell proliferation, differentiation, and the emergence of specialized morphological features. Interestingly, non-coding RNAs of various classes are amongst the most highly expressed genes in activated hiPSC-derived neurons, thus suggesting these play crucial roles in neural pathways and may significantly contribute to the unique functioning of the human brain.https://www.mdpi.com/2073-4425/8/12/401iPSCstem cellsneuronsnon-coding RNAneuronal activationhuman-specificRNA-Seq
collection DOAJ
language English
format Article
sources DOAJ
author Mainá Bitar
Stefanie Kuiper
Elizabeth O’Brien
Guy Barry
spellingShingle Mainá Bitar
Stefanie Kuiper
Elizabeth O’Brien
Guy Barry
Using Human iPSC-Derived Neurons to Uncover Activity-Dependent Non-Coding RNAs
Genes
iPSC
stem cells
neurons
non-coding RNA
neuronal activation
human-specific
RNA-Seq
author_facet Mainá Bitar
Stefanie Kuiper
Elizabeth O’Brien
Guy Barry
author_sort Mainá Bitar
title Using Human iPSC-Derived Neurons to Uncover Activity-Dependent Non-Coding RNAs
title_short Using Human iPSC-Derived Neurons to Uncover Activity-Dependent Non-Coding RNAs
title_full Using Human iPSC-Derived Neurons to Uncover Activity-Dependent Non-Coding RNAs
title_fullStr Using Human iPSC-Derived Neurons to Uncover Activity-Dependent Non-Coding RNAs
title_full_unstemmed Using Human iPSC-Derived Neurons to Uncover Activity-Dependent Non-Coding RNAs
title_sort using human ipsc-derived neurons to uncover activity-dependent non-coding rnas
publisher MDPI AG
series Genes
issn 2073-4425
publishDate 2017-12-01
description Humans are arguably the most complex organisms present on Earth with their ability to imagine, create, and problem solve. As underlying mechanisms enabling these capacities reside in the brain, it is not surprising that the brain has undergone an extraordinary increase in size and complexity within the last few million years. Human induced pluripotent stem cells (hiPSCs) can be differentiated into many cell types that were virtually inaccessible historically, such as neurons. Here, we used hiPSC-derived neurons to investigate the cellular response to activation at the transcript level. Neuronal activation was performed with potassium chloride (KCl) and its effects were assessed by RNA sequencing. Our results revealed the involvement of long non-coding RNAs and human-specific genetic variants in response to neuronal activation and help validate hiPSCs as a valuable resource for the study of human neuronal networks. In summary, we find that genes affected by KCl-triggered activation are implicated in pathways that drive cell proliferation, differentiation, and the emergence of specialized morphological features. Interestingly, non-coding RNAs of various classes are amongst the most highly expressed genes in activated hiPSC-derived neurons, thus suggesting these play crucial roles in neural pathways and may significantly contribute to the unique functioning of the human brain.
topic iPSC
stem cells
neurons
non-coding RNA
neuronal activation
human-specific
RNA-Seq
url https://www.mdpi.com/2073-4425/8/12/401
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