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Messenger RNAs localized to distal projections of human stem cell derived neurons

The identification of mRNAs in distal projections of model organisms has led to the discovery of multiple proteins that are locally synthesized for functional roles such as axon guidance, injury signaling and regeneration. The extent to which local protein synthesis is conserved in human neurons is...

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Autores principales: Bigler, Rebecca L., Kamande, Joyce W., Dumitru, Raluca, Niedringhaus, Mark, Taylor, Anne Marion
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5428799/
https://www.ncbi.nlm.nih.gov/pubmed/28377585
http://dx.doi.org/10.1038/s41598-017-00676-w
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author Bigler, Rebecca L.
Kamande, Joyce W.
Dumitru, Raluca
Niedringhaus, Mark
Taylor, Anne Marion
author_facet Bigler, Rebecca L.
Kamande, Joyce W.
Dumitru, Raluca
Niedringhaus, Mark
Taylor, Anne Marion
author_sort Bigler, Rebecca L.
collection PubMed
description The identification of mRNAs in distal projections of model organisms has led to the discovery of multiple proteins that are locally synthesized for functional roles such as axon guidance, injury signaling and regeneration. The extent to which local protein synthesis is conserved in human neurons is unknown. Here we used compartmentalized microfluidic chambers to characterize the transcriptome of distal projections of human embryonic stem cells differentiated using a protocol which enriched for glutamatergic neurons (hESC-neurons). Using gene expression analysis, we identified mRNAs proportionally enriched in these projections, representing a functionally unique local transcriptome as compared to the human neuronal transcriptome inclusive of somata. Further, we found that the most abundant mRNAs within these hESC-neuron projections were functionally similar to the axonal transcriptome of rat cortical neurons. We confirmed the presence of two well characterized axonal mRNAs in model organisms, β-actin and GAP43, within hESC-neuron projections using multiplexed single molecule RNA-FISH. Additionally, we report the novel finding that oxytocin mRNA localized to these human projections and confirmed its localization using RNA-FISH. This new evaluation of mRNA within human projections provides an important resource for studying local mRNA translation and has the potential to reveal both conserved and unique translation dependent mechanisms.
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spelling pubmed-54287992017-05-15 Messenger RNAs localized to distal projections of human stem cell derived neurons Bigler, Rebecca L. Kamande, Joyce W. Dumitru, Raluca Niedringhaus, Mark Taylor, Anne Marion Sci Rep Article The identification of mRNAs in distal projections of model organisms has led to the discovery of multiple proteins that are locally synthesized for functional roles such as axon guidance, injury signaling and regeneration. The extent to which local protein synthesis is conserved in human neurons is unknown. Here we used compartmentalized microfluidic chambers to characterize the transcriptome of distal projections of human embryonic stem cells differentiated using a protocol which enriched for glutamatergic neurons (hESC-neurons). Using gene expression analysis, we identified mRNAs proportionally enriched in these projections, representing a functionally unique local transcriptome as compared to the human neuronal transcriptome inclusive of somata. Further, we found that the most abundant mRNAs within these hESC-neuron projections were functionally similar to the axonal transcriptome of rat cortical neurons. We confirmed the presence of two well characterized axonal mRNAs in model organisms, β-actin and GAP43, within hESC-neuron projections using multiplexed single molecule RNA-FISH. Additionally, we report the novel finding that oxytocin mRNA localized to these human projections and confirmed its localization using RNA-FISH. This new evaluation of mRNA within human projections provides an important resource for studying local mRNA translation and has the potential to reveal both conserved and unique translation dependent mechanisms. Nature Publishing Group UK 2017-04-04 /pmc/articles/PMC5428799/ /pubmed/28377585 http://dx.doi.org/10.1038/s41598-017-00676-w Text en © The Author(s) 2017 This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Bigler, Rebecca L.
Kamande, Joyce W.
Dumitru, Raluca
Niedringhaus, Mark
Taylor, Anne Marion
Messenger RNAs localized to distal projections of human stem cell derived neurons
title Messenger RNAs localized to distal projections of human stem cell derived neurons
title_full Messenger RNAs localized to distal projections of human stem cell derived neurons
title_fullStr Messenger RNAs localized to distal projections of human stem cell derived neurons
title_full_unstemmed Messenger RNAs localized to distal projections of human stem cell derived neurons
title_short Messenger RNAs localized to distal projections of human stem cell derived neurons
title_sort messenger rnas localized to distal projections of human stem cell derived neurons
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5428799/
https://www.ncbi.nlm.nih.gov/pubmed/28377585
http://dx.doi.org/10.1038/s41598-017-00676-w
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