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Quantitative comparison of the mRNA content of human iPSC‐derived motor neurons and their extracellular vesicles
Extracellular vesicles (EVs) contain various cargo molecules, including RNAs and proteins. EVs, which include exosomes, are predicted to be suitable surrogates of their source cells for liquid biopsy to measure biomarkers. Several studies have performed qualitative comparisons of cargo molecule repe...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7876496/ https://www.ncbi.nlm.nih.gov/pubmed/33296136 http://dx.doi.org/10.1002/2211-5463.13059 |
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author | Otake, Kentaro Adachi‐Tominari, Keiko Nagai, Hiroaki Saito, Masayo Sano, Osamu Hirozane, Yoshihiko Iwata, Hidehisa |
author_facet | Otake, Kentaro Adachi‐Tominari, Keiko Nagai, Hiroaki Saito, Masayo Sano, Osamu Hirozane, Yoshihiko Iwata, Hidehisa |
author_sort | Otake, Kentaro |
collection | PubMed |
description | Extracellular vesicles (EVs) contain various cargo molecules, including RNAs and proteins. EVs, which include exosomes, are predicted to be suitable surrogates of their source cells for liquid biopsy to measure biomarkers. Several studies have performed qualitative comparisons of cargo molecule repertoires between source cells and their EVs. However, quantitative comparisons have not been reported so far. Furthermore, many studies analyzed microRNAs or proteins in EVs, but not mRNAs. In this study, we analyzed mRNAs in motor neurons and their EVs. Normal human‐induced pluripotent stem cells were differentiated into motor neurons, and comprehensive analysis of mRNAs in the cells and their EVs was performed by RNA sequencing. Differential analysis between cellular and EV mRNAs was performed by edgeR after normalization of read count. The results suggest that signatures in the abundance of EV mRNAs were different from those of cellular mRNAs. Comparison of intracellular vesicle and EV mRNA abundance showed negatively and positively biased genes in the EVs. Gene Ontology analysis revealed that the genes showing negatively biased abundance in the EVs were enriched in many functions regarding neuronal development. In contrast, the positively biased genes were enriched in functions regarding cellular metabolism and protein synthesis. These results suggest that mRNAs in motor neurons are loaded into EVs to regulate certain mechanisms, which are yet to be elucidated. |
format | Online Article Text |
id | pubmed-7876496 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-78764962021-02-18 Quantitative comparison of the mRNA content of human iPSC‐derived motor neurons and their extracellular vesicles Otake, Kentaro Adachi‐Tominari, Keiko Nagai, Hiroaki Saito, Masayo Sano, Osamu Hirozane, Yoshihiko Iwata, Hidehisa FEBS Open Bio Research Articles Extracellular vesicles (EVs) contain various cargo molecules, including RNAs and proteins. EVs, which include exosomes, are predicted to be suitable surrogates of their source cells for liquid biopsy to measure biomarkers. Several studies have performed qualitative comparisons of cargo molecule repertoires between source cells and their EVs. However, quantitative comparisons have not been reported so far. Furthermore, many studies analyzed microRNAs or proteins in EVs, but not mRNAs. In this study, we analyzed mRNAs in motor neurons and their EVs. Normal human‐induced pluripotent stem cells were differentiated into motor neurons, and comprehensive analysis of mRNAs in the cells and their EVs was performed by RNA sequencing. Differential analysis between cellular and EV mRNAs was performed by edgeR after normalization of read count. The results suggest that signatures in the abundance of EV mRNAs were different from those of cellular mRNAs. Comparison of intracellular vesicle and EV mRNA abundance showed negatively and positively biased genes in the EVs. Gene Ontology analysis revealed that the genes showing negatively biased abundance in the EVs were enriched in many functions regarding neuronal development. In contrast, the positively biased genes were enriched in functions regarding cellular metabolism and protein synthesis. These results suggest that mRNAs in motor neurons are loaded into EVs to regulate certain mechanisms, which are yet to be elucidated. John Wiley and Sons Inc. 2021-02-02 /pmc/articles/PMC7876496/ /pubmed/33296136 http://dx.doi.org/10.1002/2211-5463.13059 Text en © 2020 Takeda Pharmaceutical Company Ltd. FEBS Open Bio published by John Wiley & Sons Ltd on behalf of Federation of European Biochemical Societies. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Otake, Kentaro Adachi‐Tominari, Keiko Nagai, Hiroaki Saito, Masayo Sano, Osamu Hirozane, Yoshihiko Iwata, Hidehisa Quantitative comparison of the mRNA content of human iPSC‐derived motor neurons and their extracellular vesicles |
title | Quantitative comparison of the mRNA content of human iPSC‐derived motor neurons and their extracellular vesicles |
title_full | Quantitative comparison of the mRNA content of human iPSC‐derived motor neurons and their extracellular vesicles |
title_fullStr | Quantitative comparison of the mRNA content of human iPSC‐derived motor neurons and their extracellular vesicles |
title_full_unstemmed | Quantitative comparison of the mRNA content of human iPSC‐derived motor neurons and their extracellular vesicles |
title_short | Quantitative comparison of the mRNA content of human iPSC‐derived motor neurons and their extracellular vesicles |
title_sort | quantitative comparison of the mrna content of human ipsc‐derived motor neurons and their extracellular vesicles |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7876496/ https://www.ncbi.nlm.nih.gov/pubmed/33296136 http://dx.doi.org/10.1002/2211-5463.13059 |
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