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Extracellular vesicles from neurons promote neural induction of stem cells through cyclin D1

Extracellular vesicles (EVs) are thought to mediate the transport of proteins and RNAs involved in intercellular communication. Here, we show dynamic changes in the buoyant density and abundance of EVs that are secreted by PC12 cells stimulated with nerve growth factor (NGF), N2A cells treated with...

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Detalles Bibliográficos
Autores principales: Song, Lu, Tian, Xinran, Schekman, Randy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Rockefeller University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8313409/
https://www.ncbi.nlm.nih.gov/pubmed/34309628
http://dx.doi.org/10.1083/jcb.202101075
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author Song, Lu
Tian, Xinran
Schekman, Randy
author_facet Song, Lu
Tian, Xinran
Schekman, Randy
author_sort Song, Lu
collection PubMed
description Extracellular vesicles (EVs) are thought to mediate the transport of proteins and RNAs involved in intercellular communication. Here, we show dynamic changes in the buoyant density and abundance of EVs that are secreted by PC12 cells stimulated with nerve growth factor (NGF), N2A cells treated with retinoic acid to induce neural differentiation, and mouse embryonic stem cells (mESCs) differentiated into neuronal cells. EVs secreted from in vitro differentiated cells promote neural induction of mESCs. Cyclin D1 enriched within the EVs derived from differentiated neuronal cells contributes to this induction. EVs purified from cells overexpressing cyclin D1 are more potent in neural induction of mESC cells. Depletion of cyclin D1 from the EVs reduced the neural induction effect. Our results suggest that EVs regulate neural development through sorting of cyclin D1.
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spelling pubmed-83134092021-08-05 Extracellular vesicles from neurons promote neural induction of stem cells through cyclin D1 Song, Lu Tian, Xinran Schekman, Randy J Cell Biol Article Extracellular vesicles (EVs) are thought to mediate the transport of proteins and RNAs involved in intercellular communication. Here, we show dynamic changes in the buoyant density and abundance of EVs that are secreted by PC12 cells stimulated with nerve growth factor (NGF), N2A cells treated with retinoic acid to induce neural differentiation, and mouse embryonic stem cells (mESCs) differentiated into neuronal cells. EVs secreted from in vitro differentiated cells promote neural induction of mESCs. Cyclin D1 enriched within the EVs derived from differentiated neuronal cells contributes to this induction. EVs purified from cells overexpressing cyclin D1 are more potent in neural induction of mESC cells. Depletion of cyclin D1 from the EVs reduced the neural induction effect. Our results suggest that EVs regulate neural development through sorting of cyclin D1. Rockefeller University Press 2021-07-26 /pmc/articles/PMC8313409/ /pubmed/34309628 http://dx.doi.org/10.1083/jcb.202101075 Text en © 2021 Song et al. https://creativecommons.org/licenses/by/4.0/This article is available under a Creative Commons License (Attribution 4.0 International, as described at https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Song, Lu
Tian, Xinran
Schekman, Randy
Extracellular vesicles from neurons promote neural induction of stem cells through cyclin D1
title Extracellular vesicles from neurons promote neural induction of stem cells through cyclin D1
title_full Extracellular vesicles from neurons promote neural induction of stem cells through cyclin D1
title_fullStr Extracellular vesicles from neurons promote neural induction of stem cells through cyclin D1
title_full_unstemmed Extracellular vesicles from neurons promote neural induction of stem cells through cyclin D1
title_short Extracellular vesicles from neurons promote neural induction of stem cells through cyclin D1
title_sort extracellular vesicles from neurons promote neural induction of stem cells through cyclin d1
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8313409/
https://www.ncbi.nlm.nih.gov/pubmed/34309628
http://dx.doi.org/10.1083/jcb.202101075
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