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Extracellular vesicles derived from the choroid plexus trigger the differentiation of neural stem cells
The choroid plexus secrets cerebrospinal fluid (CSF) composed of electrolytes, cytokines, growth factors, metabolites and extracellular vesicles (EVs) that flow through the interconnected brain ventricles. On their course, CSF components can act as signals that affect, for example, neural stem cells...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9630752/ https://www.ncbi.nlm.nih.gov/pubmed/36325603 http://dx.doi.org/10.1002/jev2.12276 |
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author | Ditte, Zuzana Silbern, Ivan Ditte, Peter Urlaub, Henning Eichele, Gregor |
author_facet | Ditte, Zuzana Silbern, Ivan Ditte, Peter Urlaub, Henning Eichele, Gregor |
author_sort | Ditte, Zuzana |
collection | PubMed |
description | The choroid plexus secrets cerebrospinal fluid (CSF) composed of electrolytes, cytokines, growth factors, metabolites and extracellular vesicles (EVs) that flow through the interconnected brain ventricles. On their course, CSF components can act as signals that affect, for example, neural stem cells (NSCs) residing in niches of the ventricular wall. We studied EV‐born CSF signals in an in vitro culture system. We purified EVs from the secretome of a choroid plexus cell line (Z310 cells), and from primary choroid plexus cultures and co‐cultured those EVs with NSCs isolated from the niche of the lateral and the third ventricle. EVs(Z310) and EVs(CHP) were purified by differential centrifugation. This yielded fractions of EVs of 50–150‐nm diameter that induced a complex multicellular network formation and NSC differentiation. Both types of EV converted the round NSCs to cells that extended long processes that contacted nearby, alike‐shaped cells. Mass spectrometry showed that the differentiation‐inducing EV(Z310) were enriched for membrane and membrane‐associated proteins involved in cell differentiation, membrane trafficking, and membrane organization. We hypothesize that this type of EV (Z310) cargo causes changes of stem cell morphology that leads to multicellular networks in the niches. This cell‐shape transition may represent an initial step in NSC differentiation. |
format | Online Article Text |
id | pubmed-9630752 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-96307522022-11-07 Extracellular vesicles derived from the choroid plexus trigger the differentiation of neural stem cells Ditte, Zuzana Silbern, Ivan Ditte, Peter Urlaub, Henning Eichele, Gregor J Extracell Vesicles Research Articles The choroid plexus secrets cerebrospinal fluid (CSF) composed of electrolytes, cytokines, growth factors, metabolites and extracellular vesicles (EVs) that flow through the interconnected brain ventricles. On their course, CSF components can act as signals that affect, for example, neural stem cells (NSCs) residing in niches of the ventricular wall. We studied EV‐born CSF signals in an in vitro culture system. We purified EVs from the secretome of a choroid plexus cell line (Z310 cells), and from primary choroid plexus cultures and co‐cultured those EVs with NSCs isolated from the niche of the lateral and the third ventricle. EVs(Z310) and EVs(CHP) were purified by differential centrifugation. This yielded fractions of EVs of 50–150‐nm diameter that induced a complex multicellular network formation and NSC differentiation. Both types of EV converted the round NSCs to cells that extended long processes that contacted nearby, alike‐shaped cells. Mass spectrometry showed that the differentiation‐inducing EV(Z310) were enriched for membrane and membrane‐associated proteins involved in cell differentiation, membrane trafficking, and membrane organization. We hypothesize that this type of EV (Z310) cargo causes changes of stem cell morphology that leads to multicellular networks in the niches. This cell‐shape transition may represent an initial step in NSC differentiation. John Wiley and Sons Inc. 2022-11-02 2022-11 /pmc/articles/PMC9630752/ /pubmed/36325603 http://dx.doi.org/10.1002/jev2.12276 Text en © 2022 The Authors. Journal of Extracellular Vesicles published by Wiley Periodicals, LLC on behalf of the International Society for Extracellular Vesicles. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Research Articles Ditte, Zuzana Silbern, Ivan Ditte, Peter Urlaub, Henning Eichele, Gregor Extracellular vesicles derived from the choroid plexus trigger the differentiation of neural stem cells |
title | Extracellular vesicles derived from the choroid plexus trigger the differentiation of neural stem cells |
title_full | Extracellular vesicles derived from the choroid plexus trigger the differentiation of neural stem cells |
title_fullStr | Extracellular vesicles derived from the choroid plexus trigger the differentiation of neural stem cells |
title_full_unstemmed | Extracellular vesicles derived from the choroid plexus trigger the differentiation of neural stem cells |
title_short | Extracellular vesicles derived from the choroid plexus trigger the differentiation of neural stem cells |
title_sort | extracellular vesicles derived from the choroid plexus trigger the differentiation of neural stem cells |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9630752/ https://www.ncbi.nlm.nih.gov/pubmed/36325603 http://dx.doi.org/10.1002/jev2.12276 |
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