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Extracellular vesicles from endothelial progenitor cells promote thyroid follicle formation
Organogenesis is a complex and dynamic process requiring reciprocal communication between different cell types. In the thyroid, thyrocyte progenitors secrete the angiocrine factor, VEGFA, to recruit endothelial cells. In return, endothelial cells promote thyrocyte organisation into spherical follicu...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6022243/ https://www.ncbi.nlm.nih.gov/pubmed/29963298 http://dx.doi.org/10.1080/20013078.2018.1487250 |
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author | Degosserie, Jonathan Heymans, Charlotte Spourquet, Catherine Halbout, Mathias D’Auria, Ludovic Van Der Smissen, Patrick Vertommen, Didier Courtoy, Pierre J. Tyteca, Donatienne Pierreux, Christophe E. |
author_facet | Degosserie, Jonathan Heymans, Charlotte Spourquet, Catherine Halbout, Mathias D’Auria, Ludovic Van Der Smissen, Patrick Vertommen, Didier Courtoy, Pierre J. Tyteca, Donatienne Pierreux, Christophe E. |
author_sort | Degosserie, Jonathan |
collection | PubMed |
description | Organogenesis is a complex and dynamic process requiring reciprocal communication between different cell types. In the thyroid, thyrocyte progenitors secrete the angiocrine factor, VEGFA, to recruit endothelial cells. In return, endothelial cells promote thyrocyte organisation into spherical follicular structures, which are responsible for thyroid hormone synthesis and storage. Medium conditioned by endothelial progenitor cells (EPCs) can promote follicle formation and lumen expansion (i.e. folliculogenesis) in an ex vivo culture system of thyroid lobes. Here, we postulated that endothelial cells instruct thyrocyte progenitors by producing extracellular vesicles (EVs). We found that medium conditioned by EPCs contain EVs with exosomal characteristics and that these vesicles can be incorporated into thyrocyte progenitors. By mass spectrometry, laminin peptides were abundantly identified in the EV preparations, probably co-sedimenting with EVs. Laminin-α1 silencing in EPC abrogated the folliculogenic effect of EVs. However, density gradient separation of EVs from laminins revealed that both EV-rich and laminin-rich fractions exhibited folliculogenic activity. In conclusion, we suggest that endothelial cells can produce EVs favouring thyrocyte organisation into follicles and lumen expansion, a mechanism promoted by laminin-α1. |
format | Online Article Text |
id | pubmed-6022243 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-60222432018-06-29 Extracellular vesicles from endothelial progenitor cells promote thyroid follicle formation Degosserie, Jonathan Heymans, Charlotte Spourquet, Catherine Halbout, Mathias D’Auria, Ludovic Van Der Smissen, Patrick Vertommen, Didier Courtoy, Pierre J. Tyteca, Donatienne Pierreux, Christophe E. J Extracell Vesicles Research Article Organogenesis is a complex and dynamic process requiring reciprocal communication between different cell types. In the thyroid, thyrocyte progenitors secrete the angiocrine factor, VEGFA, to recruit endothelial cells. In return, endothelial cells promote thyrocyte organisation into spherical follicular structures, which are responsible for thyroid hormone synthesis and storage. Medium conditioned by endothelial progenitor cells (EPCs) can promote follicle formation and lumen expansion (i.e. folliculogenesis) in an ex vivo culture system of thyroid lobes. Here, we postulated that endothelial cells instruct thyrocyte progenitors by producing extracellular vesicles (EVs). We found that medium conditioned by EPCs contain EVs with exosomal characteristics and that these vesicles can be incorporated into thyrocyte progenitors. By mass spectrometry, laminin peptides were abundantly identified in the EV preparations, probably co-sedimenting with EVs. Laminin-α1 silencing in EPC abrogated the folliculogenic effect of EVs. However, density gradient separation of EVs from laminins revealed that both EV-rich and laminin-rich fractions exhibited folliculogenic activity. In conclusion, we suggest that endothelial cells can produce EVs favouring thyrocyte organisation into follicles and lumen expansion, a mechanism promoted by laminin-α1. Taylor & Francis 2018-06-28 /pmc/articles/PMC6022243/ /pubmed/29963298 http://dx.doi.org/10.1080/20013078.2018.1487250 Text en © 2018 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group on behalf of The International Society for Extracellular Vesicles. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Degosserie, Jonathan Heymans, Charlotte Spourquet, Catherine Halbout, Mathias D’Auria, Ludovic Van Der Smissen, Patrick Vertommen, Didier Courtoy, Pierre J. Tyteca, Donatienne Pierreux, Christophe E. Extracellular vesicles from endothelial progenitor cells promote thyroid follicle formation |
title | Extracellular vesicles from endothelial progenitor cells promote thyroid follicle formation |
title_full | Extracellular vesicles from endothelial progenitor cells promote thyroid follicle formation |
title_fullStr | Extracellular vesicles from endothelial progenitor cells promote thyroid follicle formation |
title_full_unstemmed | Extracellular vesicles from endothelial progenitor cells promote thyroid follicle formation |
title_short | Extracellular vesicles from endothelial progenitor cells promote thyroid follicle formation |
title_sort | extracellular vesicles from endothelial progenitor cells promote thyroid follicle formation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6022243/ https://www.ncbi.nlm.nih.gov/pubmed/29963298 http://dx.doi.org/10.1080/20013078.2018.1487250 |
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