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Non-canonical features of the Golgi apparatus in bipolar epithelial neural stem cells

Apical radial glia (aRG), the stem cells in developing neocortex, are unique bipolar epithelial cells, extending an apical process to the ventricle and a basal process to the basal lamina. Here, we report novel features of the Golgi apparatus, a central organelle for cell polarity, in mouse aRGs. Th...

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Autores principales: Taverna, Elena, Mora-Bermúdez, Felipe, Strzyz, Paulina J., Florio, Marta, Icha, Jaroslav, Haffner, Christiane, Norden, Caren, Wilsch-Bräuninger, Michaela, Huttner, Wieland B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4754753/
https://www.ncbi.nlm.nih.gov/pubmed/26879757
http://dx.doi.org/10.1038/srep21206
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author Taverna, Elena
Mora-Bermúdez, Felipe
Strzyz, Paulina J.
Florio, Marta
Icha, Jaroslav
Haffner, Christiane
Norden, Caren
Wilsch-Bräuninger, Michaela
Huttner, Wieland B.
author_facet Taverna, Elena
Mora-Bermúdez, Felipe
Strzyz, Paulina J.
Florio, Marta
Icha, Jaroslav
Haffner, Christiane
Norden, Caren
Wilsch-Bräuninger, Michaela
Huttner, Wieland B.
author_sort Taverna, Elena
collection PubMed
description Apical radial glia (aRG), the stem cells in developing neocortex, are unique bipolar epithelial cells, extending an apical process to the ventricle and a basal process to the basal lamina. Here, we report novel features of the Golgi apparatus, a central organelle for cell polarity, in mouse aRGs. The Golgi was confined to the apical process but not associated with apical centrosome(s). In contrast, in aRG-derived, delaminating basal progenitors that lose apical polarity, the Golgi became pericentrosomal. The aRG Golgi underwent evolutionarily conserved, accordion-like compression and extension concomitant with cell cycle-dependent nuclear migration. Importantly, in line with endoplasmic reticulum but not Golgi being present in the aRG basal process, its plasma membrane contained glycans lacking Golgi processing, consistent with direct ER-to-cell surface membrane traffic. Our study reveals hitherto unknown complexity of neural stem cell polarity, differential Golgi contribution to their specific architecture, and fundamental Golgi re-organization upon cell fate change.
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spelling pubmed-47547532016-02-24 Non-canonical features of the Golgi apparatus in bipolar epithelial neural stem cells Taverna, Elena Mora-Bermúdez, Felipe Strzyz, Paulina J. Florio, Marta Icha, Jaroslav Haffner, Christiane Norden, Caren Wilsch-Bräuninger, Michaela Huttner, Wieland B. Sci Rep Article Apical radial glia (aRG), the stem cells in developing neocortex, are unique bipolar epithelial cells, extending an apical process to the ventricle and a basal process to the basal lamina. Here, we report novel features of the Golgi apparatus, a central organelle for cell polarity, in mouse aRGs. The Golgi was confined to the apical process but not associated with apical centrosome(s). In contrast, in aRG-derived, delaminating basal progenitors that lose apical polarity, the Golgi became pericentrosomal. The aRG Golgi underwent evolutionarily conserved, accordion-like compression and extension concomitant with cell cycle-dependent nuclear migration. Importantly, in line with endoplasmic reticulum but not Golgi being present in the aRG basal process, its plasma membrane contained glycans lacking Golgi processing, consistent with direct ER-to-cell surface membrane traffic. Our study reveals hitherto unknown complexity of neural stem cell polarity, differential Golgi contribution to their specific architecture, and fundamental Golgi re-organization upon cell fate change. Nature Publishing Group 2016-02-16 /pmc/articles/PMC4754753/ /pubmed/26879757 http://dx.doi.org/10.1038/srep21206 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ 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
Taverna, Elena
Mora-Bermúdez, Felipe
Strzyz, Paulina J.
Florio, Marta
Icha, Jaroslav
Haffner, Christiane
Norden, Caren
Wilsch-Bräuninger, Michaela
Huttner, Wieland B.
Non-canonical features of the Golgi apparatus in bipolar epithelial neural stem cells
title Non-canonical features of the Golgi apparatus in bipolar epithelial neural stem cells
title_full Non-canonical features of the Golgi apparatus in bipolar epithelial neural stem cells
title_fullStr Non-canonical features of the Golgi apparatus in bipolar epithelial neural stem cells
title_full_unstemmed Non-canonical features of the Golgi apparatus in bipolar epithelial neural stem cells
title_short Non-canonical features of the Golgi apparatus in bipolar epithelial neural stem cells
title_sort non-canonical features of the golgi apparatus in bipolar epithelial neural stem cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4754753/
https://www.ncbi.nlm.nih.gov/pubmed/26879757
http://dx.doi.org/10.1038/srep21206
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