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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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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. |
format | Online Article Text |
id | pubmed-4754753 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
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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