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Eml1 loss impairs apical progenitor spindle length and soma shape in the developing cerebral cortex

The ventricular zone (VZ) of the developing cerebral cortex is a pseudostratified epithelium that contains progenitors undergoing precisely regulated divisions at its most apical side, the ventricular lining (VL). Mitotic perturbations can contribute to pathological mechanisms leading to cortical ma...

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Autores principales: Bizzotto, Sara, Uzquiano, Ana, Dingli, Florent, Ershov, Dmitry, Houllier, Anne, Arras, Guillaume, Richards, Mark, Loew, Damarys, Minc, Nicolas, Croquelois, Alexandre, Houdusse, Anne, Francis, Fiona
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5725533/
https://www.ncbi.nlm.nih.gov/pubmed/29229923
http://dx.doi.org/10.1038/s41598-017-15253-4
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author Bizzotto, Sara
Uzquiano, Ana
Dingli, Florent
Ershov, Dmitry
Houllier, Anne
Arras, Guillaume
Richards, Mark
Loew, Damarys
Minc, Nicolas
Croquelois, Alexandre
Houdusse, Anne
Francis, Fiona
author_facet Bizzotto, Sara
Uzquiano, Ana
Dingli, Florent
Ershov, Dmitry
Houllier, Anne
Arras, Guillaume
Richards, Mark
Loew, Damarys
Minc, Nicolas
Croquelois, Alexandre
Houdusse, Anne
Francis, Fiona
author_sort Bizzotto, Sara
collection PubMed
description The ventricular zone (VZ) of the developing cerebral cortex is a pseudostratified epithelium that contains progenitors undergoing precisely regulated divisions at its most apical side, the ventricular lining (VL). Mitotic perturbations can contribute to pathological mechanisms leading to cortical malformations. The HeCo mutant mouse exhibits subcortical band heterotopia (SBH), likely to be initiated by progenitor delamination from the VZ early during corticogenesis. The causes for this are however, currently unknown. Eml1, a microtubule (MT)-associated protein of the EMAP family, is impaired in these mice. We first show that MT dynamics are perturbed in mutant progenitor cells in vitro. These may influence interphase and mitotic MT mechanisms and indeed, centrosome and primary cilia were altered and spindles were found to be abnormally long in HeCo progenitors. Consistently, MT and spindle length regulators were identified in EML1 pulldowns from embryonic brain extracts. Finally, we found that mitotic cell shape is also abnormal in the mutant VZ. These previously unidentified VZ characteristics suggest altered cell constraints which may contribute to cell delamination.
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spelling pubmed-57255332017-12-13 Eml1 loss impairs apical progenitor spindle length and soma shape in the developing cerebral cortex Bizzotto, Sara Uzquiano, Ana Dingli, Florent Ershov, Dmitry Houllier, Anne Arras, Guillaume Richards, Mark Loew, Damarys Minc, Nicolas Croquelois, Alexandre Houdusse, Anne Francis, Fiona Sci Rep Article The ventricular zone (VZ) of the developing cerebral cortex is a pseudostratified epithelium that contains progenitors undergoing precisely regulated divisions at its most apical side, the ventricular lining (VL). Mitotic perturbations can contribute to pathological mechanisms leading to cortical malformations. The HeCo mutant mouse exhibits subcortical band heterotopia (SBH), likely to be initiated by progenitor delamination from the VZ early during corticogenesis. The causes for this are however, currently unknown. Eml1, a microtubule (MT)-associated protein of the EMAP family, is impaired in these mice. We first show that MT dynamics are perturbed in mutant progenitor cells in vitro. These may influence interphase and mitotic MT mechanisms and indeed, centrosome and primary cilia were altered and spindles were found to be abnormally long in HeCo progenitors. Consistently, MT and spindle length regulators were identified in EML1 pulldowns from embryonic brain extracts. Finally, we found that mitotic cell shape is also abnormal in the mutant VZ. These previously unidentified VZ characteristics suggest altered cell constraints which may contribute to cell delamination. Nature Publishing Group UK 2017-12-11 /pmc/articles/PMC5725533/ /pubmed/29229923 http://dx.doi.org/10.1038/s41598-017-15253-4 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Bizzotto, Sara
Uzquiano, Ana
Dingli, Florent
Ershov, Dmitry
Houllier, Anne
Arras, Guillaume
Richards, Mark
Loew, Damarys
Minc, Nicolas
Croquelois, Alexandre
Houdusse, Anne
Francis, Fiona
Eml1 loss impairs apical progenitor spindle length and soma shape in the developing cerebral cortex
title Eml1 loss impairs apical progenitor spindle length and soma shape in the developing cerebral cortex
title_full Eml1 loss impairs apical progenitor spindle length and soma shape in the developing cerebral cortex
title_fullStr Eml1 loss impairs apical progenitor spindle length and soma shape in the developing cerebral cortex
title_full_unstemmed Eml1 loss impairs apical progenitor spindle length and soma shape in the developing cerebral cortex
title_short Eml1 loss impairs apical progenitor spindle length and soma shape in the developing cerebral cortex
title_sort eml1 loss impairs apical progenitor spindle length and soma shape in the developing cerebral cortex
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5725533/
https://www.ncbi.nlm.nih.gov/pubmed/29229923
http://dx.doi.org/10.1038/s41598-017-15253-4
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