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Arl13b-regulated activities of primary cilia are essential for the formation of the polarized radial glial scaffold
The construction of cerebral cortex begins with the formation of radial glia. Once formed, polarized radial glial cells divide either symmetrically or asymmetrically to balance appropriate production of progenitor cells and neurons. Upon birth, neurons use the processes of radial glia as scaffolding...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3866024/ https://www.ncbi.nlm.nih.gov/pubmed/23817546 http://dx.doi.org/10.1038/nn.3451 |
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author | Higginbotham, Holden Guo, Jiami Yokota, Yukako Umberger, Nicole L. Su, Chen-Ying Li, Jingjun Verma, Nisha Hirt, Joshua Caspary, Tamara Anton, E. S. |
author_facet | Higginbotham, Holden Guo, Jiami Yokota, Yukako Umberger, Nicole L. Su, Chen-Ying Li, Jingjun Verma, Nisha Hirt, Joshua Caspary, Tamara Anton, E. S. |
author_sort | Higginbotham, Holden |
collection | PubMed |
description | The construction of cerebral cortex begins with the formation of radial glia. Once formed, polarized radial glial cells divide either symmetrically or asymmetrically to balance appropriate production of progenitor cells and neurons. Upon birth, neurons use the processes of radial glia as scaffolding for oriented migration. Radial glia thus provide an instructive structural matrix to coordinate the generation and placement of distinct groups of cortical neurons in the developing cerebral cortex. Here we show that Arl13b, a cilia-specific small GTPase mutated in Joubert syndrome patients, is critical for the initial formation of the polarized radial progenitor scaffold. Through developmental stage-specific deletion of Arl13b in mouse cortical progenitors, we found that early neuroepithelial deletion of ciliary Arl13b leads to a reversal in the apical-basal polarity of radial progenitors and aberrant neuronal placement. Arl13b modulates ciliary signaling necessary for radial glial polarity. Our findings demonstrate that Arl13b signaling in primary cilia is important for the initial formation of a polarized radial glial scaffold and suggest that disruption of this process may contribute to aberrant neurodevelopment and brain abnormalities in Joubert syndrome-related ciliopathies. |
format | Online Article Text |
id | pubmed-3866024 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
record_format | MEDLINE/PubMed |
spelling | pubmed-38660242014-02-01 Arl13b-regulated activities of primary cilia are essential for the formation of the polarized radial glial scaffold Higginbotham, Holden Guo, Jiami Yokota, Yukako Umberger, Nicole L. Su, Chen-Ying Li, Jingjun Verma, Nisha Hirt, Joshua Caspary, Tamara Anton, E. S. Nat Neurosci Article The construction of cerebral cortex begins with the formation of radial glia. Once formed, polarized radial glial cells divide either symmetrically or asymmetrically to balance appropriate production of progenitor cells and neurons. Upon birth, neurons use the processes of radial glia as scaffolding for oriented migration. Radial glia thus provide an instructive structural matrix to coordinate the generation and placement of distinct groups of cortical neurons in the developing cerebral cortex. Here we show that Arl13b, a cilia-specific small GTPase mutated in Joubert syndrome patients, is critical for the initial formation of the polarized radial progenitor scaffold. Through developmental stage-specific deletion of Arl13b in mouse cortical progenitors, we found that early neuroepithelial deletion of ciliary Arl13b leads to a reversal in the apical-basal polarity of radial progenitors and aberrant neuronal placement. Arl13b modulates ciliary signaling necessary for radial glial polarity. Our findings demonstrate that Arl13b signaling in primary cilia is important for the initial formation of a polarized radial glial scaffold and suggest that disruption of this process may contribute to aberrant neurodevelopment and brain abnormalities in Joubert syndrome-related ciliopathies. 2013-06-30 2013-08 /pmc/articles/PMC3866024/ /pubmed/23817546 http://dx.doi.org/10.1038/nn.3451 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Higginbotham, Holden Guo, Jiami Yokota, Yukako Umberger, Nicole L. Su, Chen-Ying Li, Jingjun Verma, Nisha Hirt, Joshua Caspary, Tamara Anton, E. S. Arl13b-regulated activities of primary cilia are essential for the formation of the polarized radial glial scaffold |
title | Arl13b-regulated activities of primary cilia are essential for the formation of the polarized radial glial scaffold |
title_full | Arl13b-regulated activities of primary cilia are essential for the formation of the polarized radial glial scaffold |
title_fullStr | Arl13b-regulated activities of primary cilia are essential for the formation of the polarized radial glial scaffold |
title_full_unstemmed | Arl13b-regulated activities of primary cilia are essential for the formation of the polarized radial glial scaffold |
title_short | Arl13b-regulated activities of primary cilia are essential for the formation of the polarized radial glial scaffold |
title_sort | arl13b-regulated activities of primary cilia are essential for the formation of the polarized radial glial scaffold |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3866024/ https://www.ncbi.nlm.nih.gov/pubmed/23817546 http://dx.doi.org/10.1038/nn.3451 |
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