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Dendritic planarity of Purkinje cells is independent of Reelin signaling
The dendritic planarity of Purkinje cells is critical for cerebellar circuit formation. In the absence of Crk and CrkL, the Reelin pathway does not function resulting in partial Purkinje cell migration and defective dendritogenesis. However, the relationships among Purkinje cell migration, dendritic...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4481330/ https://www.ncbi.nlm.nih.gov/pubmed/24828132 http://dx.doi.org/10.1007/s00429-014-0780-2 |
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author | Kim, Jinkyung Park, Tae-Ju Kwon, Namseop Lee, Dongmyeong Kim, Seunghwan Kohmura, Yoshiki Ishikawa, Tetsuya Kim, Kyong-Tai Curran, Tom Je, Jung Ho |
author_facet | Kim, Jinkyung Park, Tae-Ju Kwon, Namseop Lee, Dongmyeong Kim, Seunghwan Kohmura, Yoshiki Ishikawa, Tetsuya Kim, Kyong-Tai Curran, Tom Je, Jung Ho |
author_sort | Kim, Jinkyung |
collection | PubMed |
description | The dendritic planarity of Purkinje cells is critical for cerebellar circuit formation. In the absence of Crk and CrkL, the Reelin pathway does not function resulting in partial Purkinje cell migration and defective dendritogenesis. However, the relationships among Purkinje cell migration, dendritic development and Reelin signaling have not been clearly delineated. Here, we use synchrotron X-ray microscopy to obtain 3-D images of Golgi-stained Purkinje cell dendrites. Purkinje cells that failed to migrate completely exhibited conical dendrites with abnormal 3-D arborization and reduced dendritic complexity. Furthermore, their spines were fewer in number with a distorted morphology. In contrast, Purkinje cells that migrated successfully displayed planar dendritic and spine morphologies similar to normal cells, despite reduced dendritic complexity. These results indicate that, during cerebellar formation, Purkinje cells migrate into an environment that supports development of dendritic planarity and spine formation. While Reelin signaling is important for the migration process, it does not make a direct major contribution to dendrite formation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00429-014-0780-2) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4481330 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-44813302015-07-02 Dendritic planarity of Purkinje cells is independent of Reelin signaling Kim, Jinkyung Park, Tae-Ju Kwon, Namseop Lee, Dongmyeong Kim, Seunghwan Kohmura, Yoshiki Ishikawa, Tetsuya Kim, Kyong-Tai Curran, Tom Je, Jung Ho Brain Struct Funct Original Article The dendritic planarity of Purkinje cells is critical for cerebellar circuit formation. In the absence of Crk and CrkL, the Reelin pathway does not function resulting in partial Purkinje cell migration and defective dendritogenesis. However, the relationships among Purkinje cell migration, dendritic development and Reelin signaling have not been clearly delineated. Here, we use synchrotron X-ray microscopy to obtain 3-D images of Golgi-stained Purkinje cell dendrites. Purkinje cells that failed to migrate completely exhibited conical dendrites with abnormal 3-D arborization and reduced dendritic complexity. Furthermore, their spines were fewer in number with a distorted morphology. In contrast, Purkinje cells that migrated successfully displayed planar dendritic and spine morphologies similar to normal cells, despite reduced dendritic complexity. These results indicate that, during cerebellar formation, Purkinje cells migrate into an environment that supports development of dendritic planarity and spine formation. While Reelin signaling is important for the migration process, it does not make a direct major contribution to dendrite formation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00429-014-0780-2) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2014-05-15 2015 /pmc/articles/PMC4481330/ /pubmed/24828132 http://dx.doi.org/10.1007/s00429-014-0780-2 Text en © The Author(s) 2014 https://creativecommons.org/licenses/by/4.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. |
spellingShingle | Original Article Kim, Jinkyung Park, Tae-Ju Kwon, Namseop Lee, Dongmyeong Kim, Seunghwan Kohmura, Yoshiki Ishikawa, Tetsuya Kim, Kyong-Tai Curran, Tom Je, Jung Ho Dendritic planarity of Purkinje cells is independent of Reelin signaling |
title | Dendritic planarity of Purkinje cells is independent of Reelin signaling |
title_full | Dendritic planarity of Purkinje cells is independent of Reelin signaling |
title_fullStr | Dendritic planarity of Purkinje cells is independent of Reelin signaling |
title_full_unstemmed | Dendritic planarity of Purkinje cells is independent of Reelin signaling |
title_short | Dendritic planarity of Purkinje cells is independent of Reelin signaling |
title_sort | dendritic planarity of purkinje cells is independent of reelin signaling |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4481330/ https://www.ncbi.nlm.nih.gov/pubmed/24828132 http://dx.doi.org/10.1007/s00429-014-0780-2 |
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