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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...

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Autores principales: Kim, Jinkyung, Park, Tae-Ju, Kwon, Namseop, Lee, Dongmyeong, Kim, Seunghwan, Kohmura, Yoshiki, Ishikawa, Tetsuya, Kim, Kyong-Tai, Curran, Tom, Je, Jung Ho
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2014
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.
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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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