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CTCF loss induces giant lamellar bodies in Purkinje cell dendrites

CCCTC-binding factor (CTCF) has a key role in higher-order chromatin architecture that is important for establishing and maintaining cell identity by controlling gene expression. In the mature cerebellum, CTCF is highly expressed in Purkinje cells (PCs) as compared with other cerebellar neurons. The...

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Autores principales: Hirayama, Teruyoshi, Kadooka, Yuuki, Tarusawa, Etsuko, Saitoh, Sei, Nakayama, Hisako, Hoshino, Natsumi, Nakama, Soichiro, Fukuishi, Takahiro, Kawanishi, Yudai, Umeshima, Hiroki, Tomita, Koichi, Yoshimura, Yumiko, Galjart, Niels, Hashimoto, Kouichi, Ohno, Nobuhiko, Yagi, Takeshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9706876/
https://www.ncbi.nlm.nih.gov/pubmed/36447271
http://dx.doi.org/10.1186/s40478-022-01478-6
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author Hirayama, Teruyoshi
Kadooka, Yuuki
Tarusawa, Etsuko
Saitoh, Sei
Nakayama, Hisako
Hoshino, Natsumi
Nakama, Soichiro
Fukuishi, Takahiro
Kawanishi, Yudai
Umeshima, Hiroki
Tomita, Koichi
Yoshimura, Yumiko
Galjart, Niels
Hashimoto, Kouichi
Ohno, Nobuhiko
Yagi, Takeshi
author_facet Hirayama, Teruyoshi
Kadooka, Yuuki
Tarusawa, Etsuko
Saitoh, Sei
Nakayama, Hisako
Hoshino, Natsumi
Nakama, Soichiro
Fukuishi, Takahiro
Kawanishi, Yudai
Umeshima, Hiroki
Tomita, Koichi
Yoshimura, Yumiko
Galjart, Niels
Hashimoto, Kouichi
Ohno, Nobuhiko
Yagi, Takeshi
author_sort Hirayama, Teruyoshi
collection PubMed
description CCCTC-binding factor (CTCF) has a key role in higher-order chromatin architecture that is important for establishing and maintaining cell identity by controlling gene expression. In the mature cerebellum, CTCF is highly expressed in Purkinje cells (PCs) as compared with other cerebellar neurons. The cerebellum plays an important role in motor function by regulating PCs, which are the sole output neurons, and defects in PCs cause motor dysfunction. However, the role of CTCF in PCs has not yet been explored. Here we found that the absence of CTCF in mouse PCs led to progressive motor dysfunction and abnormal dendritic morphology in those cells, which included dendritic self-avoidance defects and a proximal shift in the climbing fibre innervation territory on PC dendrites. Furthermore, we found the peculiar lamellar structures known as “giant lamellar bodies” (GLBs), which have been reported in PCs of patients with Werdnig-Hoffman disease, 13q deletion syndrome, and Krabbe disease. GLBs are localized to PC dendrites and are assumed to be associated with neurodegeneration. They have been noted, however, only in case reports following autopsy, and reports of their existence have been very limited. Here we show that GLBs were reproducibly formed in PC dendrites of a mouse model in which CTCF was deleted. GLBs were not noted in PC dendrites at infancy but instead developed over time. In conjunction with GLB development in PC dendrites, the endoplasmic reticulum was almost absent around the nuclei, the mitochondria were markedly swollen and their cristae had decreased drastically, and almost all PCs eventually disappeared as severe motor deficits manifested. Our results revealed the important role of CTCF during normal development and in maintaining PCs and provide new insights into the molecular mechanism of GLB formation during neurodegenerative disease. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40478-022-01478-6.
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spelling pubmed-97068762022-11-30 CTCF loss induces giant lamellar bodies in Purkinje cell dendrites Hirayama, Teruyoshi Kadooka, Yuuki Tarusawa, Etsuko Saitoh, Sei Nakayama, Hisako Hoshino, Natsumi Nakama, Soichiro Fukuishi, Takahiro Kawanishi, Yudai Umeshima, Hiroki Tomita, Koichi Yoshimura, Yumiko Galjart, Niels Hashimoto, Kouichi Ohno, Nobuhiko Yagi, Takeshi Acta Neuropathol Commun Research CCCTC-binding factor (CTCF) has a key role in higher-order chromatin architecture that is important for establishing and maintaining cell identity by controlling gene expression. In the mature cerebellum, CTCF is highly expressed in Purkinje cells (PCs) as compared with other cerebellar neurons. The cerebellum plays an important role in motor function by regulating PCs, which are the sole output neurons, and defects in PCs cause motor dysfunction. However, the role of CTCF in PCs has not yet been explored. Here we found that the absence of CTCF in mouse PCs led to progressive motor dysfunction and abnormal dendritic morphology in those cells, which included dendritic self-avoidance defects and a proximal shift in the climbing fibre innervation territory on PC dendrites. Furthermore, we found the peculiar lamellar structures known as “giant lamellar bodies” (GLBs), which have been reported in PCs of patients with Werdnig-Hoffman disease, 13q deletion syndrome, and Krabbe disease. GLBs are localized to PC dendrites and are assumed to be associated with neurodegeneration. They have been noted, however, only in case reports following autopsy, and reports of their existence have been very limited. Here we show that GLBs were reproducibly formed in PC dendrites of a mouse model in which CTCF was deleted. GLBs were not noted in PC dendrites at infancy but instead developed over time. In conjunction with GLB development in PC dendrites, the endoplasmic reticulum was almost absent around the nuclei, the mitochondria were markedly swollen and their cristae had decreased drastically, and almost all PCs eventually disappeared as severe motor deficits manifested. Our results revealed the important role of CTCF during normal development and in maintaining PCs and provide new insights into the molecular mechanism of GLB formation during neurodegenerative disease. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40478-022-01478-6. BioMed Central 2022-11-29 /pmc/articles/PMC9706876/ /pubmed/36447271 http://dx.doi.org/10.1186/s40478-022-01478-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Hirayama, Teruyoshi
Kadooka, Yuuki
Tarusawa, Etsuko
Saitoh, Sei
Nakayama, Hisako
Hoshino, Natsumi
Nakama, Soichiro
Fukuishi, Takahiro
Kawanishi, Yudai
Umeshima, Hiroki
Tomita, Koichi
Yoshimura, Yumiko
Galjart, Niels
Hashimoto, Kouichi
Ohno, Nobuhiko
Yagi, Takeshi
CTCF loss induces giant lamellar bodies in Purkinje cell dendrites
title CTCF loss induces giant lamellar bodies in Purkinje cell dendrites
title_full CTCF loss induces giant lamellar bodies in Purkinje cell dendrites
title_fullStr CTCF loss induces giant lamellar bodies in Purkinje cell dendrites
title_full_unstemmed CTCF loss induces giant lamellar bodies in Purkinje cell dendrites
title_short CTCF loss induces giant lamellar bodies in Purkinje cell dendrites
title_sort ctcf loss induces giant lamellar bodies in purkinje cell dendrites
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9706876/
https://www.ncbi.nlm.nih.gov/pubmed/36447271
http://dx.doi.org/10.1186/s40478-022-01478-6
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