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Ankfy1 Is Involved in the Maintenance of Cerebellar Purkinje Cells

Purkinje cells are critical for the function of cerebellum. The degeneration of Purkinje cells leads to defects in motion control. We have found that Purkinje cells specifically express Ankfy1 protein during development and in adult. This protein seems to play minor functions during development as A...

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Autores principales: Chang, Liansheng, Soomro, Shahid Hussain, Zhang, Hongfeng, Fu, Hui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8008124/
https://www.ncbi.nlm.nih.gov/pubmed/33796010
http://dx.doi.org/10.3389/fncel.2021.648801
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author Chang, Liansheng
Soomro, Shahid Hussain
Zhang, Hongfeng
Fu, Hui
author_facet Chang, Liansheng
Soomro, Shahid Hussain
Zhang, Hongfeng
Fu, Hui
author_sort Chang, Liansheng
collection PubMed
description Purkinje cells are critical for the function of cerebellum. The degeneration of Purkinje cells leads to defects in motion control. We have found that Purkinje cells specifically express Ankfy1 protein during development and in adult. This protein seems to play minor functions during development as Ankfy1 knockout mice appear normal till adult. However, at 9-month-old, knockout mice showed abnormal cerebellum with reduced vermis size and developed defective motor function. Further investigation demonstrated that the cerebellum of the mutant mouse has lost most of its Purkinje cells, while other cerebellar cells remained largely normal. Our data suggested that the Ankfy1 might be important for the maintenance of cerebellar Purkinje cells.
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spelling pubmed-80081242021-03-31 Ankfy1 Is Involved in the Maintenance of Cerebellar Purkinje Cells Chang, Liansheng Soomro, Shahid Hussain Zhang, Hongfeng Fu, Hui Front Cell Neurosci Cellular Neuroscience Purkinje cells are critical for the function of cerebellum. The degeneration of Purkinje cells leads to defects in motion control. We have found that Purkinje cells specifically express Ankfy1 protein during development and in adult. This protein seems to play minor functions during development as Ankfy1 knockout mice appear normal till adult. However, at 9-month-old, knockout mice showed abnormal cerebellum with reduced vermis size and developed defective motor function. Further investigation demonstrated that the cerebellum of the mutant mouse has lost most of its Purkinje cells, while other cerebellar cells remained largely normal. Our data suggested that the Ankfy1 might be important for the maintenance of cerebellar Purkinje cells. Frontiers Media S.A. 2021-03-16 /pmc/articles/PMC8008124/ /pubmed/33796010 http://dx.doi.org/10.3389/fncel.2021.648801 Text en Copyright © 2021 Chang, Soomro, Zhang and Fu. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cellular Neuroscience
Chang, Liansheng
Soomro, Shahid Hussain
Zhang, Hongfeng
Fu, Hui
Ankfy1 Is Involved in the Maintenance of Cerebellar Purkinje Cells
title Ankfy1 Is Involved in the Maintenance of Cerebellar Purkinje Cells
title_full Ankfy1 Is Involved in the Maintenance of Cerebellar Purkinje Cells
title_fullStr Ankfy1 Is Involved in the Maintenance of Cerebellar Purkinje Cells
title_full_unstemmed Ankfy1 Is Involved in the Maintenance of Cerebellar Purkinje Cells
title_short Ankfy1 Is Involved in the Maintenance of Cerebellar Purkinje Cells
title_sort ankfy1 is involved in the maintenance of cerebellar purkinje cells
topic Cellular Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8008124/
https://www.ncbi.nlm.nih.gov/pubmed/33796010
http://dx.doi.org/10.3389/fncel.2021.648801
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