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Untangling the origin and function of granulovacuolar degeneration bodies in neurodegenerative proteinopathies

In the brains of tauopathy patients, tau pathology coincides with the presence of granulovacuolar degeneration bodies (GVBs) both at the regional and cellular level. Recently, it was shown that intracellular tau pathology causes GVB formation in experimental models thus explaining the strong correla...

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Autores principales: Wiersma, Vera I., Hoozemans, Jeroen J. M., Scheper, Wiep
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7469111/
https://www.ncbi.nlm.nih.gov/pubmed/32883341
http://dx.doi.org/10.1186/s40478-020-00996-5
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author Wiersma, Vera I.
Hoozemans, Jeroen J. M.
Scheper, Wiep
author_facet Wiersma, Vera I.
Hoozemans, Jeroen J. M.
Scheper, Wiep
author_sort Wiersma, Vera I.
collection PubMed
description In the brains of tauopathy patients, tau pathology coincides with the presence of granulovacuolar degeneration bodies (GVBs) both at the regional and cellular level. Recently, it was shown that intracellular tau pathology causes GVB formation in experimental models thus explaining the strong correlation between these neuropathological hallmarks in the human brain. These novel models of GVB formation provide opportunities for future research into GVB biology, but also urge reevaluation of previous post-mortem observations. Here, we review neuropathological data on GVBs in tauopathies and other neurodegenerative proteinopathies. We discuss the possibility that intracellular aggregates composed of proteins other than tau are also able to induce GVB formation. Furthermore, the potential mechanisms of GVB formation and the downstream functional implications hereof are outlined in view of the current available data. In addition, we provide guidelines for the identification of GVBs in tissue and cell models that will help to facilitate and streamline research towards the elucidation of the role of these enigmatic and understudied structures in neurodegeneration.
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spelling pubmed-74691112020-09-03 Untangling the origin and function of granulovacuolar degeneration bodies in neurodegenerative proteinopathies Wiersma, Vera I. Hoozemans, Jeroen J. M. Scheper, Wiep Acta Neuropathol Commun Review In the brains of tauopathy patients, tau pathology coincides with the presence of granulovacuolar degeneration bodies (GVBs) both at the regional and cellular level. Recently, it was shown that intracellular tau pathology causes GVB formation in experimental models thus explaining the strong correlation between these neuropathological hallmarks in the human brain. These novel models of GVB formation provide opportunities for future research into GVB biology, but also urge reevaluation of previous post-mortem observations. Here, we review neuropathological data on GVBs in tauopathies and other neurodegenerative proteinopathies. We discuss the possibility that intracellular aggregates composed of proteins other than tau are also able to induce GVB formation. Furthermore, the potential mechanisms of GVB formation and the downstream functional implications hereof are outlined in view of the current available data. In addition, we provide guidelines for the identification of GVBs in tissue and cell models that will help to facilitate and streamline research towards the elucidation of the role of these enigmatic and understudied structures in neurodegeneration. BioMed Central 2020-09-03 /pmc/articles/PMC7469111/ /pubmed/32883341 http://dx.doi.org/10.1186/s40478-020-00996-5 Text en © The Author(s) 2020 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/. The Creative Commons Public Domain Dedication waiver (http://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 Review
Wiersma, Vera I.
Hoozemans, Jeroen J. M.
Scheper, Wiep
Untangling the origin and function of granulovacuolar degeneration bodies in neurodegenerative proteinopathies
title Untangling the origin and function of granulovacuolar degeneration bodies in neurodegenerative proteinopathies
title_full Untangling the origin and function of granulovacuolar degeneration bodies in neurodegenerative proteinopathies
title_fullStr Untangling the origin and function of granulovacuolar degeneration bodies in neurodegenerative proteinopathies
title_full_unstemmed Untangling the origin and function of granulovacuolar degeneration bodies in neurodegenerative proteinopathies
title_short Untangling the origin and function of granulovacuolar degeneration bodies in neurodegenerative proteinopathies
title_sort untangling the origin and function of granulovacuolar degeneration bodies in neurodegenerative proteinopathies
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7469111/
https://www.ncbi.nlm.nih.gov/pubmed/32883341
http://dx.doi.org/10.1186/s40478-020-00996-5
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