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Synaptic and metabolic gene expression alterations in neurons that are recipients of proteopathic tau seeds
Recent studies suggest that misfolded tau molecules can be released, and taken up by adjacent neurons, propagating proteopathic seeds across neural systems. Yet critical to understanding whether tau propagation is relevant in pathophysiology of disease would be to learn if it alters neuronal propert...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7574323/ https://www.ncbi.nlm.nih.gov/pubmed/33076986 http://dx.doi.org/10.1186/s40478-020-01049-7 |
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author | Perez-Rando, Marta Dujardin, Simon Bennett, Rachel E. Commins, Caitlin Nibhanupudy, Tara Hyman, Bradley T. |
author_facet | Perez-Rando, Marta Dujardin, Simon Bennett, Rachel E. Commins, Caitlin Nibhanupudy, Tara Hyman, Bradley T. |
author_sort | Perez-Rando, Marta |
collection | PubMed |
description | Recent studies suggest that misfolded tau molecules can be released, and taken up by adjacent neurons, propagating proteopathic seeds across neural systems. Yet critical to understanding whether tau propagation is relevant in pathophysiology of disease would be to learn if it alters neuronal properties. We utilized high resolution multi-color in situ hybridization technology, RNAScope, in a well-established tau transgenic animal, and found that a subset of neurons in the cortex do not appear to express the transgene, but do develop phospho-tau positive inclusions, consistent with having received tau seeds. Recipient neurons show decreases in their expression of synaptophysin, CAMKIIα, and mouse tau in both young and old animals. These results contrast with neurons that develop tau aggregates and also overexpress the transgene, which have few changes in expression of metabolic and synaptic markers. Taken together, these results strongly suggest that tau propagation impacts neuronal functional integrity. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40478-020-01049-7) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-7574323 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-75743232020-10-20 Synaptic and metabolic gene expression alterations in neurons that are recipients of proteopathic tau seeds Perez-Rando, Marta Dujardin, Simon Bennett, Rachel E. Commins, Caitlin Nibhanupudy, Tara Hyman, Bradley T. Acta Neuropathol Commun Research Recent studies suggest that misfolded tau molecules can be released, and taken up by adjacent neurons, propagating proteopathic seeds across neural systems. Yet critical to understanding whether tau propagation is relevant in pathophysiology of disease would be to learn if it alters neuronal properties. We utilized high resolution multi-color in situ hybridization technology, RNAScope, in a well-established tau transgenic animal, and found that a subset of neurons in the cortex do not appear to express the transgene, but do develop phospho-tau positive inclusions, consistent with having received tau seeds. Recipient neurons show decreases in their expression of synaptophysin, CAMKIIα, and mouse tau in both young and old animals. These results contrast with neurons that develop tau aggregates and also overexpress the transgene, which have few changes in expression of metabolic and synaptic markers. Taken together, these results strongly suggest that tau propagation impacts neuronal functional integrity. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40478-020-01049-7) contains supplementary material, which is available to authorized users. BioMed Central 2020-10-19 /pmc/articles/PMC7574323/ /pubmed/33076986 http://dx.doi.org/10.1186/s40478-020-01049-7 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 | Research Perez-Rando, Marta Dujardin, Simon Bennett, Rachel E. Commins, Caitlin Nibhanupudy, Tara Hyman, Bradley T. Synaptic and metabolic gene expression alterations in neurons that are recipients of proteopathic tau seeds |
title | Synaptic and metabolic gene expression alterations in neurons that are recipients of proteopathic tau seeds |
title_full | Synaptic and metabolic gene expression alterations in neurons that are recipients of proteopathic tau seeds |
title_fullStr | Synaptic and metabolic gene expression alterations in neurons that are recipients of proteopathic tau seeds |
title_full_unstemmed | Synaptic and metabolic gene expression alterations in neurons that are recipients of proteopathic tau seeds |
title_short | Synaptic and metabolic gene expression alterations in neurons that are recipients of proteopathic tau seeds |
title_sort | synaptic and metabolic gene expression alterations in neurons that are recipients of proteopathic tau seeds |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7574323/ https://www.ncbi.nlm.nih.gov/pubmed/33076986 http://dx.doi.org/10.1186/s40478-020-01049-7 |
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