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Syntaxins 6 and 8 facilitate tau into secretory pathways
Tau pathology initiates in defined brain regions and is known to spread along neuronal connections as symptoms progress in Alzheimer's disease (AD) and other tauopathies. This spread requires the release of tau from donor cells, but the underlying molecular mechanisms remained unknown. Here, we...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Portland Press Ltd.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8057678/ https://www.ncbi.nlm.nih.gov/pubmed/33769438 http://dx.doi.org/10.1042/BCJ20200664 |
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author | Lee, Wei Siang Tan, Daniel CS Deng, Yuanyuan vanHummel, Annika Ippati, Stefania Stevens, Claire Carmona-Mora, Paulina Ariawan, Daryl Hou, Liming Stefen, Holly Tomanic, Tamara Bi, Mian Tomasetig, Florence Martin, Adam Fath, Thomas Palmer, Stephen Ke, Yazi D. Ittner, Lars M. |
author_facet | Lee, Wei Siang Tan, Daniel CS Deng, Yuanyuan vanHummel, Annika Ippati, Stefania Stevens, Claire Carmona-Mora, Paulina Ariawan, Daryl Hou, Liming Stefen, Holly Tomanic, Tamara Bi, Mian Tomasetig, Florence Martin, Adam Fath, Thomas Palmer, Stephen Ke, Yazi D. Ittner, Lars M. |
author_sort | Lee, Wei Siang |
collection | PubMed |
description | Tau pathology initiates in defined brain regions and is known to spread along neuronal connections as symptoms progress in Alzheimer's disease (AD) and other tauopathies. This spread requires the release of tau from donor cells, but the underlying molecular mechanisms remained unknown. Here, we established the interactome of the C-terminal tail region of tau and identified syntaxin 8 (STX8) as a mediator of tau release from cells. Similarly, we showed the syntaxin 6 (STX6), part of the same SNARE family as STX8 also facilitated tau release. STX6 was previously genetically linked to progressive supranuclear palsy (PSP), a tauopathy. Finally, we demonstrated that the transmembrane domain of STX6 is required and sufficient to mediate tau secretion. The differential role of STX6 and STX8 in alternative secretory pathways suggests the association of tau with different secretory processes. Taken together, both syntaxins, STX6 and STX8, may contribute to AD and PSP pathogenesis by mediating release of tau from cells and facilitating pathology spreading. |
format | Online Article Text |
id | pubmed-8057678 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Portland Press Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-80576782021-04-29 Syntaxins 6 and 8 facilitate tau into secretory pathways Lee, Wei Siang Tan, Daniel CS Deng, Yuanyuan vanHummel, Annika Ippati, Stefania Stevens, Claire Carmona-Mora, Paulina Ariawan, Daryl Hou, Liming Stefen, Holly Tomanic, Tamara Bi, Mian Tomasetig, Florence Martin, Adam Fath, Thomas Palmer, Stephen Ke, Yazi D. Ittner, Lars M. Biochem J Aging Tau pathology initiates in defined brain regions and is known to spread along neuronal connections as symptoms progress in Alzheimer's disease (AD) and other tauopathies. This spread requires the release of tau from donor cells, but the underlying molecular mechanisms remained unknown. Here, we established the interactome of the C-terminal tail region of tau and identified syntaxin 8 (STX8) as a mediator of tau release from cells. Similarly, we showed the syntaxin 6 (STX6), part of the same SNARE family as STX8 also facilitated tau release. STX6 was previously genetically linked to progressive supranuclear palsy (PSP), a tauopathy. Finally, we demonstrated that the transmembrane domain of STX6 is required and sufficient to mediate tau secretion. The differential role of STX6 and STX8 in alternative secretory pathways suggests the association of tau with different secretory processes. Taken together, both syntaxins, STX6 and STX8, may contribute to AD and PSP pathogenesis by mediating release of tau from cells and facilitating pathology spreading. Portland Press Ltd. 2021-04-16 2021-04-16 /pmc/articles/PMC8057678/ /pubmed/33769438 http://dx.doi.org/10.1042/BCJ20200664 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . Open access for this article was enabled by the participation of Macquarie University in an all-inclusive Read & Publish pilot with Portland Press and the Biochemical Society under a transformative agreement with CAUL. |
spellingShingle | Aging Lee, Wei Siang Tan, Daniel CS Deng, Yuanyuan vanHummel, Annika Ippati, Stefania Stevens, Claire Carmona-Mora, Paulina Ariawan, Daryl Hou, Liming Stefen, Holly Tomanic, Tamara Bi, Mian Tomasetig, Florence Martin, Adam Fath, Thomas Palmer, Stephen Ke, Yazi D. Ittner, Lars M. Syntaxins 6 and 8 facilitate tau into secretory pathways |
title | Syntaxins 6 and 8 facilitate tau into secretory pathways |
title_full | Syntaxins 6 and 8 facilitate tau into secretory pathways |
title_fullStr | Syntaxins 6 and 8 facilitate tau into secretory pathways |
title_full_unstemmed | Syntaxins 6 and 8 facilitate tau into secretory pathways |
title_short | Syntaxins 6 and 8 facilitate tau into secretory pathways |
title_sort | syntaxins 6 and 8 facilitate tau into secretory pathways |
topic | Aging |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8057678/ https://www.ncbi.nlm.nih.gov/pubmed/33769438 http://dx.doi.org/10.1042/BCJ20200664 |
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