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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2021
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.
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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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