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Tunneling nanotube (TNT)-mediated neuron-to neuron transfer of pathological Tau protein assemblies
A given cell makes exchanges with its neighbors through a variety of means ranging from diffusible factors to vesicles. Cells use also tunneling nanotubes (TNTs), filamentous-actin-containing membranous structures that bridge and connect cells. First described in immune cells, TNTs facilitate HIV-1...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5096005/ https://www.ncbi.nlm.nih.gov/pubmed/27809932 http://dx.doi.org/10.1186/s40478-016-0386-4 |
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author | Tardivel, Meryem Bégard, Séverine Bousset, Luc Dujardin, Simon Coens, Audrey Melki, Ronald Buée, Luc Colin, Morvane |
author_facet | Tardivel, Meryem Bégard, Séverine Bousset, Luc Dujardin, Simon Coens, Audrey Melki, Ronald Buée, Luc Colin, Morvane |
author_sort | Tardivel, Meryem |
collection | PubMed |
description | A given cell makes exchanges with its neighbors through a variety of means ranging from diffusible factors to vesicles. Cells use also tunneling nanotubes (TNTs), filamentous-actin-containing membranous structures that bridge and connect cells. First described in immune cells, TNTs facilitate HIV-1 transfer and are found in various cell types, including neurons. We show that the microtubule-associated protein Tau, a key player in Alzheimer’s disease, is a bona fide constituent of TNTs. This is important because Tau appears beside filamentous actin and myosin 10 as a specific marker of these fine protrusions of membranes and cytosol that are difficult to visualize. Furthermore, we observed that exogenous Tau species increase the number of TNTs established between primary neurons, thereby facilitating the intercellular transfer of Tau fibrils. In conclusion, Tau may contribute to the formation and function of the highly dynamic TNTs that may be involved in the prion-like propagation of Tau assemblies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40478-016-0386-4) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5096005 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-50960052016-11-07 Tunneling nanotube (TNT)-mediated neuron-to neuron transfer of pathological Tau protein assemblies Tardivel, Meryem Bégard, Séverine Bousset, Luc Dujardin, Simon Coens, Audrey Melki, Ronald Buée, Luc Colin, Morvane Acta Neuropathol Commun Research A given cell makes exchanges with its neighbors through a variety of means ranging from diffusible factors to vesicles. Cells use also tunneling nanotubes (TNTs), filamentous-actin-containing membranous structures that bridge and connect cells. First described in immune cells, TNTs facilitate HIV-1 transfer and are found in various cell types, including neurons. We show that the microtubule-associated protein Tau, a key player in Alzheimer’s disease, is a bona fide constituent of TNTs. This is important because Tau appears beside filamentous actin and myosin 10 as a specific marker of these fine protrusions of membranes and cytosol that are difficult to visualize. Furthermore, we observed that exogenous Tau species increase the number of TNTs established between primary neurons, thereby facilitating the intercellular transfer of Tau fibrils. In conclusion, Tau may contribute to the formation and function of the highly dynamic TNTs that may be involved in the prion-like propagation of Tau assemblies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40478-016-0386-4) contains supplementary material, which is available to authorized users. BioMed Central 2016-11-04 /pmc/articles/PMC5096005/ /pubmed/27809932 http://dx.doi.org/10.1186/s40478-016-0386-4 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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. |
spellingShingle | Research Tardivel, Meryem Bégard, Séverine Bousset, Luc Dujardin, Simon Coens, Audrey Melki, Ronald Buée, Luc Colin, Morvane Tunneling nanotube (TNT)-mediated neuron-to neuron transfer of pathological Tau protein assemblies |
title | Tunneling nanotube (TNT)-mediated neuron-to neuron transfer of pathological Tau protein assemblies |
title_full | Tunneling nanotube (TNT)-mediated neuron-to neuron transfer of pathological Tau protein assemblies |
title_fullStr | Tunneling nanotube (TNT)-mediated neuron-to neuron transfer of pathological Tau protein assemblies |
title_full_unstemmed | Tunneling nanotube (TNT)-mediated neuron-to neuron transfer of pathological Tau protein assemblies |
title_short | Tunneling nanotube (TNT)-mediated neuron-to neuron transfer of pathological Tau protein assemblies |
title_sort | tunneling nanotube (tnt)-mediated neuron-to neuron transfer of pathological tau protein assemblies |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5096005/ https://www.ncbi.nlm.nih.gov/pubmed/27809932 http://dx.doi.org/10.1186/s40478-016-0386-4 |
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