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Microvesicles from cerebrospinal fluid of patients with Alzheimer’s disease display reduced concentrations of tau and APP protein

Microvesicles are small membranous particles generated during cellular activation or stress. The analysis of the content and the surface of microvesicles allow conclusions about the cells they are originating from and the underlying pathology. Therefore, CSF microvesicles have been suggested to be p...

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Autores principales: Spitzer, Philipp, Mulzer, Linda-Marie, Oberstein, Timo Jan, Munoz, Luis Enrique, Lewczuk, Piotr, Kornhuber, Johannes, Herrmann, Martin, Maler, Juan Manuel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6506501/
https://www.ncbi.nlm.nih.gov/pubmed/31068645
http://dx.doi.org/10.1038/s41598-019-43607-7
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author Spitzer, Philipp
Mulzer, Linda-Marie
Oberstein, Timo Jan
Munoz, Luis Enrique
Lewczuk, Piotr
Kornhuber, Johannes
Herrmann, Martin
Maler, Juan Manuel
author_facet Spitzer, Philipp
Mulzer, Linda-Marie
Oberstein, Timo Jan
Munoz, Luis Enrique
Lewczuk, Piotr
Kornhuber, Johannes
Herrmann, Martin
Maler, Juan Manuel
author_sort Spitzer, Philipp
collection PubMed
description Microvesicles are small membranous particles generated during cellular activation or stress. The analysis of the content and the surface of microvesicles allow conclusions about the cells they are originating from and the underlying pathology. Therefore, CSF microvesicles have been suggested to be promising targets to monitor the (etio)pathology of neurodegenerative diseases. Microvesicles in the CSF of 15 patients with Alzheimer’s disease and 15 controls were analyzed by flow cytometry regarding the levels of CD3, CD4, CD45, CD64, BACE1, Aβ, APP and tau. The results were replicated in a second cohort comprising 14 patients with Alzheimer’s disease and 9 controls. The levels of tau and APP were reduced in microvesicles of Alzheimer’s disease patients. A significant change was neither observed in the number of microvesicles nor in the expression of the other antigens. Tau and APP in microvesicles separated patients with Alzheimer’s disease from controls with an AUC of 0.84 and 0.89 respectively. We conclude that tau and APP in CSF microvesicles are promising biomarkers which could directly provide information about the Alzheimer pathology on a cellular level.
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spelling pubmed-65065012019-05-21 Microvesicles from cerebrospinal fluid of patients with Alzheimer’s disease display reduced concentrations of tau and APP protein Spitzer, Philipp Mulzer, Linda-Marie Oberstein, Timo Jan Munoz, Luis Enrique Lewczuk, Piotr Kornhuber, Johannes Herrmann, Martin Maler, Juan Manuel Sci Rep Article Microvesicles are small membranous particles generated during cellular activation or stress. The analysis of the content and the surface of microvesicles allow conclusions about the cells they are originating from and the underlying pathology. Therefore, CSF microvesicles have been suggested to be promising targets to monitor the (etio)pathology of neurodegenerative diseases. Microvesicles in the CSF of 15 patients with Alzheimer’s disease and 15 controls were analyzed by flow cytometry regarding the levels of CD3, CD4, CD45, CD64, BACE1, Aβ, APP and tau. The results were replicated in a second cohort comprising 14 patients with Alzheimer’s disease and 9 controls. The levels of tau and APP were reduced in microvesicles of Alzheimer’s disease patients. A significant change was neither observed in the number of microvesicles nor in the expression of the other antigens. Tau and APP in microvesicles separated patients with Alzheimer’s disease from controls with an AUC of 0.84 and 0.89 respectively. We conclude that tau and APP in CSF microvesicles are promising biomarkers which could directly provide information about the Alzheimer pathology on a cellular level. Nature Publishing Group UK 2019-05-08 /pmc/articles/PMC6506501/ /pubmed/31068645 http://dx.doi.org/10.1038/s41598-019-43607-7 Text en © The Author(s) 2019 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Spitzer, Philipp
Mulzer, Linda-Marie
Oberstein, Timo Jan
Munoz, Luis Enrique
Lewczuk, Piotr
Kornhuber, Johannes
Herrmann, Martin
Maler, Juan Manuel
Microvesicles from cerebrospinal fluid of patients with Alzheimer’s disease display reduced concentrations of tau and APP protein
title Microvesicles from cerebrospinal fluid of patients with Alzheimer’s disease display reduced concentrations of tau and APP protein
title_full Microvesicles from cerebrospinal fluid of patients with Alzheimer’s disease display reduced concentrations of tau and APP protein
title_fullStr Microvesicles from cerebrospinal fluid of patients with Alzheimer’s disease display reduced concentrations of tau and APP protein
title_full_unstemmed Microvesicles from cerebrospinal fluid of patients with Alzheimer’s disease display reduced concentrations of tau and APP protein
title_short Microvesicles from cerebrospinal fluid of patients with Alzheimer’s disease display reduced concentrations of tau and APP protein
title_sort microvesicles from cerebrospinal fluid of patients with alzheimer’s disease display reduced concentrations of tau and app protein
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6506501/
https://www.ncbi.nlm.nih.gov/pubmed/31068645
http://dx.doi.org/10.1038/s41598-019-43607-7
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