Amyloid-β42/40 ratio drives tau pathology in 3D human neural cell culture models of Alzheimer’s disease

The relationship between amyloid-β species and tau pathology in Alzheimer’s disease is not fully understood. Here, the authors show that it is the increased ratio of amyloid-β42 and 40 isoforms drives tau pathology in 3D human neural cell culture models of the disease.

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Autores principales: Sang Su Kwak, Kevin J. Washicosky, Emma Brand, Djuna von Maydell, Jenna Aronson, Susan Kim, Diane E. Capen, Murat Cetinbas, Ruslan Sadreyev, Shen Ning, Enjana Bylykbashi, Weiming Xia, Steven L. Wagner, Se Hoon Choi, Rudolph E. Tanzi, Doo Yeon Kim
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2020
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Acceso en línea:https://doaj.org/article/0c1c3533dcca447694dd527474cb0871
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spelling oai:doaj.org-article:0c1c3533dcca447694dd527474cb08712021-12-02T17:31:08ZAmyloid-β42/40 ratio drives tau pathology in 3D human neural cell culture models of Alzheimer’s disease10.1038/s41467-020-15120-32041-1723https://doaj.org/article/0c1c3533dcca447694dd527474cb08712020-03-01T00:00:00Zhttps://doi.org/10.1038/s41467-020-15120-3https://doaj.org/toc/2041-1723The relationship between amyloid-β species and tau pathology in Alzheimer’s disease is not fully understood. Here, the authors show that it is the increased ratio of amyloid-β42 and 40 isoforms drives tau pathology in 3D human neural cell culture models of the disease.Sang Su KwakKevin J. WashicoskyEmma BrandDjuna von MaydellJenna AronsonSusan KimDiane E. CapenMurat CetinbasRuslan SadreyevShen NingEnjana BylykbashiWeiming XiaSteven L. WagnerSe Hoon ChoiRudolph E. TanziDoo Yeon KimNature PortfolioarticleScienceQENNature Communications, Vol 11, Iss 1, Pp 1-14 (2020)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Sang Su Kwak
Kevin J. Washicosky
Emma Brand
Djuna von Maydell
Jenna Aronson
Susan Kim
Diane E. Capen
Murat Cetinbas
Ruslan Sadreyev
Shen Ning
Enjana Bylykbashi
Weiming Xia
Steven L. Wagner
Se Hoon Choi
Rudolph E. Tanzi
Doo Yeon Kim
Amyloid-β42/40 ratio drives tau pathology in 3D human neural cell culture models of Alzheimer’s disease
description The relationship between amyloid-β species and tau pathology in Alzheimer’s disease is not fully understood. Here, the authors show that it is the increased ratio of amyloid-β42 and 40 isoforms drives tau pathology in 3D human neural cell culture models of the disease.
format article
author Sang Su Kwak
Kevin J. Washicosky
Emma Brand
Djuna von Maydell
Jenna Aronson
Susan Kim
Diane E. Capen
Murat Cetinbas
Ruslan Sadreyev
Shen Ning
Enjana Bylykbashi
Weiming Xia
Steven L. Wagner
Se Hoon Choi
Rudolph E. Tanzi
Doo Yeon Kim
author_facet Sang Su Kwak
Kevin J. Washicosky
Emma Brand
Djuna von Maydell
Jenna Aronson
Susan Kim
Diane E. Capen
Murat Cetinbas
Ruslan Sadreyev
Shen Ning
Enjana Bylykbashi
Weiming Xia
Steven L. Wagner
Se Hoon Choi
Rudolph E. Tanzi
Doo Yeon Kim
author_sort Sang Su Kwak
title Amyloid-β42/40 ratio drives tau pathology in 3D human neural cell culture models of Alzheimer’s disease
title_short Amyloid-β42/40 ratio drives tau pathology in 3D human neural cell culture models of Alzheimer’s disease
title_full Amyloid-β42/40 ratio drives tau pathology in 3D human neural cell culture models of Alzheimer’s disease
title_fullStr Amyloid-β42/40 ratio drives tau pathology in 3D human neural cell culture models of Alzheimer’s disease
title_full_unstemmed Amyloid-β42/40 ratio drives tau pathology in 3D human neural cell culture models of Alzheimer’s disease
title_sort amyloid-β42/40 ratio drives tau pathology in 3d human neural cell culture models of alzheimer’s disease
publisher Nature Portfolio
publishDate 2020
url https://doaj.org/article/0c1c3533dcca447694dd527474cb0871
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