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Increased 3-O-sulfated heparan sulfate in Alzheimer’s disease brain is associated with genetic risk gene HS3ST1
HS3ST1 is a genetic risk gene associated with Alzheimer’s disease (AD) and overexpressed in patients, but how it contributes to the disease progression is unknown. We report the analysis of brain heparan sulfate (HS) from AD and other tauopathies using a LC-MS/MS method. A specific 3-O-sulfated HS d...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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American Association for the Advancement of Science
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10219595/ https://www.ncbi.nlm.nih.gov/pubmed/37235665 http://dx.doi.org/10.1126/sciadv.adf6232 |
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author | Wang, Zhangjie Patel, Vaishali N. Song, Xuehong Xu, Yongmei Kaminski, Andrea M. Doan, Vivien Uyen Su, Guowei Liao, Yien Mah, Dylan Zhang, Fuming Pagadala, Vijayakanth Wang, Chunyu Pedersen, Lars C. Wang, Lianchun Hoffman, Matthew P. Gearing, Marla Liu, Jian |
author_facet | Wang, Zhangjie Patel, Vaishali N. Song, Xuehong Xu, Yongmei Kaminski, Andrea M. Doan, Vivien Uyen Su, Guowei Liao, Yien Mah, Dylan Zhang, Fuming Pagadala, Vijayakanth Wang, Chunyu Pedersen, Lars C. Wang, Lianchun Hoffman, Matthew P. Gearing, Marla Liu, Jian |
author_sort | Wang, Zhangjie |
collection | PubMed |
description | HS3ST1 is a genetic risk gene associated with Alzheimer’s disease (AD) and overexpressed in patients, but how it contributes to the disease progression is unknown. We report the analysis of brain heparan sulfate (HS) from AD and other tauopathies using a LC-MS/MS method. A specific 3-O-sulfated HS displayed sevenfold increase in the AD group (n = 14, P < 0.0005). Analysis of the HS modified by recombinant sulfotransferases and HS from genetic knockout mice revealed that the specific 3-O-sulfated HS is made by 3-O-sulfotransferase isoform 1 (3-OST-1), which is encoded by the HS3ST1 gene. A synthetic tetradecasaccharide (14-mer) carrying the specific 3-O-sulfated domain displayed stronger inhibition for tau internalization than a 14-mer without the domain, suggesting that the 3-O-sulfated HS is used in tau cellular uptake. Our findings suggest that the overexpression of HS3ST1 gene may enhance the spread of tau pathology, uncovering a previously unidentified therapeutic target for AD. |
format | Online Article Text |
id | pubmed-10219595 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-102195952023-05-27 Increased 3-O-sulfated heparan sulfate in Alzheimer’s disease brain is associated with genetic risk gene HS3ST1 Wang, Zhangjie Patel, Vaishali N. Song, Xuehong Xu, Yongmei Kaminski, Andrea M. Doan, Vivien Uyen Su, Guowei Liao, Yien Mah, Dylan Zhang, Fuming Pagadala, Vijayakanth Wang, Chunyu Pedersen, Lars C. Wang, Lianchun Hoffman, Matthew P. Gearing, Marla Liu, Jian Sci Adv Neuroscience HS3ST1 is a genetic risk gene associated with Alzheimer’s disease (AD) and overexpressed in patients, but how it contributes to the disease progression is unknown. We report the analysis of brain heparan sulfate (HS) from AD and other tauopathies using a LC-MS/MS method. A specific 3-O-sulfated HS displayed sevenfold increase in the AD group (n = 14, P < 0.0005). Analysis of the HS modified by recombinant sulfotransferases and HS from genetic knockout mice revealed that the specific 3-O-sulfated HS is made by 3-O-sulfotransferase isoform 1 (3-OST-1), which is encoded by the HS3ST1 gene. A synthetic tetradecasaccharide (14-mer) carrying the specific 3-O-sulfated domain displayed stronger inhibition for tau internalization than a 14-mer without the domain, suggesting that the 3-O-sulfated HS is used in tau cellular uptake. Our findings suggest that the overexpression of HS3ST1 gene may enhance the spread of tau pathology, uncovering a previously unidentified therapeutic target for AD. American Association for the Advancement of Science 2023-05-26 /pmc/articles/PMC10219595/ /pubmed/37235665 http://dx.doi.org/10.1126/sciadv.adf6232 Text en Copyright © 2023 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Neuroscience Wang, Zhangjie Patel, Vaishali N. Song, Xuehong Xu, Yongmei Kaminski, Andrea M. Doan, Vivien Uyen Su, Guowei Liao, Yien Mah, Dylan Zhang, Fuming Pagadala, Vijayakanth Wang, Chunyu Pedersen, Lars C. Wang, Lianchun Hoffman, Matthew P. Gearing, Marla Liu, Jian Increased 3-O-sulfated heparan sulfate in Alzheimer’s disease brain is associated with genetic risk gene HS3ST1 |
title | Increased 3-O-sulfated heparan sulfate in Alzheimer’s disease brain is associated with genetic risk gene HS3ST1 |
title_full | Increased 3-O-sulfated heparan sulfate in Alzheimer’s disease brain is associated with genetic risk gene HS3ST1 |
title_fullStr | Increased 3-O-sulfated heparan sulfate in Alzheimer’s disease brain is associated with genetic risk gene HS3ST1 |
title_full_unstemmed | Increased 3-O-sulfated heparan sulfate in Alzheimer’s disease brain is associated with genetic risk gene HS3ST1 |
title_short | Increased 3-O-sulfated heparan sulfate in Alzheimer’s disease brain is associated with genetic risk gene HS3ST1 |
title_sort | increased 3-o-sulfated heparan sulfate in alzheimer’s disease brain is associated with genetic risk gene hs3st1 |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10219595/ https://www.ncbi.nlm.nih.gov/pubmed/37235665 http://dx.doi.org/10.1126/sciadv.adf6232 |
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