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Association of Retromer Deficiency and Tau Pathology in Down Syndrome

Retromer deficiency is reported in Down syndrome and correlates with amyloidosis, however, its association with tau neuropathology remains unclear. Down syndrome and control brain tissues were evaluated for phosphorylated tau, tau modulators, and cathepsin‐D activity. Several kinases and phosphatase...

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Autores principales: Curtis, Mary Elizabeth, Smith, Tiffany, Yu, Daohai, Praticò, Domenico
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8940634/
https://www.ncbi.nlm.nih.gov/pubmed/35150166
http://dx.doi.org/10.1002/ana.26321
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author Curtis, Mary Elizabeth
Smith, Tiffany
Yu, Daohai
Praticò, Domenico
author_facet Curtis, Mary Elizabeth
Smith, Tiffany
Yu, Daohai
Praticò, Domenico
author_sort Curtis, Mary Elizabeth
collection PubMed
description Retromer deficiency is reported in Down syndrome and correlates with amyloidosis, however, its association with tau neuropathology remains unclear. Down syndrome and control brain tissues were evaluated for phosphorylated tau, tau modulators, and cathepsin‐D activity. Several kinases and phosphatase PP2A were unchanged, but tau phosphorylation was elevated, and cathepsin‐D activity decreased in aged patients with Down syndrome. Retromer proteins positively associated with soluble tau, whereas pathogenic tau negatively correlated with retromer proteins and cathepsin‐D activity. Retromer deficiency and consequent reduction of cathepsin‐D activity may contribute to pathogenic tau accumulation, thus, retromer represents a viable therapeutic target against tau pathology in Down syndrome. ANN NEUROL 2022;91:561–567
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spelling pubmed-89406342022-10-14 Association of Retromer Deficiency and Tau Pathology in Down Syndrome Curtis, Mary Elizabeth Smith, Tiffany Yu, Daohai Praticò, Domenico Ann Neurol Brief Communications Retromer deficiency is reported in Down syndrome and correlates with amyloidosis, however, its association with tau neuropathology remains unclear. Down syndrome and control brain tissues were evaluated for phosphorylated tau, tau modulators, and cathepsin‐D activity. Several kinases and phosphatase PP2A were unchanged, but tau phosphorylation was elevated, and cathepsin‐D activity decreased in aged patients with Down syndrome. Retromer proteins positively associated with soluble tau, whereas pathogenic tau negatively correlated with retromer proteins and cathepsin‐D activity. Retromer deficiency and consequent reduction of cathepsin‐D activity may contribute to pathogenic tau accumulation, thus, retromer represents a viable therapeutic target against tau pathology in Down syndrome. ANN NEUROL 2022;91:561–567 John Wiley & Sons, Inc. 2022-02-25 2022-04 /pmc/articles/PMC8940634/ /pubmed/35150166 http://dx.doi.org/10.1002/ana.26321 Text en © 2022 The Authors. Annals of Neurology published by Wiley Periodicals LLC on behalf of American Neurological Association. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Brief Communications
Curtis, Mary Elizabeth
Smith, Tiffany
Yu, Daohai
Praticò, Domenico
Association of Retromer Deficiency and Tau Pathology in Down Syndrome
title Association of Retromer Deficiency and Tau Pathology in Down Syndrome
title_full Association of Retromer Deficiency and Tau Pathology in Down Syndrome
title_fullStr Association of Retromer Deficiency and Tau Pathology in Down Syndrome
title_full_unstemmed Association of Retromer Deficiency and Tau Pathology in Down Syndrome
title_short Association of Retromer Deficiency and Tau Pathology in Down Syndrome
title_sort association of retromer deficiency and tau pathology in down syndrome
topic Brief Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8940634/
https://www.ncbi.nlm.nih.gov/pubmed/35150166
http://dx.doi.org/10.1002/ana.26321
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