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Interplay between protein glycosylation pathways in Alzheimer’s disease

Deviations from the normal nucleoplasmic protein O-GlcNAcylation, as well as from normal protein sialylation and N-glycosylation in the secretory pathway, have been reported in Alzheimer’s disease (AD). However, the interplay between the cytoplasmic protein O-GlcNAcylation and the secretory N-/O-gly...

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Autores principales: Frenkel-Pinter, Moran, Shmueli, Merav Daniel, Raz, Chen, Yanku, Michaela, Zilberzwige, Shai, Gazit, Ehud, Segal, Daniel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5600531/
https://www.ncbi.nlm.nih.gov/pubmed/28929132
http://dx.doi.org/10.1126/sciadv.1601576
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author Frenkel-Pinter, Moran
Shmueli, Merav Daniel
Raz, Chen
Yanku, Michaela
Zilberzwige, Shai
Gazit, Ehud
Segal, Daniel
author_facet Frenkel-Pinter, Moran
Shmueli, Merav Daniel
Raz, Chen
Yanku, Michaela
Zilberzwige, Shai
Gazit, Ehud
Segal, Daniel
author_sort Frenkel-Pinter, Moran
collection PubMed
description Deviations from the normal nucleoplasmic protein O-GlcNAcylation, as well as from normal protein sialylation and N-glycosylation in the secretory pathway, have been reported in Alzheimer’s disease (AD). However, the interplay between the cytoplasmic protein O-GlcNAcylation and the secretory N-/O-glycosylation in AD has not been described. We present a comprehensive analysis of the N-, O-, and O-GlcNAc–glycomes in AD-affected brain regions as well as in AD patient serum. We detected marked differences in levels of glycan involved in both protein O-GlcNAcylation and N-/O-glycosylation between patients and healthy individuals and revealed brain region–specific glycosylation-related pathology in patients. These alterations are not general for other neurodegenerative conditions, such as frontotemporal dementia and corticobasal degeneration. The alterations in the AD glycome in the serum could potentially lead to novel glyco-based biomarkers for AD progression. Strikingly, negative interrelationship was found between the pathways of protein O-GlcNAcylation and N-/O-glycosylation, suggesting a novel intracellular cross-talk.
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spelling pubmed-56005312017-09-19 Interplay between protein glycosylation pathways in Alzheimer’s disease Frenkel-Pinter, Moran Shmueli, Merav Daniel Raz, Chen Yanku, Michaela Zilberzwige, Shai Gazit, Ehud Segal, Daniel Sci Adv Research Articles Deviations from the normal nucleoplasmic protein O-GlcNAcylation, as well as from normal protein sialylation and N-glycosylation in the secretory pathway, have been reported in Alzheimer’s disease (AD). However, the interplay between the cytoplasmic protein O-GlcNAcylation and the secretory N-/O-glycosylation in AD has not been described. We present a comprehensive analysis of the N-, O-, and O-GlcNAc–glycomes in AD-affected brain regions as well as in AD patient serum. We detected marked differences in levels of glycan involved in both protein O-GlcNAcylation and N-/O-glycosylation between patients and healthy individuals and revealed brain region–specific glycosylation-related pathology in patients. These alterations are not general for other neurodegenerative conditions, such as frontotemporal dementia and corticobasal degeneration. The alterations in the AD glycome in the serum could potentially lead to novel glyco-based biomarkers for AD progression. Strikingly, negative interrelationship was found between the pathways of protein O-GlcNAcylation and N-/O-glycosylation, suggesting a novel intracellular cross-talk. American Association for the Advancement of Science 2017-09-15 /pmc/articles/PMC5600531/ /pubmed/28929132 http://dx.doi.org/10.1126/sciadv.1601576 Text en Copyright © 2017 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). http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (http://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 Research Articles
Frenkel-Pinter, Moran
Shmueli, Merav Daniel
Raz, Chen
Yanku, Michaela
Zilberzwige, Shai
Gazit, Ehud
Segal, Daniel
Interplay between protein glycosylation pathways in Alzheimer’s disease
title Interplay between protein glycosylation pathways in Alzheimer’s disease
title_full Interplay between protein glycosylation pathways in Alzheimer’s disease
title_fullStr Interplay between protein glycosylation pathways in Alzheimer’s disease
title_full_unstemmed Interplay between protein glycosylation pathways in Alzheimer’s disease
title_short Interplay between protein glycosylation pathways in Alzheimer’s disease
title_sort interplay between protein glycosylation pathways in alzheimer’s disease
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5600531/
https://www.ncbi.nlm.nih.gov/pubmed/28929132
http://dx.doi.org/10.1126/sciadv.1601576
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