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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2017
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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. |
format | Online Article Text |
id | pubmed-5600531 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
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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