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Alzheimer's amyloid‐β and tau protein accumulation is associated with decreased expression of the LDL receptor‐associated protein in human brain tissue
INTRODUCTION: One of the major neuropathological features of Alzheimer's disease (AD) is the accumulation of amyloid‐β (Aβ) protein in the brain. Evidence suggests that the low‐density lipoprotein receptor‐associated protein (RAP) binds strongly to Aβ and enhances its cellular uptake and that d...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7375106/ https://www.ncbi.nlm.nih.gov/pubmed/32484608 http://dx.doi.org/10.1002/brb3.1672 |
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author | Shepherd, Claire E. Affleck, Andrew J. Bahar, Anita Y. Carew‐Jones, Francine Gregory, Gillian Small, David H. Halliday, Glenda M. |
author_facet | Shepherd, Claire E. Affleck, Andrew J. Bahar, Anita Y. Carew‐Jones, Francine Gregory, Gillian Small, David H. Halliday, Glenda M. |
author_sort | Shepherd, Claire E. |
collection | PubMed |
description | INTRODUCTION: One of the major neuropathological features of Alzheimer's disease (AD) is the accumulation of amyloid‐β (Aβ) protein in the brain. Evidence suggests that the low‐density lipoprotein receptor‐associated protein (RAP) binds strongly to Aβ and enhances its cellular uptake and that decreased RAP expression correlates with increased Aβ production in animal models of AD. METHODS: The current study examined whether RAP levels change in AD human brain tissue and whether they are related to the amount of AD pathology. RAP and NeuN levels were determined by Western blot, while low‐density lipoprotein receptor‐related protein 1 (LRP1), tau and Aβ levels were determined by ELISA in the temporal cortex of 17 AD and 16 control cases. RESULTS: An increase in total Aβ and insoluble and soluble tau protein was observed in AD brain tissue. In contrast, RAP levels were significantly decreased in AD brain tissue compared to controls. Correlation analysis revealed that levels of RAP correlated with both total Aβ and soluble and insoluble tau levels. Neither LRP1 nor NeuN levels were significantly altered in AD brain tissue homogenates and did not correlate with Aβ or tau protein levels. CONCLUSION: Reduction in RAP may contribute to the accumulation and aggregation of Aβ in the AD brain. |
format | Online Article Text |
id | pubmed-7375106 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-73751062020-07-22 Alzheimer's amyloid‐β and tau protein accumulation is associated with decreased expression of the LDL receptor‐associated protein in human brain tissue Shepherd, Claire E. Affleck, Andrew J. Bahar, Anita Y. Carew‐Jones, Francine Gregory, Gillian Small, David H. Halliday, Glenda M. Brain Behav Original Research INTRODUCTION: One of the major neuropathological features of Alzheimer's disease (AD) is the accumulation of amyloid‐β (Aβ) protein in the brain. Evidence suggests that the low‐density lipoprotein receptor‐associated protein (RAP) binds strongly to Aβ and enhances its cellular uptake and that decreased RAP expression correlates with increased Aβ production in animal models of AD. METHODS: The current study examined whether RAP levels change in AD human brain tissue and whether they are related to the amount of AD pathology. RAP and NeuN levels were determined by Western blot, while low‐density lipoprotein receptor‐related protein 1 (LRP1), tau and Aβ levels were determined by ELISA in the temporal cortex of 17 AD and 16 control cases. RESULTS: An increase in total Aβ and insoluble and soluble tau protein was observed in AD brain tissue. In contrast, RAP levels were significantly decreased in AD brain tissue compared to controls. Correlation analysis revealed that levels of RAP correlated with both total Aβ and soluble and insoluble tau levels. Neither LRP1 nor NeuN levels were significantly altered in AD brain tissue homogenates and did not correlate with Aβ or tau protein levels. CONCLUSION: Reduction in RAP may contribute to the accumulation and aggregation of Aβ in the AD brain. John Wiley and Sons Inc. 2020-06-02 /pmc/articles/PMC7375106/ /pubmed/32484608 http://dx.doi.org/10.1002/brb3.1672 Text en © 2020 The Authors. Brain and Behavior published by Wiley Periodicals LLC. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Shepherd, Claire E. Affleck, Andrew J. Bahar, Anita Y. Carew‐Jones, Francine Gregory, Gillian Small, David H. Halliday, Glenda M. Alzheimer's amyloid‐β and tau protein accumulation is associated with decreased expression of the LDL receptor‐associated protein in human brain tissue |
title | Alzheimer's amyloid‐β and tau protein accumulation is associated with decreased expression of the LDL receptor‐associated protein in human brain tissue |
title_full | Alzheimer's amyloid‐β and tau protein accumulation is associated with decreased expression of the LDL receptor‐associated protein in human brain tissue |
title_fullStr | Alzheimer's amyloid‐β and tau protein accumulation is associated with decreased expression of the LDL receptor‐associated protein in human brain tissue |
title_full_unstemmed | Alzheimer's amyloid‐β and tau protein accumulation is associated with decreased expression of the LDL receptor‐associated protein in human brain tissue |
title_short | Alzheimer's amyloid‐β and tau protein accumulation is associated with decreased expression of the LDL receptor‐associated protein in human brain tissue |
title_sort | alzheimer's amyloid‐β and tau protein accumulation is associated with decreased expression of the ldl receptor‐associated protein in human brain tissue |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7375106/ https://www.ncbi.nlm.nih.gov/pubmed/32484608 http://dx.doi.org/10.1002/brb3.1672 |
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