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Preserved neurogenesis in non-demented individuals with AD neuropathology

Rare individuals remain cognitively intact despite the presence of neuropathology usually associated with fully symptomatic Alzheimer’s disease (AD), which we refer to as Non-Demented with Alzheimer’s disease Neuropathology (NDAN). Understanding the involved mechanism(s) of their cognitive resistanc...

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Autores principales: Briley, David, Ghirardi, Valeria, Woltjer, Randy, Renck, Alicia, Zolochevska, Olga, Taglialatela, Giulio, Micci, Maria-Adelaide
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4906289/
https://www.ncbi.nlm.nih.gov/pubmed/27298190
http://dx.doi.org/10.1038/srep27812
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author Briley, David
Ghirardi, Valeria
Woltjer, Randy
Renck, Alicia
Zolochevska, Olga
Taglialatela, Giulio
Micci, Maria-Adelaide
author_facet Briley, David
Ghirardi, Valeria
Woltjer, Randy
Renck, Alicia
Zolochevska, Olga
Taglialatela, Giulio
Micci, Maria-Adelaide
author_sort Briley, David
collection PubMed
description Rare individuals remain cognitively intact despite the presence of neuropathology usually associated with fully symptomatic Alzheimer’s disease (AD), which we refer to as Non-Demented with Alzheimer’s disease Neuropathology (NDAN). Understanding the involved mechanism(s) of their cognitive resistance may reveal novel strategies to treat AD-related dementia. In the pursuit of this goal, we determined the number of hippocampal neural stem cells (NSCs) and investigated the expression of several miRNAs in NDAN and AD subjects. Laser-capture microdissection of autopsy human hippocampus DG and qRT-PCR miRNA analyses were combined with immunofluorescence in this study. The number of SOX2(+) NSCs in the DG was significantly increased in NDAN individuals as compared to AD subjects. Further, the prevalence of SOX2(+) NSCs was found to correlate with cognitive capacity. Neurogenesis-regulating miRNAs were decreased in NDAN individuals as compared to AD patients. An increased number of NSCs and new neurons in NDAN individuals is associated with a unique expression of regulating miRNAs and strongly support a role of neurogenesis in mediating, in part, the ability of these individuals to resist the pathological burden of AD.
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spelling pubmed-49062892016-06-14 Preserved neurogenesis in non-demented individuals with AD neuropathology Briley, David Ghirardi, Valeria Woltjer, Randy Renck, Alicia Zolochevska, Olga Taglialatela, Giulio Micci, Maria-Adelaide Sci Rep Article Rare individuals remain cognitively intact despite the presence of neuropathology usually associated with fully symptomatic Alzheimer’s disease (AD), which we refer to as Non-Demented with Alzheimer’s disease Neuropathology (NDAN). Understanding the involved mechanism(s) of their cognitive resistance may reveal novel strategies to treat AD-related dementia. In the pursuit of this goal, we determined the number of hippocampal neural stem cells (NSCs) and investigated the expression of several miRNAs in NDAN and AD subjects. Laser-capture microdissection of autopsy human hippocampus DG and qRT-PCR miRNA analyses were combined with immunofluorescence in this study. The number of SOX2(+) NSCs in the DG was significantly increased in NDAN individuals as compared to AD subjects. Further, the prevalence of SOX2(+) NSCs was found to correlate with cognitive capacity. Neurogenesis-regulating miRNAs were decreased in NDAN individuals as compared to AD patients. An increased number of NSCs and new neurons in NDAN individuals is associated with a unique expression of regulating miRNAs and strongly support a role of neurogenesis in mediating, in part, the ability of these individuals to resist the pathological burden of AD. Nature Publishing Group 2016-06-14 /pmc/articles/PMC4906289/ /pubmed/27298190 http://dx.doi.org/10.1038/srep27812 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Briley, David
Ghirardi, Valeria
Woltjer, Randy
Renck, Alicia
Zolochevska, Olga
Taglialatela, Giulio
Micci, Maria-Adelaide
Preserved neurogenesis in non-demented individuals with AD neuropathology
title Preserved neurogenesis in non-demented individuals with AD neuropathology
title_full Preserved neurogenesis in non-demented individuals with AD neuropathology
title_fullStr Preserved neurogenesis in non-demented individuals with AD neuropathology
title_full_unstemmed Preserved neurogenesis in non-demented individuals with AD neuropathology
title_short Preserved neurogenesis in non-demented individuals with AD neuropathology
title_sort preserved neurogenesis in non-demented individuals with ad neuropathology
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4906289/
https://www.ncbi.nlm.nih.gov/pubmed/27298190
http://dx.doi.org/10.1038/srep27812
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