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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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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. |
format | Online Article Text |
id | pubmed-4906289 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
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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