Cargando…
sTREM2 is associated with attenuated tau aggregate accumulation in the presence of amyloid-β pathology
Triggering Receptor Expressed on Myeloid Cell 2 (TREM2) plays a crucial role in the transition of microglia from a state of homeostasis to a state associated with the disease. Mutations in TREM2 are strongly linked with a higher risk of developing neurodegenerative diseases, including Alzheimer’s di...
Autor principal: | |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10629471/ https://www.ncbi.nlm.nih.gov/pubmed/37942087 http://dx.doi.org/10.1093/braincomms/fcad286 |
_version_ | 1785131971875176448 |
---|---|
author | Nabizadeh, Fardin |
author_facet | Nabizadeh, Fardin |
author_sort | Nabizadeh, Fardin |
collection | PubMed |
description | Triggering Receptor Expressed on Myeloid Cell 2 (TREM2) plays a crucial role in the transition of microglia from a state of homeostasis to a state associated with the disease. Mutations in TREM2 are strongly linked with a higher risk of developing neurodegenerative diseases, including Alzheimer’s disease. There have been contradictory findings regarding the potential detrimental or protective effects of microglial activation and TREM2-related microglial responses in Alzheimer’s disease. Although previous studies reported increased CSF soluble TREM2 (sTREM2) in different clinical stages of Alzheimer’s disease, the exact association between Alzheimer’s disease hallmarks such as amyloid-beta and tau pathology remains unclear. In the present study, I aimed to investigate the association between TREM2-related microglial responses and tau accumulation in the presence and absence of amyloid-beta pathology in order to give a better view of the role of microglial activation in Alzheimer’s disease development. Imaging data of 178 non-demented participants including 107 amyloid-beta-negative participants, 71 amyloid-beta-positive were recruited from Alzheimer’s disease Neuroimaging Initiative. The CSF sTREM2 was used as an in vivo indicator of microglial responses associated with TREM2. Furthermore, I used longitudinal tau-PET and resting-state functional MRI connectomes in order to investigate the association of TREM2-related microglial activation and tau spreading through functional connections. A higher level of sTREM2 was associated with slower tau aggregate accumulation in non-demented amyloid-beta-positive. Furthermore, measuring the tau spreading through inter-connected regions using functional MRI connectomes confirms that the TREM2-related microglial activity might be a protective factor against tau pathology in brain tissue. These findings demonstrate that in individuals with initial amyloid-beta abnormalities, TREM2-related microglial activation is linked to reduced regional accumulation of tau aggregates and also, spreading across inter-connected brain regions, as evaluated through functional MRI connectomes during the early stages of Alzheimer’s disease. |
format | Online Article Text |
id | pubmed-10629471 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-106294712023-11-08 sTREM2 is associated with attenuated tau aggregate accumulation in the presence of amyloid-β pathology Nabizadeh, Fardin Brain Commun Original Article Triggering Receptor Expressed on Myeloid Cell 2 (TREM2) plays a crucial role in the transition of microglia from a state of homeostasis to a state associated with the disease. Mutations in TREM2 are strongly linked with a higher risk of developing neurodegenerative diseases, including Alzheimer’s disease. There have been contradictory findings regarding the potential detrimental or protective effects of microglial activation and TREM2-related microglial responses in Alzheimer’s disease. Although previous studies reported increased CSF soluble TREM2 (sTREM2) in different clinical stages of Alzheimer’s disease, the exact association between Alzheimer’s disease hallmarks such as amyloid-beta and tau pathology remains unclear. In the present study, I aimed to investigate the association between TREM2-related microglial responses and tau accumulation in the presence and absence of amyloid-beta pathology in order to give a better view of the role of microglial activation in Alzheimer’s disease development. Imaging data of 178 non-demented participants including 107 amyloid-beta-negative participants, 71 amyloid-beta-positive were recruited from Alzheimer’s disease Neuroimaging Initiative. The CSF sTREM2 was used as an in vivo indicator of microglial responses associated with TREM2. Furthermore, I used longitudinal tau-PET and resting-state functional MRI connectomes in order to investigate the association of TREM2-related microglial activation and tau spreading through functional connections. A higher level of sTREM2 was associated with slower tau aggregate accumulation in non-demented amyloid-beta-positive. Furthermore, measuring the tau spreading through inter-connected regions using functional MRI connectomes confirms that the TREM2-related microglial activity might be a protective factor against tau pathology in brain tissue. These findings demonstrate that in individuals with initial amyloid-beta abnormalities, TREM2-related microglial activation is linked to reduced regional accumulation of tau aggregates and also, spreading across inter-connected brain regions, as evaluated through functional MRI connectomes during the early stages of Alzheimer’s disease. Oxford University Press 2023-10-24 /pmc/articles/PMC10629471/ /pubmed/37942087 http://dx.doi.org/10.1093/braincomms/fcad286 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of the Guarantors of Brain. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Nabizadeh, Fardin sTREM2 is associated with attenuated tau aggregate accumulation in the presence of amyloid-β pathology |
title | sTREM2 is associated with attenuated tau aggregate accumulation in the presence of amyloid-β pathology |
title_full | sTREM2 is associated with attenuated tau aggregate accumulation in the presence of amyloid-β pathology |
title_fullStr | sTREM2 is associated with attenuated tau aggregate accumulation in the presence of amyloid-β pathology |
title_full_unstemmed | sTREM2 is associated with attenuated tau aggregate accumulation in the presence of amyloid-β pathology |
title_short | sTREM2 is associated with attenuated tau aggregate accumulation in the presence of amyloid-β pathology |
title_sort | strem2 is associated with attenuated tau aggregate accumulation in the presence of amyloid-β pathology |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10629471/ https://www.ncbi.nlm.nih.gov/pubmed/37942087 http://dx.doi.org/10.1093/braincomms/fcad286 |
work_keys_str_mv | AT nabizadehfardin strem2isassociatedwithattenuatedtauaggregateaccumulationinthepresenceofamyloidbpathology |