Transcriptional signatures of hippocampal tau pathology in primary age-related tauopathy and Alzheimer’s disease

In primary age-related tauopathy (PART) and Alzheimer's disease (AD), tau aggregates share a similar structure and anatomic distribution, which is distinct from tau pathology in other diseases. However, transcriptional similarities between PART and AD and gene expression changes within tau-pathology-bearing neurons are largely unknown. Using GeoMx spatial transcriptomics, mRNA was quantified in hippocampal neurons with and without tau pathology in PART and AD. Synaptic genes were down-regulated in disease overall but up-regulated in tau-pathology-positive neurons. Two transcriptional signatures were associated with intraneuronal tau, both validated in a cortical AD dataset. Genes in the up-regulated signature were enriched in calcium regulation and synaptic function. Notably, transcriptional changes associated with intraneuronal tau in PART and AD were similar, suggesting a possible mechanistic relationship. These findings highlight the power of molecular analysis stratified by pathology and provide insight into common pathways associated with tau pathology in PART and AD.

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Publication Details

Journal
Cell Reports
Published
2025-03-01
DOI
https://doi.org/10.1016/j.celrep.2025.115422
Citations
8
Primary Topic
Alzheimer's disease research and treatments
Type
article
Field-Weighted Citation Impact
9.31

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article

Transcriptional signatures of hippocampal tau pathology in primary age-related tauopathy and Alzheimer’s disease

Javier Redding‐Ochoa, Meaghan Morris, Juan C. Troncoso, Richard L. Huganir et al.
8 citations
Cell Reports
Alzheimer's disease research and treatments
9.31
article

Transcriptional signatures of hippocampal tau pathology in primary age-related tauopathy and Alzheimer’s disease

Javier Redding‐Ochoa, Meaghan Morris, Juan C. Troncoso, Richard L. Huganir, Genevieve Stein-O’Brien, William R. Bell, Ryan G. Palaganas, Olga Pletnikova, Haidan Guo, E. Michael Meyer
article en
8 citations

Abstract

In primary age-related tauopathy (PART) and Alzheimer's disease (AD), tau aggregates share a similar structure and anatomic distribution, which is distinct from tau pathology in other diseases. However, transcriptional similarities between PART and AD and gene expression changes within tau-pathology-bearing neurons are largely unknown. Using GeoMx spatial transcriptomics, mRNA was quantified in hippocampal neurons with and without tau pathology in PART and AD. Synaptic genes were down-regulated in disease overall but up-regulated in tau-pathology-positive neurons. Two transcriptional signatures were associated with intraneuronal tau, both validated in a cortical AD dataset. Genes in the up-regulated signature were enriched in calcium regulation and synaptic function. Notably, transcriptional changes associated with intraneuronal tau in PART and AD were similar, suggesting a possible mechanistic relationship. These findings highlight the power of molecular analysis stratified by pathology and provide insight into common pathways associated with tau pathology in PART and AD.

Cell ReportsVol. 44(3)
Johns Hopkins University (US), Johns Hopkins Medicine (US), Neuroscience Institute (IT), UPMC Hillman Cancer Center (US), Indiana University School of Medicine, Indiana University – Purdue University Indianapolis (US), University at Buffalo, State University of New York (US)
Université Pierre et Marie Curie, National Institutes of Health, National Institute on Aging, National Cancer Institute, National Institute of Neurological Disorders and Stroke
Openalex Percentile: Top 2%
Alzheimer's disease research and treatments
9.31
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