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

被引:0
作者
Stein-O'Brien, Genevieve L. [1 ,2 ,8 ]
Palaganas, Ryan [1 ]
Meyer, Ernest M. [3 ]
Redding-Ochoa, Javier [4 ]
Pletnikova, Olga [4 ,5 ]
Guo, Haidan [4 ]
Bell, William R. [6 ,7 ]
Troncoso, Juan C. [4 ,8 ]
Huganir, Richard L. [1 ,2 ]
Morris, Meaghan [2 ,4 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Neurosci, Baltimore, MD 21205 USA
[2] Kavli Neurosci Discovery Inst, Baltimore, MD 21218 USA
[3] Univ Pittsburgh, UPMC Hillman Canc Ctr Cytometry Facil, Pittsburgh, PA 15232 USA
[4] Johns Hopkins Univ, Sch Med, Dept Pathol, Baltimore, MD 21205 USA
[5] Univ Buffalo, Dept Pathol & Anat Sci, Buffalo, NY 14203 USA
[6] Indiana Univ, Sch Med, Dept Pathol, Indianapolis, IN 46202 USA
[7] Indiana Univ, Sch Med, Lab Med, Indianapolis, IN 46202 USA
[8] Johns Hopkins Univ, Sch Med, Dept Neurol, Baltimore, MD 21205 USA
基金
美国国家卫生研究院;
关键词
DIFFERENTIAL EXPRESSION ANALYSIS; NEUROPATHOLOGIC ASSESSMENT; PYRAMIDAL NEURONS; RNA-SEQ; DYSREGULATION; PACKAGE; TANGLES; BRAIN; ATLAS;
D O I
10.1016/j.celrep.2025.115422
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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.
引用
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页数:16
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