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Neuronal activity and amyloid-beta cause tau seeding in the entorhinal cortex in Alzheimer's disease

Alexandersen, C. G. G.; Bassett, D.; Goriely, A.; Chaggar, P.

2025-03-10 neuroscience
10.1101/2025.03.07.642054 bioRxiv
Show abstract

The entorhinal cortex is the earliest site of tau pathology in both Alzheimers disease and primary age-related tauopathy, yet the mechanisms underlying this selective vulnerability remain poorly understood. Here, we use a computational model integrating neuronal activity and amyloid-{beta} deposition with interneuronal tau transport to predict regional susceptibility to tau seeding. Using fluorodeoxyglucose PET as a measure of neuronal activity, we show that brain-wide activity patterns drive tau accumulation in the medial temporal lobe, independent of amyloid status. Incorporating amyloid PET, we further show that amyloid-{beta} selectively amplifies tau seeding in the entorhinal cortex, aligning with its early involvement in Alzheimers disease. These predictions are supported by cross-subject correlation analysis, which reveals a significant association between model-derived seeding concentrations and empirical tau deposition. Our findings suggest that neuronal activity patterns shape the early landscape of tau pathology, while amyloid-{beta} deposition creates a unique vulnerability in the entorhinal cortex, potentially triggering the pathological cascade that defines Alzheimers disease.

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