Isotope-encoded spatial biology identifies plaque-age-dependent maturation and synaptic loss in an Alzheimer’s disease mouse model

Understanding how amyloid beta (Aβ) plaques develop and lead to neurotoxicity in Alzheimer's disease remains a major challenge, particularly given the temporal delay and weak correlation between plaque deposition and cognitive decline. This study investigates how the evolving pathology of plaques affects the surrounding tissue, using a knock-in Aβ mouse model (App<sup>NL-F/NL-F</sup>). We combined mass spectrometry imaging with stable isotope labeling to timestamp Aβ plaques from the moment of their initial deposition, enabling us to track their aging spatially. By integrating spatial transcriptomics, we linked changes in gene expression to the age of the plaques, independent of the mice's chronological age or disease stage. Here we show that older plaques were associated with reduced expression of synaptic genes. Additionally, when correlated with structure-specific dyes, we show that plaque age positively correlated with structural maturation. These more compact and older plaques were linked to greater synapse loss and increased toxicity.

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Publication Details

Journal
Nature Communications
Published
2025-09-01
DOI
https://doi.org/10.1038/s41467-025-63328-y
Citations
1
Primary Topic
Alzheimer's disease research and treatments
Type
article
Field-Weighted Citation Impact
1.16

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article

Isotope-encoded spatial biology identifies plaque-age-dependent maturation and synaptic loss in an Alzheimer’s disease mouse model

Gunnar Brinkmalm, Jörg Hanrieder, Sneha Desai, Alicja Szadziewska et al.
1 citations
Nature Communications
Alzheimer's disease research and treatments
1.16
article

Isotope-encoded spatial biology identifies plaque-age-dependent maturation and synaptic loss in an Alzheimer’s disease mouse model

Gunnar Brinkmalm, Jörg Hanrieder, Sneha Desai, Alicja Szadziewska, Kaj Blennow, Sophia Weiner, Jack I. Wood, Katie Stringer, Diana Piotrowska, Damian M. Cummings, Jeffrey N. Savas, Frances A. Edwards, Maciej Dulewicz, Srinivas Koutarapu, Junyue Ge, Henrik Zetterberg, Haady B. Hajar, Lydia Fenson
article en
1 citations

Abstract

Understanding how amyloid beta (Aβ) plaques develop and lead to neurotoxicity in Alzheimer's disease remains a major challenge, particularly given the temporal delay and weak correlation between plaque deposition and cognitive decline. This study investigates how the evolving pathology of plaques affects the surrounding tissue, using a knock-in Aβ mouse model (App<sup>NL-F/NL-F</sup>). We combined mass spectrometry imaging with stable isotope labeling to timestamp Aβ plaques from the moment of their initial deposition, enabling us to track their aging spatially. By integrating spatial transcriptomics, we linked changes in gene expression to the age of the plaques, independent of the mice's chronological age or disease stage. Here we show that older plaques were associated with reduced expression of synaptic genes. Additionally, when correlated with structure-specific dyes, we show that plaque age positively correlated with structural maturation. These more compact and older plaques were linked to greater synapse loss and increased toxicity.

Nature CommunicationsVol. 16(1)
Northwestern University (US), University of Science and Technology of China (CN), University of Wisconsin–Madison (US), Sahlgrenska University Hospital (SE), Sorbonne Université (FR), Pitié-Salpêtrière Hospital (FR), UK Dementia Research Institute (GB), MRC Prion Unit (GB), NIHR Queen Square Dementia Biomedical Research Unit (GB), Institut du Cerveau (FR), University College London (GB), University of Gothenburg (SE)
National Institutes of Health
Openalex Percentile: Top 18%
Alzheimer's disease research and treatments
1.16
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