Phagocytes as plaque catalysts: Human macrophages generate seeding-competent Aβ42 fibrils with cross-seeding activity

The prevailing view frames microglia and macrophages as guardians against amyloid beta (Aβ) accumulation in Alzheimer's disease (AD). Here, we overturn this paradigm by demonstrating that human phagocytic cells, including differentiated THP-1 macrophages and hESC-derived microglia, are not merely passive responders but active producers of extracellular, seeding-competent Aβ42 fibrils, the amyloid species most strongly linked to parenchymal plaque formation and neurodegeneration. These cell-generated aggregates differ structurally and functionally from synthetic fibrils, displaying enhanced seeding and tau cross-seeding activity in biosensor models. Notably, Aβ42 fibril formation in this system requires active cellular processes and is exacerbated by loss of Triggering Receptor Expressed on Myeloid Cells 2 (TREM2), a major AD risk gene. Transcriptomic profiling reveals an early inflammatory response resembling microglial states observed in human AD models. Together, these findings support emerging evidence from in vivo studies that macrophages and microglia can influence amyloid seeding and introduce a human-relevant in vitro platform to explore how Aβ aggregation intersects with innate immune function and genetic risk. Our results reinforce the concept that microglia may play a dual role in AD, acting both as responders and inadvertent facilitators of amyloid assembly, with implications for early therapeutic intervention.

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Publication Details

Journal
Proceedings of the National Academy of Sciences
Published
2026-03-02
DOI
https://doi.org/10.1073/pnas.2516774123
Primary Topic
Neuroinflammation and Neurodegeneration Mechanisms
Type
article
Field-Weighted Citation Impact
0.00
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article

Phagocytes as plaque catalysts: Human macrophages generate seeding-competent Aβ42 fibrils with cross-seeding activity

Katerina Konstantoulea, Daan Moechars, Giulia Albertini, Rodrigo Gallardo et al.
Proceedings of the National Academy of Sciences
Neuroinflammation and Neurodegeneration Mechanisms
article

Phagocytes as plaque catalysts: Human macrophages generate seeding-competent Aβ42 fibrils with cross-seeding activity

Katerina Konstantoulea, Daan Moechars, Giulia Albertini, Rodrigo Gallardo, Dries T’Syen, Dietmar Rudolf Thal, Meine Ramakers, Joost Schymkowitz, Mark Fiers, Brajabandhu Pradhan, Grigoria Tsaka, Bert Houben, Sarah C. Borrie, Nóra Baligács, Malgorzata Alicja Sliwinska, Frederic Rousseau, Maarten Dewilde, Jonas Neher, Bart De Strooper, Michael Willem
article en

Abstract

The prevailing view frames microglia and macrophages as guardians against amyloid beta (Aβ) accumulation in Alzheimer's disease (AD). Here, we overturn this paradigm by demonstrating that human phagocytic cells, including differentiated THP-1 macrophages and hESC-derived microglia, are not merely passive responders but active producers of extracellular, seeding-competent Aβ42 fibrils, the amyloid species most strongly linked to parenchymal plaque formation and neurodegeneration. These cell-generated aggregates differ structurally and functionally from synthetic fibrils, displaying enhanced seeding and tau cross-seeding activity in biosensor models. Notably, Aβ42 fibril formation in this system requires active cellular processes and is exacerbated by loss of Triggering Receptor Expressed on Myeloid Cells 2 (TREM2), a major AD risk gene. Transcriptomic profiling reveals an early inflammatory response resembling microglial states observed in human AD models. Together, these findings support emerging evidence from in vivo studies that macrophages and microglia can influence amyloid seeding and introduce a human-relevant in vitro platform to explore how Aβ aggregation intersects with innate immune function and genetic risk. Our results reinforce the concept that microglia may play a dual role in AD, acting both as responders and inadvertent facilitators of amyloid assembly, with implications for early therapeutic intervention.

Proceedings of the National Academy of SciencesVol. 123(10)
Allen Institute for Brain Science (US), German Center for Neurodegenerative Diseases (DE), VIB-KU Leuven Center for Cancer Biology (BE), Munich Cluster for Systems Neurology (DE), Research & Diagnostic Antibodies (United States) (US), VIB-KU Leuven Center for Brain & Disease Research (BE), Ludwig-Maximilians-Universität München (DE), KU Leuven (BE), Core Laboratories (United States) (US)
Openalex Percentile: Top 50%
Neuroinflammation and Neurodegeneration Mechanisms
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