Characterization and pharmacological modulation of Alzheimer’s disease-associated human microglial states
TL;DR
This work integrated single-nucleus transcriptomic datasets across the AD spectrum and identified DLaM as a major AD-enriched population linked to genetic risk, neuropathology and cognitive decline, and identified LY2090314 as a potent modulator that restored microglial function and induced a distinct lysosomal-metabolic state.
Abstract
Microglia are central mediators of Alzheimer’s disease (AD) pathogenesis, yet the mechanisms driving disease-associated microglial states and their therapeutic modulation remain poorly understood. Here, we integrated single-nucleus transcriptomic datasets across the AD spectrum and identified disease- and lipid-associated microglia (DLaM) as a major AD-enriched population linked to genetic risk, neuropathology and cognitive decline. To model this state experimentally, we screened AD-relevant perturbations in human induced pluripotent stem cell (hiPSC)-derived microglia and found that ferric ammonium citrate (FAC) reproducibly induced a DLaM-like state characterized by lipid accumulation, lysosomal dysfunction and impaired Aβ phagocytosis. Using a transcriptomics-based state-reversion screen, we identified LY2090314 as a potent modulator that restored microglial function and induced a distinct lysosomal-metabolic state. These findings establish a framework for transcriptomic disease-state-guided therapeutic discovery in AD.