Ethanol induces neuroimmune dysregulation and soluble TREM2 generation in a human iPSC neuron, astrocyte, microglia triculture model

ABSTRACT: Alcohol use disorders (AUDs) affect substantial populations worldwide and increase the risk of developing cognitive impairments and alcohol-associated dementia. While the precise mechanisms underlying alcohol-associated neuropathology remain enigmatic, chronic inflammatory signaling likely plays an important role in alcohol-associated neurological sequalae. We hypothesize that alcohol leads to neuroimmune dysregulation among neurons, astrocytes, and microglia; and is perpetuated by innate immune signaling pathways involving cell-cell signaling. To investigate how alcohol dysregulates neuroimmune interactions in a human context, we constructed a triculture model comprising neurons, astrocytes, and microglia derived from human induced pluripotent stem cells (hiPSCs). After exposure to ethanol, we observed significant differential gene expression relating to innate immune pathways, inflammation, and microglial activation. Microglial activation was confirmed with morphological analysis and expression of CD68, a lysosomal-associated membrane protein and marker for phagocytic microglial activation. A striking finding in our study was the elevation of TREM2 expression and, specifically, TREM2 alternative splice variants that are predicted to give rise to soluble TREM2. These results suggest that ethanol exposure in the brain may lead to increased microglial activation and production of soluble TREM2219isoform through alternate splicing. Deciphering the molecular and cellular mechanisms underpinning ethanol-related neuroimmune dysregulation within a human context promises to shed light on the etiology of AUD and AUD-associated dementia, potentially driving the development of effective therapeutic strategies.

ORGANISM(S): Homo sapiens

PROVIDER: GSE303551 | GEO | 2025/08/04

REPOSITORIES: GEO