Apolipoprotein-based regulation of ganglioside metabolism upon secretase activity inhibition in iPSC-derived cerebral organoids

Abstract

Beta and gamma-secretase inhibitors have been of pharmacological interest to reduce abeta (A{beta}) formation and aggregation, one of the defining characteristics of Alzheimers disease (AD). Recent research indicates that Apolipoprotein E (ApoE), a genetic risk factor for AD, can regulate secretase activity. Secretase inhibitor-induced elevation of neuronal membrane lipids has been documented in 2D models. Due to their enhanced ability to reproduce AD-like pathology and ease of performing the experimental intervention, we utilized a 3D cerebral organoid model derived from human pluripotent stem cells generated from an AD patient. We treated cerebral organoids carrying ApoE3 and ApoE4 variants with beta and gamma-secretase inhibitors to determine if organoids could reproduce the differences observed in the 2D model and if the alteration in secretase activity could affect the regulation of neuronal lipids synthesis in an ApoE-dependent manner. Ganglioside profiling was accomplished using liquid chromatography/electrospray ionization tandem mass spectrometry (LC/ESI-MS/MS) via selective reaction monitoring (SRM). The inhibitor administration elevated the levels of ganglioside and ceramide in ApoE4-derived organoids. Since gangliosides are known to enhance A{beta} fibrillogenesis, our study implies that reduction in secretase activity affects neuronal membrane architecture that could eventually aggravate AD, particularly in patients with the ApoE4 isoform. In addition, the ability of organoids to replicate results from other experimental models demonstrates their potential to improve translatability significantly.