HOPS disruption impairs APP trafficking and processing, promoting exosomal secretion of APP-CTFs

Amyloid precursor protein (APP) is a key player in various neuronal functions but also the source for toxic A{beta} that accumulates in the brain of Alzheimer patients. APP trafficking and processing depend on the endo-lysosomal system, but the molecular mechanisms that coordinate these processes remain unclear. Here, we studied the HOPS complex, a central regulator of endo-lysosomal maturation. We show that HOPS disruption impairs retromer-mediated recycling of APP to the TGN, resulting in the accumulation of APP in late endosomes. In neurons, this accumulation is spatially restricted to somatodendritic endosomes. These APP-containing endosomes are catalytically inactive and lack the {gamma}-secretase subunit PSEN2. However, they do contain BACE1, which leads to the build-up of toxic APP C-terminal fragments (APP-CTFs) upon HOPS disruption. Notably, loss of HOPS enhances secretion of APP-CTFs by exosomes, suggesting a potential mechanism for disease propagation. Together, our findings establish a mechanistic link between HOPS dysfunction and aberrant APP processing, with implications for neurodegeneration. HighlightsO_LIHOPS KO impairs retromer-mediated APP recycling to the TGN C_LIO_LIHOPS disruption redistributes APP to somatodendritic stationary late endosomes C_LIO_LIHOPS depletion increases APP and BACE1 convergence, causing APP-CTF accumulation C_LIO_LIThese APP-CTFs accumulate in catalytically inactive endosomes that lack PSEN2 C_LIO_LIAPP-CTFs are secreted via exosomes, potentially promoting disease propagation C_LI