Amyloid beta is released by lysosomal exocytosis from hiPSC-derived neurons
Tsang, A. R.; Medapati, M. R.; Seah, C.; Krupa, J. M.; Pasternak, S. H.
Show abstract
The endosomal-lysosomal system has long been linked to the production of amyloid beta (A{beta}), but the specific intracellular compartments involved in A{beta} secretion remain contentious. While lysosomes are typically associated with A{beta} degradation, studies have also shown that lysosomes also serve as site of A{beta} accumulation in cells, mouse models, and human tissues. Lysosomal exocytosis is a major secretory pathway in non-neuronal cells, but few studies have investigated this pathway in neurons. Here, we examined the potential role and mechanism of lysosomal exocytosis in human induced pluripotent stem cell (hiPSC)-derived neurons, and we hypothesized that lysosomal exocytosis is a pathway for A{beta} secretion from these neurons. Using total internal reflection fluorescence (TIRF) microscopy, lysosomes filled with fluorescently labelled amyloid were seen approaching and fusing with the plasma membrane in real-time. The number and composition of the released particles were characterized using nanoscale flow cytometry. Silencing two proteins, Rab27b and munc13-4, significantly reduced these events and blocked the release of amyloid into the extracellular space. Our results provide direct evidence for the involvement of lysosomal exocytosis in the release of A{beta} from neurons and highlight its potential as a target for therapeutic intervention in Alzheimers disease.
Matching journals
The top 12 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- Atlastin-1 regulates endosomal tubulation and lysosomal proteolysis in human cortical neurons 94%
- Extracellular tau clearance is governed by its aggregation state and independent of microglial activation by LPS and IFN-γ 94%
- Novel extracellular vesicle release pathway facilitated by toxic superoxide dismutase 1 oligomers 94%
Similar papers in this journal
- β-Amyloid Induces Microglial Expression of GPC4 and APOE Leading to Increased Neuronal Tau Pathology and Toxicity 95%
- Amyloid plaque deposition accelerates tau propagation via activation of microglia in a humanized APP mouse model 94%
- Diabetic phenotype in mouse and humans with β-amyloid pathology reduces the number of microglia around β-amyloid plaques 94%
Similar papers in this journal
- Distinct alpha-synuclein strains derived from Parkinson's disease patient tissues trigger differential inclusion pathology in a novel biosensor cell model 95%
- Wild-type sTREM2 blocks Aβ aggregation and neurotoxicity, while the Alzheimer's R47H mutant does the opposite 94%
- Dual fates of exogenous tau seeds: lysosomal clearance vs. cytoplasmic amplification 94%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.