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Live Cell FRET Imaging Reveals Amyloid β-Peptide Oligomerization in Hippocampal Neurons

Yang Gao, Stefan Wennmalm, Bengt Winblad, Sophia Schedin‐Weiss, Lars O. Tjernberg

2021International Journal of Molecular Sciences10 citationsDOIOpen Access PDF

Abstract

Amyloid β-peptide (Aβ) oligomerization is believed to contribute to the neuronal dysfunction in Alzheimer disease (AD). Despite decades of research, many details of Aβ oligomerization in neurons still need to be revealed. Förster resonance energy transfer (FRET) is a simple but effective way to study molecular interactions. Here, we used a confocal microscope with a sensitive Airyscan detector for FRET detection. By live cell FRET imaging, we detected Aβ42 oligomerization in primary neurons. The neurons were incubated with fluorescently labeled Aβ42 in the cell culture medium for 24 h. Aβ42 were internalized and oligomerized in the lysosomes/late endosomes in a concentration-dependent manner. Both the cellular uptake and intracellular oligomerization of Aβ42 were significantly higher than for Aβ40. These findings provide a better understanding of Aβ42 oligomerization in neurons.

Topics & Concepts

Förster resonance energy transferEndosomeIntracellularConfocal microscopyCell biologyAmyloid (mycology)BiophysicsChemistryPeptideHippocampal formationCellBiologyNeuroscienceBiochemistryFluorescenceQuantum mechanicsPhysicsInorganic chemistryAlzheimer's disease research and treatmentsNeuroscience and Neuropharmacology ResearchDrug Transport and Resistance Mechanisms