TY - JOUR T1 - Precision Mapping of Amyloid-β Binding Reveals Perisynaptic Localization and Spatially Restricted Plasticity Deficits JF - eneuro JO - eNeuro DO - 10.1523/ENEURO.0416-21.2021 SP - ENEURO.0416-21.2021 AU - Hannah S. Actor-Engel AU - Samantha L. Schwartz AU - Kevin C. Crosby AU - Brooke L. Sinnen AU - Olga Prikhodko AU - Harrison J. Ramsay AU - Jennifer N. Bourne AU - Christina S. Winborn AU - Alexandra Lucas AU - Katherine R. Smith AU - Mark L. Dell’Acqua AU - Matthew J. Kennedy Y1 - 2021/11/17 UR - http://www.eneuro.org/content/early/2021/11/17/ENEURO.0416-21.2021.abstract N2 - Secreted amyloid-β (Aβ) peptide forms neurotoxic oligomeric assemblies thought to cause synaptic deficits associated with Alzheimer’s disease (AD). Soluble Aβ oligomers (Aβo) directly bind to neurons with high affinity and block plasticity mechanisms related to learning and memory, trigger loss of excitatory synapses and eventually cause cell death. While Aβo toxicity has been intensely investigated, it remains unclear precisely where Aβo initially binds to the surface of neurons and whether sites of binding relate to synaptic deficits. Here, we used a combination of live cell, super-resolution and ultrastructural imaging techniques to investigate the kinetics, reversibility and nanoscale location of Aβo binding. Surprisingly, Aβo does not bind directly at the synaptic cleft as previously thought but, instead, forms distinct nanoscale clusters encircling the postsynaptic membrane with a significant fraction also binding presynaptic axon terminals. Synaptic plasticity deficits were observed at Aβo-bound synapses but not closely neighboring Aβo-free synapses. Thus, perisynaptic Aβo binding triggers spatially restricted signaling mechanisms to disrupt synaptic function. These data provide new insight into the earliest steps of Aβo pathology and lay the groundwork for future studies evaluating potential surface receptor(s) and local signaling mechanisms responsible for Aβo binding and synapse dysfunction.Significance StatementAmyloid-β (Aβ) is one of the principal neurotoxic agents responsible for Alzheimer’s disease (AD). Defining where Aβ attaches to neurons is critical for understanding its toxicity and role in disease. Here, we used high resolution microscopy techniques to demonstrate Aβ rapidly forms stable nanoscale clusters immediately adjacent to a subset of excitatory synaptic connections. Synaptic plasticity was only impaired at Aβ-targeted synapses and not at neighboring Aβ-free synapses. Thus, perisynaptic Aβ binding rapidly triggers locally restricted signaling mechanisms underlying its synaptic toxicity. ER -