Progressive vulnerability of cortical synapses in α-synucleinopathy

Output Details

Preprint September 6, 2024

α-Synuclein aggregation is a hallmark of Parkinson’s disease and dementia with Lewy bodies, where cortical pathology is closely linked to cognitive decline. Although synaptic dysfunction is a recognized feature of α-synucleinopathy, the selective vulnerability and spatial progression of specific cortical synapse subtypes remain unclear. Using high-resolution imaging and electron microscopy in a mouse model, we show synaptic enrichment of α-synuclein aggregates, with progressive pathology associated with loss and ultrastructural alterations of intracortical VGLUT1+ excitatory synapses, while long-range VGLUT2+ synapses remain largely preserved. Inhibitory VGAT+ synapses exhibit modest late-stage postsynaptic disruption. Electrophysiological recordings confirm impaired excitatory transmission. Transcriptomic profiling reveals altered synapse-related pathways and candidate resilience mechanisms in affected neurons. These findings highlight synapse-type-specific vulnerabilities and establish VGLUT1+  intracortical excitatory synapses as critical sites of disrupted cortical connectivity in α-synucleinopathy.
Tags
  • Alpha-synuclein
  • Electron microscopy
  • Electrophysiology
  • Ex Vivo
  • Immunohistochemistry
  • In Vivo
  • Mouse
  • Pre-formed fibrils (PFFs)
  • Synapse
  • Synaptic dysfunction

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