Published April 29, 2026 | Version v6
Dataset Open

Progressive Vulnerability of Cortical Synapses in α-Synucleinopathy: Dataset

  • 1. ROR icon Yale University
  • 2. Washington University School of Medicine in St. Louis
  • 1. ROR icon Yale University
  • 2. ROR icon University of Alabama at Birmingham
  • 3. Washington University School of Medicine in St. Louis

Description

Tabular data for the following experiments:

Analysis of synaptic localization of pSYN, synaptic density, and association of synaptic pSYN to pSYN positive neurites_AS: Synaptic localization of pSYN, synaptic density, and puncta size changes (relative to Lewy neurites), as well as the association of synaptic pSYN with pSYN-positive neurites, were quantified.

SEQUIN for VGLUT1, VGLUT2 and VGAT positive synaspes_SS: Synaptic loci frequency distributions and synapse densities for VGLUT1- and VGLUT2-positive excitatory synaptic loci and VGAT-positive inhibitory synaptic loci were quantified.

VGLUT1 and VGLUT2 colocalization with endogenous α-synuclein_SS: Colocalization of VGLUT1 and VGLUT2 with endogenous α-synuclein was quantified in the cortex.

Electron Microscopy analysis of excitatory synapses_JR_DR: Ultrastructural measures were quantified, including synaptic vesicle area, intervesicular distance, and synaptic cleft distance.

pSyn pathology negatively impacts excitatory transmission_JG: Electrophysiology data from cortical slices were analyzed to assess how pSyn pathology affects synaptic transmission.

pSyn pathology progressively increases_SS: Lewy pathology progression at 1, 2, and 3 months post–striatal PFF injection was quantified.

 

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Additional details

Funding

Aligning Science Across Parkinson's
Understanding and Manipulating Cellular and Circuit-Level Vulnerability to Neurodegeneration in Parkinson’s disease 020616