Journal
JOURNAL OF NEUROSCIENCE
Volume 34, Issue 6, Pages 2037-2050Publisher
SOC NEUROSCIENCE
DOI: 10.1523/JNEUROSCI.2581-13.2014
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Funding
- National Institutes of Health [NS069625, AG024978, AT002688, NS061800]
- Department of Veterans Affairs Merit Review Award
- Murdock Charitable Trust
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Parkinson's disease and dementia with Lewy bodies are associated with abnormal neuronal aggregation of alpha-synuclein. However, the mechanisms of aggregation and their relationship to disease are poorly understood. We developed an in vivo multiphoton imaging paradigm to study alpha-synuclein aggregation in mouse cortex with subcellular resolution. We used a green fluorescent protein-tagged human alpha-synuclein mouse line that has moderate overexpression levels mimicking human disease. Fluorescence recovery after photobleaching (FRAP) of labeled protein demonstrated that somatic alpha-synuclein existed primarily in an unbound, soluble pool. In contrast, alpha-synuclein in presynaptic terminals was in at least three different pools: (1) as unbound, soluble protein; (2) bound to presynaptic vesicles; and (3) as microaggregates. Serial imaging of microaggregates over 1 week demonstrated a heterogeneous population with differing alpha-synuclein exchange rates. The microaggregate species were resistant to proteinase K, phosphorylated at serine-129, oxidized, and associated with a decrease in the presynaptic vesicle protein synapsin and glutamate immunogold labeling. Multiphoton FRAP provided the specific binding constants for alpha-synuclein's binding to synaptic vesicles and its effective diffusion coefficient in the soma and axon, setting the stage for future studies targeting synuclein modifications and their effects. Our in vivo results suggest that, under moderate overexpression conditions, alpha-synuclein aggregates are selectively found in presynaptic terminals.
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