Abstract
Optical imaging is a valuable tool for investigating alterations in membrane turnover and vesicle trafficking. Established techniques can easily be adapted to study the mechanisms of synaptic dysfunction in models of neuropsychiatric disorders and neurodegenerative diseases, such as drug addiction, Parkinsonism, and Huntington’s disease. Fluorescent endocytic tracers, including FM1-43, have been used to optically monitor synaptic vesicle fusion and measure synaptic function in various preparations, including chromaffin cells, dissociated cell cultures, and brain slices. In this chapter, we describe a technique that provides a direct measure of pathway-specific exocytosis from glutamatergic corticostriatal terminals.
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Acknowledgments
This work was supported by DA07418, Picower and Parkinson’s Disease Foundations (DS) and by NS052536, NS060803, HD02274, University of Washington Vision Research Center and Children’s Hospital, Seattle, WA (NSB).
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Wong, M.Y., Sulzer, D., Bamford, N.S. (2011). Imaging Presynaptic Exocytosis in Corticostriatal Slices. In: Manfredi, G., Kawamata, H. (eds) Neurodegeneration. Methods in Molecular Biology, vol 793. Humana Press, Totowa, NJ. https://doi.org/10.1007/978-1-61779-328-8_24
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DOI: https://doi.org/10.1007/978-1-61779-328-8_24
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