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BIOLOGICAL SCIENCES / NEUROSCIENCE
Vesicle association and exocytosis at ribbon and extraribbon sites in retinal bipolar cell presynaptic terminals
Department of Cellular and Molecular Physiology, Department of Ophthalmology and Visual Science, Program in Cellular Neuroscience, Neurodegeneration and Repair, Yale University School of Medicine, 333 Cedar Street, SHM-B147, New Haven, CT 06520
Edited by William Betz, University of Colorado School of Medicine, Denver, CO, and accepted by the Editorial Board, accepted February 6, 2008 (received for review September 24, 2007)
Synaptic vesicles release neurotransmitter by following a process of vesicle docking and exocytosis. Although these steps are well established, it has been difficult to observe and measure these rates directly in living synapses. Here, by combining the direct imaging of single synaptic vesicles and synaptic ribbons, I measure the properties of vesicle docking and evoked and spontaneous release from ribbon and extraribbon locations in a ribbon-type synaptic terminal, the goldfish retinal bipolar cell. In the absence of a stimulus, captured vesicles near ribbons associate tightly and only rarely undock or undergo spontaneous exocytosis. By contrast, vesicle capture at outlier sites is less stable and spontaneous exocytosis occurs at a higher rate. In response to a stimulus, exocytic events cluster near ribbons, but show no evidence of clustering away from ribbon sites. Together, the results here indicate that, although vesicles can associate and fuse both near and away from synaptic sites, vesicles at synaptic ribbons associate more stably and fusion is more tightly linked to stimuli.
imaging | neurotransmitter release | retina | synapse | synaptic vesicle
The author declares no conflict of interest.
This article is a PNAS Direct Submission. W.B. is a guest editor invited by the Editorial Board.
*To whom correspondence should be addressed. E-mail: david.zenisek{at}yale.edu
© 2008 by The National Academy of Sciences of the USA
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