The broad, long-term objective of the research proposed in this application is to understand the cellular and molecular mechanisms that determine how synapses work. One of the most complex events occurring in a synapse is the synaptic vesicle cycle. Some aspects of the cycle are understood in molecular detail;the least understood aspect concerns the mobilization of synaptic vesicles, that is, their movement from deep in the cytoplasm to the presynaptic membrane as a prelude to docking and exocytosis.
The Specific Aims of this proposal are to monitor the movements of synaptic vesicles in living synapses, and identify the molecular mechanisms that regulate.the motion. .. ... We will directly monitor synaptic vesicle movements in motor nerve terminals of the neuromuscular junction (NMJ). We will selectively label distinct vesicle pools in living nerve terminals with fluorescent (FM) dyes, and monitor vesicle movements at rest, during nerve stimulation, and after applying drugs that interfere with specific signaling pathways. We will study frog and mouse NMJs. The frog NMJ is useful because it is one of the best understood synapses, and it is optimally suited for developing and refining the measuring techniques that we will use. The mouse NMJ offers the opportunity to examine genetic knockouts; we will focus in particular on The Synapsin Hypothesis, by comparing vesicle mobilization in synapsin knockout and wild type mice. The techniques that we will use include electrophysiology, electron microscopy, and especially fluorescence microscopy. Both Fluorescence Recovery After Photobleaching (FRAP) and Image Correlation Spectroscopy (ICS) will be employed to quantify vesicle mobilization. Implications for human health: Synapses are like transistors in a computer - the points at which converging information is sorted and analyzed. A synapse is far more complex, however, than a transistor, comprising thousands of different molecules, and even moving parts (the subject of our research). Nearly all therapeutic psychoactive drugs act at synapses. A better understanding of the fundamental mechanisms of vesicle recycling will be useful in understanding diseases of the nervous system, and in developing better drug therapies.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS023466-21
Application #
7586129
Study Section
Synapses, Cytoskeleton and Trafficking Study Section (SYN)
Program Officer
Talley, Edmund M
Project Start
1986-07-01
Project End
2011-04-30
Budget Start
2009-05-01
Budget End
2011-04-30
Support Year
21
Fiscal Year
2009
Total Cost
$329,153
Indirect Cost
Name
University of Colorado Denver
Department
Physiology
Type
Schools of Medicine
DUNS #
041096314
City
Aurora
State
CO
Country
United States
Zip Code
80045
Gaffield, Michael A; Romberg, Christin F; Betz, William J (2011) Live imaging of bulk endocytosis in frog motor nerve terminals using FM dyes. J Neurophysiol 106:599-607
Gaffield, Michael A; Tabares, Lucia; Betz, William J (2009) The spatial pattern of exocytosis and post-exocytic mobility of synaptopHluorin in mouse motor nerve terminals. J Physiol 587:1187-200
Gaffield, Michael A; Tabares, Lucia; Betz, William J (2009) Preferred sites of exocytosis and endocytosis colocalize during high- but not lower-frequency stimulation in mouse motor nerve terminals. J Neurosci 29:15308-16
Rizzoli, Silvio O; Betz, William J (2004) The structural organization of the readily releasable pool of synaptic vesicles. Science 303:2037-9
Brumback, Audrey C; Lieber, Janet L; Angleson, Joseph K et al. (2004) Using FM1-43 to study neuropeptide granule dynamics and exocytosis. Methods 33:287-94
Rizzoli, Silvio O; Richards, David A; Betz, William J (2003) Monitoring synaptic vesicle recycling in frog motor nerve terminals with FM dyes. J Neurocytol 32:539-49
Rizzoli, Silvio O; Betz, William J (2002) Effects of 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one on synaptic vesicle cycling at the frog neuromuscular junction. J Neurosci 22:10680-9
Adlard, K; Tsaknardis, L; Beam, A et al. (1999) Immunoregulation of encephalitogenic MBP-NAc1-11-reactive T cells by CD4+ TCR-specific T cells involves IL-4, IL-10 and IFN-gamma. Autoimmunity 31:237-48
Wu, L G; Betz, W J (1996) Nerve activity but not intracellular calcium determines the time course of endocytosis at the frog neuromuscular junction. Neuron 17:769-79
Henkel, A W; Simpson, L L; Ridge, R M et al. (1996) Synaptic vesicle movements monitored by fluorescence recovery after photobleaching in nerve terminals stained with FM1-43. J Neurosci 16:3960-7

Showing the most recent 10 out of 24 publications