Research on synaptic vesicles (SVs) has been dominated for many years by studies that have focused on mechanisms for their exocytosis and endocytosis. By comparison, relatively little has been learned about the subject of this competitive renewal application, the trafficking of SVs in the axon terminal. The proposal is focused on two morphologically and functionally distinct populations of SVs, the readily releasable and reserve pools, and on the role of actin in SV recycling. The planned experiments are based on three technical advances that were made during the present funding period. 1) Several years ago, Dr. Betz pioneered the use of fluorescent FM dyes as tools for labeling SVs in axon terminals. Much more recently, he developed a method for converting DAB into an insoluble, electron dense product following photoactivation of FM dyes. This method leads to very high resolution labeling of individual SVs and putative SV recycling cisternae at the EM level. 2) An EM method for discriminating readily releasable SVs from the reserve pool of SVs has been developed. The method relies on FM dye photoactivation, and the distinct properties of two such dyes, FM1-43 and FM2-10. Apparently, FM1-43 labels both SV pools, whereas the less hydrophobic FM2-10 selectively labels the readily releasable population. 3) Two pools of actin are located in motor neuron synapses: beta-actin is confined to axon terminals, whereas alpha-actin is restricted to skeletal muscle fibers. Using an antibody specific for beta-actin, Dr. Betz has been able to achieve selective immunofluorescent labeling of the actin present in axon terminals, without interference from the nearby, intensely actin-rich muscle fibers. Using this approach, he has found that in resting axon terminals actin is localized in a ladder-like pattern which is complementary to where clusters of SVs are localized, but following prolonged nerve stimulation the actin adopts a more diffuse distribution. Dr. Betz interprets these results to indicate that actin is critically invoved in SV trafficking.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS023466-15
Application #
6531035
Study Section
Special Emphasis Panel (ZRG1-MDCN-1 (01))
Program Officer
Nichols, Paul L
Project Start
1986-07-01
Project End
2005-02-28
Budget Start
2002-03-01
Budget End
2003-02-28
Support Year
15
Fiscal Year
2002
Total Cost
$299,899
Indirect Cost
Name
University of Colorado Denver
Department
Physiology
Type
Schools of Medicine
DUNS #
065391526
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

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