If a skeletal muscle and/or its motor nerve is damaged, neuromuscular function ceases. With time, muscle fibers regenerate, the portions of the axons that remain connected to the central nervous system grow to them, and neuromuscular function is restored. Recovery of function, however, is seldom complete. A pianist who severs a nerve to muscles of the hand can regain use of the hand for moving objects but will never perform again. Studies on specific aspects of regeneration in situations where they can be examined in detail are requisite for devising ways to enhance functional recovery in the neuromuscular system after damage resulting from disease or trauma. The long-range objectives of this project are to identify structures in nerve and muscle that influence regeneration of the neuromuscular junction and to determine what sorts of information they provide.
The specific aims of the experiments outlined in this project are to: a) characterize the influence of Schwann cells and their basal lamina sheaths on the direction of growth of regenerating axons; b) to examine the influence of tissue components other than myofibers on the differentiation and maintenance of regenerating axon terminals; c) to characterize the role of tissue components other than axon terminals on the development of the postsynaptic apparatus in regenerating myofibers; and d) to identify and characterize specific molecules involved in regeneration of the neuromuscular junction. These experiments will be conducted under in vivo and in vivo situations. They will involve a variety of surgical, light and electron microscopical, biochemical, immunochemical and cell biological techniques. The vertebrates involved in the experiments will be frogs, rats, mice and Torpedo Californica.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS014506-13
Application #
3395591
Study Section
Neurology B Subcommittee 1 (NEUB)
Project Start
1979-04-01
Project End
1991-03-31
Budget Start
1989-04-01
Budget End
1990-03-31
Support Year
13
Fiscal Year
1989
Total Cost
Indirect Cost
Name
Stanford University
Department
Type
Schools of Medicine
DUNS #
800771545
City
Stanford
State
CA
Country
United States
Zip Code
94305
Jung, Jae H; Szule, Joseph A; Stouder, Kylee et al. (2018) Active Zone Material-Directed Orientation, Docking, and Fusion of Dense Core Vesicles Alongside Synaptic Vesicles at Neuromuscular Junctions. Front Neuroanat 12:72
Jung, Jae Hoon; Szule, Joseph A; Marshall, Robert M et al. (2016) Variable priming of a docked synaptic vesicle. Proc Natl Acad Sci U S A 113:E1098-107
Szule, Joseph A; Jung, Jae Hoon; McMahan, Uel J (2015) The structure and function of 'active zone material' at synapses. Philos Trans R Soc Lond B Biol Sci 370:
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Szule, Joseph A; Harlow, Mark L; Jung, Jae Hoon et al. (2012) Regulation of synaptic vesicle docking by different classes of macromolecules in active zone material. PLoS One 7:e33333
Nagwaney, Sharuna; Harlow, Mark Lee; Jung, Jae Hoon et al. (2009) Macromolecular connections of active zone material to docked synaptic vesicles and presynaptic membrane at neuromuscular junctions of mouse. J Comp Neurol 513:457-68
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Mathiesen, I; Rimer, M; Ashtari, O et al. (1999) Regulation of the size and distribution of agrin-induced postsynaptic-like apparatus in adult skeletal muscle by electrical muscle activity. Mol Cell Neurosci 13:207-17
Ress, D; Harlow, M L; Schwarz, M et al. (1999) Automatic acquisition of fiducial markers and alignment of images in tilt series for electron tomography. J Electron Microsc (Tokyo) 48:277-87
Rimer, M; Cohen, I; Lomo, T et al. (1998) Neuregulins and erbB receptors at neuromuscular junctions and at agrin-induced postsynaptic-like apparatus in skeletal muscle. Mol Cell Neurosci 12:1-15

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