Project 4 Every year almost 100,000 people suffer permanent disability from a traumatic brain or spinal cord injury. Over 5 million people with permanent disability are alive today. A major goal of neuroscience research is to understand and promote mechanisms that allow recovery after nervous system injury. Spared neurons react adversely to the injury, or try to compensate for the injury. Unfortunately, even recovery mechanisms can produce unintended consequences, such as spasticity after spinal cord injury, or epilepsy after a cortical brain injury. These anomalous behaviors are due to changes in the functions of individual neurons. Synaptic transmission, the communication of a signal from one neuron to the next, is abnormally increased or decreased. The changes in synaptic transmission after injury may occur through mechanisms of normal plasticity that underlie learning a new task or acquiring a foreign language. Alternatively, they may involve completely unique mechanisms. Our goal is to determine the cellular mechanisms of injury-induced plasticity of synaptic transmission. This is a Herculean task in the complex environment of the spinal cord or brain, where thousands of neurons make millions of synapses with each other. We simplify the problem by looking at the effects of injury on one synapse, the synapse between the motor neuron and the muscle, the neuromuscular junction. To mimic the effects of injury, we block all activity at the neuromuscular junction with tetrodotoxin, the toxin of puffer fish that can kill a person by paralyzing the diaphragm. Our data suggest that the synaptic vesicle protein RabSA is essential for injury-induced plasticity. To test this hypothesis, we will determine how injury-induced plasticity is altered in a mutant mouse with impaired RabSA function. The studies in this proposal will significantly advance our understanding of the nervous system's response to long term changes in activity that occur after injury. Such knowledge is essential in the fight to prevent long term disabilities.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Program Projects (P01)
Project #
5P01NS057228-05
Application #
8321019
Study Section
National Institute of Neurological Disorders and Stroke Initial Review Group (NSD)
Project Start
Project End
2013-02-28
Budget Start
2011-09-01
Budget End
2013-08-31
Support Year
5
Fiscal Year
2011
Total Cost
$173,959
Indirect Cost
Name
Wright State University
Department
Type
DUNS #
047814256
City
Dayton
State
OH
Country
United States
Zip Code
45435
Wang, Xueyong; McIntosh, J Michael; Rich, Mark M (2018) Muscle Nicotinic Acetylcholine Receptors May Mediate Trans-Synaptic Signaling at the Mouse Neuromuscular Junction. J Neurosci 38:1725-1736
Wang, Xueyong; Rich, Mark M (2018) Homeostatic synaptic plasticity at the neuromuscular junction in myasthenia gravis. Ann N Y Acad Sci 1412:170-177
Schultz, Adam J; Rotterman, Travis M; Dwarakanath, Anirudh et al. (2017) VGLUT1 synapses and P-boutons on regenerating motoneurons after nerve crush. J Comp Neurol 525:2876-2889
Wang, Xueyong; Pinter, Martin J; Rich, Mark M (2016) Reversible Recruitment of a Homeostatic Reserve Pool of Synaptic Vesicles Underlies Rapid Homeostatic Plasticity of Quantal Content. J Neurosci 36:828-36
Vincent, Jacob A; Wieczerzak, Krystyna B; Gabriel, Hanna M et al. (2016) A novel path to chronic proprioceptive disability with oxaliplatin: Distortion of sensory encoding. Neurobiol Dis 95:54-65
Romer, Shannon H; Deardorff, Adam S; Fyffe, Robert E W (2016) Activity-dependent redistribution of Kv2.1 ion channels on rat spinal motoneurons. Physiol Rep 4:
Smilde, Hiltsje A; Vincent, Jake A; Baan, Guus C et al. (2016) Changes in muscle spindle firing in response to length changes of neighboring muscles. J Neurophysiol 115:3146-55
McGovern, Vicki L; Massoni-Laporte, Aurélie; Wang, Xueyong et al. (2015) Plastin 3 Expression Does Not Modify Spinal Muscular Atrophy Severity in the ?7 SMA Mouse. PLoS One 10:e0132364
Vincent, Jacob A; Nardelli, Paul; Gabriel, Hanna M et al. (2015) Complex impairment of IA muscle proprioceptors following traumatic or neurotoxic injury. J Anat 227:221-30
Romer, Shannon H; Dominguez, Kathleen M; Gelpi, Marc W et al. (2014) Redistribution of Kv2.1 ion channels on spinal motoneurons following peripheral nerve injury. Brain Res 1547:1-15

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