Gap junctions are microscopic connections that for four decades have been known to provide for direct intercellular and metabolic coupling between nerve cells in the brain, retina and spinal cord. Previously, gap junctions between neurons were thought to be large but rare, and only between a few types of non-cognitive neurons and only in limited areas of the central nervous system. The discovery of """"""""mini"""""""" gap junctions and preliminary evidence for their possible abundance throughout the brain suggests that """"""""mini"""""""" gap junctions may provide the structural basis for propagation of tiny """"""""sub threshold electrical spikelets"""""""" or """"""""partial spikes"""""""" in primary neurons throughout the brain. We propose to use newly developed high-resolution immunocytochemical methods [both laser scanning confocal immunofluorescence microscopy and freezefracture replica immunogold labeling (FRIL) electron microscopy] to detect, quantify, determine the protein composition of, and measure the sizes of all classes of gap junctions throughout the brain of mice and to make detailed measurements of """"""""mini"""""""" gap junctions in selected regions of human brain. We will emphasize analysis of those regions that are primarily responsible for thinking and consciousness, learning and memory, and fine motor control (i.e., cerebral cortex, hippocampus, cerebellum, and inferior olive). These data are essential to the understanding of how consciousness is created, how a person awakes from sleep and general anesthesia, how memories are created, how fine motor control is created or lost during disabling diseases such as Parkinsonism, as well as for development of drugs to treat disorders of each of these processes.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
High Priority, Short Term Project Award (R56)
Project #
2R56NS044395-06
Application #
7441321
Study Section
Biophysics of Neural Systems Study Section (BPNS)
Program Officer
Silberberg, Shai D
Project Start
2002-07-01
Project End
2008-05-31
Budget Start
2007-08-01
Budget End
2008-05-31
Support Year
6
Fiscal Year
2007
Total Cost
$359,750
Indirect Cost
Name
Colorado State University-Fort Collins
Department
Microbiology/Immun/Virology
Type
Schools of Veterinary Medicine
DUNS #
785979618
City
Fort Collins
State
CO
Country
United States
Zip Code
80523
Nagy, James I; Pereda, Alberto E; Rash, John E (2018) Electrical synapses in mammalian CNS: Past eras, present focus and future directions. Biochim Biophys Acta Biomembr 1860:102-123
Wang, S G; Tsao, D D; Vanderpool, K G et al. (2017) Connexin36 localization to pinealocytes in the pineal gland of mouse and rat. Eur J Neurosci 45:1594-1605
Rash, J E; Kamasawa, N; Vanderpool, K G et al. (2015) Heterotypic gap junctions at glutamatergic mixed synapses are abundant in goldfish brain. Neuroscience 285:166-93
Yao, Cong; Vanderpool, Kimberly G; Delfiner, Matthew et al. (2014) Electrical synaptic transmission in developing zebrafish: properties and molecular composition of gap junctions at a central auditory synapse. J Neurophysiol 112:2102-13
Bautista, W; Rash, J E; Vanderpool, K G et al. (2014) Re-evaluation of connexins associated with motoneurons in rodent spinal cord, sexually dimorphic motor nuclei and trigeminal motor nucleus. Eur J Neurosci 39:757-70
Serrano-Velez, Jose L; Rodriguez-Alvarado, Melanie; Torres-Vazquez, Irma I et al. (2014) Abundance of gap junctions at glutamatergic mixed synapses in adult Mosquitofish spinal cord neurons. Front Neural Circuits 8:66
Bautista, W; Nagy, J I (2014) Connexin36 in gap junctions forming electrical synapses between motoneurons in sexually dimorphic motor nuclei in spinal cord of rat and mouse. Eur J Neurosci 39:771-87
Rash, John E; Curti, Sebastian; Vanderpool, Kimberly G et al. (2013) Molecular and functional asymmetry at a vertebrate electrical synapse. Neuron 79:957-69
Nagy, J I; Bautista, W; Blakley, B et al. (2013) Morphologically mixed chemical-electrical synapses formed by primary afferents in rodent vestibular nuclei as revealed by immunofluorescence detection of connexin36 and vesicular glutamate transporter-1. Neuroscience 252:468-88
Curti, Sebastian; Hoge, Gregory; Nagy, James I et al. (2012) Synergy between electrical coupling and membrane properties promotes strong synchronization of neurons of the mesencephalic trigeminal nucleus. J Neurosci 32:4341-59

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