Classifying visual system cells and studying their microcircuitry is essential to understanding the neural networks which underlie visual processes. Our laboratory identifies specific cell classes and synapses and traces their curcuitry in the visual system in order to study the structural correlates of cell physiology. We use a variety of research techniques, including neurotransmitter labeling, filling of cells and axons with horseradish peroxidase conjugated wheat germ agglutinin, computerized morphometry, and 3-D serial section reconstruction. Using these approaches, we have recently identified four types of relay cell and two classes of gamma - aminobutyric acid accumulating cell in the superior colliculus. We have also found distinctive synaptic relationships of retinal synapses in different visual structures. During the proposed grant period, we want to study the relay cells and interneurons of the superior colliculus and lateral geniculate nucleus. Cells and processes will be marked by retrograde filling with HRP-conjugated wheat germ agglutinin (WGA). The density and spatial distribution of synapses on these cells from the retina, visual cortex, and tegmentum will be studied from serial section reconstructions. We will also examine the cell's size, cytology, and dendritic geometry using computerized morphometry. The putative neurotransmitters of these cells and synapses will also be studied. We will look for the accumulation of radiolabeled glutamate, glycine, gamma-aminobutyric acid, choline, b-alanine, and taurine using electron microscope autoradiography after in vivo injection or in vitro incubation. We will localize putative cholinergic receptor sites using radiolabeled alpha-bungarotoxin. Serotonin and two peptides will be localized using antibody immunohistochemistry. The results will allow us to classify cell types in the superior colliculus and lateral geniculate nucleus based upon a parametric analysis of their morphology, synaptic patterns, and accumulation of neurotransmitters and to determine the synaptic interconnections with underlie the functional circuits of these two visual structures.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
5R01EY002973-06
Application #
3257284
Study Section
Visual Sciences B Study Section (VISB)
Project Start
1979-08-01
Project End
1986-12-31
Budget Start
1986-01-01
Budget End
1986-12-31
Support Year
6
Fiscal Year
1986
Total Cost
Indirect Cost
Name
University of Tennessee Health Science Center
Department
Type
Schools of Medicine
DUNS #
941884009
City
Memphis
State
TN
Country
United States
Zip Code
38163
Lo, Fu-Sun; Mize, R Ranney (2002) Properties of LTD and LTP of retinocollicular synaptic transmission in the developing rat superior colliculus. Eur J Neurosci 15:1421-32
Mize, R Ranney; Graham, Sean K; Cork, R John (2002) Expression of the L-type calcium channel in the developing mouse visual system by use of immunocytochemistry. Brain Res Dev Brain Res 136:185-95
Scheiner, C A; Kratz, K E; Guido, W et al. (2001) Prenatal and postnatal expression of nitric oxide in the developing kitten superior colliculus revealed with NADPH diaphorase histochemistry. Vis Neurosci 18:43-54
Lo, F S; Mize, R R (2000) Synaptic regulation of L-type Ca(2+) channel activity and long-term depression during refinement of the retinocollicular pathway in developing rodent superior colliculus. J Neurosci 20:RC58
Mize, R R; Butler, G D (2000) The NMDAR1 subunit of the N-methyl-D-aspartate receptor is localized at postsynaptic sites opposite both retinal and cortical terminals in the cat superior colliculus. Vis Neurosci 17:41-53
Wu, H H; Cork, R J; Huang, P L et al. (2000) Refinement of the ipsilateral retinocollicular projection is disrupted in double endothelial and neuronal nitric oxide synthase gene knockout mice. Brain Res Dev Brain Res 120:105-11
Mize, R R; Lo, F (2000) Nitric oxide, impulse activity, and neurotrophins in visual system development(1). Brain Res 886:15-32
Wu, H H; Cork, R J; Mize, R R (2000) Normal development of the ipsilateral retinocollicular pathway and its disruption in double endothelial and neuronal nitric oxide synthase gene knockout mice. J Comp Neurol 426:651-65
Cork, R J; Calhoun, T; Perrone, M et al. (2000) Postnatal development of nitric oxide synthase expression in the mouse superior colliculus. J Comp Neurol 427:581-92
Scheiner, C A; Cork, R J; Mize, R R (1999) Failure to disrupt development of cholinergic fiber patches in the superior colliculus in nitric oxide synthase deficient mice. Brain Res Dev Brain Res 118:217-20

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