This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. This research project is concerned with the functional organization and information processing of the second visual area (V2). Area V2 neurons are known to process elemental aspects of the visual scene such as stimulus orientation, color and depth, and are thought to participate in the combination of visual information that is processed independently by other neurons. Histology has revealed repeated cycles of ?thin?, ?pale? and ?thick ? stripe compartments across Area V2, and there is a reported tendency for different neural response characteristics in each stripe class (e.g., color-preferring in thin stripe, cf. orientation-preferring in pale and thick stripes). In this project we will investigate the functional role of marginal zones of the thin and pale stripes in the processing of color and orientation. Intrinsic optical imaging methods will map the collective response preference of neurons at sub-millimeter scale, and functionally define the thin/pale marginal zones. Based on this map, single neurons will be selected for comprehensive electrophysiological characterization. By combining functional mapping methods with single neuron electrophysiology we aim to identify unique neuronal properties and mechanisms (such as combinatorial coding and selectivity maintenance) associated with these neural locales in Area V2. These experiments, in particular, are intended to improve understanding of the basic mechanisms associated with cortical visual processing. However, in general, they also seek to reveal fundamental relationships between single neuron response and the collective response of the surrounding neural environment. Understanding this relationship is important because many brain measurement techniques can only record neural responses at the collective rather than single neuron scale. Knowledge of this relationship will aid understanding of the neural basis of imaged brain function, and guide future brain data interpretation.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Exploratory Grants (P20)
Project #
5P20RR015574-07
Application #
7381125
Study Section
Special Emphasis Panel (ZRR1-RI-8 (02))
Project Start
2006-05-01
Project End
2007-04-30
Budget Start
2006-05-01
Budget End
2007-04-30
Support Year
7
Fiscal Year
2006
Total Cost
$225,607
Indirect Cost
Name
West Virginia University
Department
Otolaryngology
Type
Schools of Medicine
DUNS #
191510239
City
Morgantown
State
WV
Country
United States
Zip Code
26506
Rodgers, H M; Huffman, V J; Voronina, V A et al. (2018) The role of the Rx homeobox gene in retinal progenitor proliferation and cell fate specification. Mech Dev 151:18-29
Khawaja, Anthony P; Cooke Bailey, Jessica N; Wareham, Nicholas J et al. (2018) Genome-wide analyses identify 68 new loci associated with intraocular pressure and improve risk prediction for primary open-angle glaucoma. Nat Genet 50:778-782
Lewis, James W; Silberman, Magenta J; Donai, Jeremy J et al. (2018) Hearing and orally mimicking different acoustic-semantic categories of natural sound engage distinct left hemisphere cortical regions. Brain Lang 183:64-78
Brefczynski-Lewis, Julie A; Lewis, James W (2017) Auditory object perception: A neurobiological model and prospective review. Neuropsychologia 105:223-242
Pasquale, Louis R (2016) Vascular and autonomic dysregulation in primary open-angle glaucoma. Curr Opin Ophthalmol 27:94-101
Rodgers, Helen M; Belcastro, Marycharmain; Sokolov, Maxim et al. (2016) Embryonic markers of cone differentiation. Mol Vis 22:1455-1467
Li, Zheng; Allingham, R Rand; Nakano, Masakazu et al. (2015) A common variant near TGFBR3 is associated with primary open angle glaucoma. Hum Mol Genet 24:3880-92
Springelkamp, Henriët; Höhn, René; Mishra, Aniket et al. (2014) Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process. Nat Commun 5:4883
Loomis, Stephanie J; Kang, Jae H; Weinreb, Robert N et al. (2014) Association of CAV1/CAV2 genomic variants with primary open-angle glaucoma overall and by gender and pattern of visual field loss. Ophthalmology 121:508-16
Ozel, A Bilge; Moroi, Sayoko E; Reed, David M et al. (2014) Genome-wide association study and meta-analysis of intraocular pressure. Hum Genet 133:41-57

Showing the most recent 10 out of 63 publications