How visual information is processed and transformed in the nervous system is a fundamental question in vision research. Given its clear importance in visually-guided behaviors and the available genetic tools, the mouse superior colliculus (SC) holds great promise for understanding visual processing and its neural mechanisms. The SC is a midbrain structure important for multimodal integration and sensorimotor transformation. Its superficial layers are purely visual and receive direct inputs from the retina. In this proposal, the investigators will study motion processing in a visual layer of the SC, the SGS, with a particular focus on its modulation by stimulus context, locomotion state, and self-generated visual flow. First, in vivo whole cell recording will be performed to determine the synaptic inputs that individual SGS neurons receive from the region surrounding their receptive fields. These experiments will reveal the local connectivity of excitatory and inhibitory neurons that mediates the bidirectional encoding of motion contrast between the visual stimulus and its context. Second, two-photon calcium imaging will be performed in awake mice to determine whether and how locomotion affects visual responses in the SGS. These experiments will be done across the depth of the SGS and in a cell- type-specific manner. Finally, the investigators will study whether and how self-generated visual flow affects the responses of SGS neurons. Two-photon imaging and physiological recording will be performed in head- restrained mice running in a virtual reality system. These experiments will be conducted across different retinotopic locations in the SGS, in order to reveal whether a region-specific organization exists in the SGS in the context of encoding self-generated motion. Together, these experiments will generate important data needed for a complete understanding of visual processing in the brain. Because normal visual processing is compromised in a number of neurological and psychiatric disorders, such as dyslexia, schizophrenia, and autism spectrum disorders, these studies will provide novel insights for the understanding and treatment of these disorders.

Public Health Relevance

A long-term goal of our research is to reveal the brain circuitry and synaptic mechanisms of visual signal processing and transformation. Because normal visual processing is compromised in a number of neurological and psychiatric disorders, such as dyslexia, schizophrenia and autism spectrum disorders, our studies will provide important insights for the understanding and treatment of these disorders.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
2R01EY026286-05
Application #
10052106
Study Section
Mechanisms of Sensory, Perceptual, and Cognitive Processes Study Section (SPC)
Program Officer
Flanders, Martha C
Project Start
2015-12-01
Project End
2023-08-31
Budget Start
2020-09-01
Budget End
2021-08-31
Support Year
5
Fiscal Year
2020
Total Cost
Indirect Cost
Name
University of Virginia
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
065391526
City
Charlottesville
State
VA
Country
United States
Zip Code
22904
Shi, Xuefeng; Jin, Yanjiao; Cang, Jianhua (2018) Transformation of Feature Selectivity From Membrane Potential to Spikes in the Mouse Superior Colliculus. Front Cell Neurosci 12:163
Barchini, Jad; Shi, Xuefeng; Chen, Hui et al. (2018) Bidirectional encoding of motion contrast in the mouse superior colliculus. Elife 7:
Liu, Pan; Thomson, Benjamin R; Khalatyan, Natalia et al. (2018) Selective permeability of mouse blood-aqueous barrier as determined by 15N-heavy isotope tracing and mass spectrometry. Proc Natl Acad Sci U S A 115:9032-9037
Cang, Jianhua; Savier, Elise; Barchini, Jad et al. (2018) Visual Function, Organization, and Development of the Mouse Superior Colliculus. Annu Rev Vis Sci 4:239-262
Shi, Xuefeng; Barchini, Jad; Ledesma, Hector Acaron et al. (2017) Retinal origin of direction selectivity in the superior colliculus. Nat Neurosci 20:550-558
Feng, Liang; Puyang, Zhen; Chen, Hui et al. (2017) Overexpression of Brain-Derived Neurotrophic Factor Protects Large Retinal Ganglion Cells After Optic Nerve Crush in Mice. eNeuro 4:
Puyang, Zhen; Gong, Hai-Qing; He, Shi-Gang et al. (2017) Different functional susceptibilities of mouse retinal ganglion cell subtypes to optic nerve crush injury. Exp Eye Res 162:97-103
Levine, Jared N; Chen, Hui; Gu, Yu et al. (2017) Environmental Enrichment Rescues Binocular Matching of Orientation Preference in the Mouse Visual Cortex. J Neurosci 37:5822-5833
Feng, Liang; Chen, Hui; Yi, Ji et al. (2016) Long-Term Protection of Retinal Ganglion Cells and Visual Function by Brain-Derived Neurotrophic Factor in Mice With Ocular Hypertension. Invest Ophthalmol Vis Sci 57:3793-802
Yi, Ji; Puyang, Zhen; Feng, Liang et al. (2016) Optical Detection of Early Damage in Retinal Ganglion Cells in a Mouse Model of Partial Optic Nerve Crush Injury. Invest Ophthalmol Vis Sci 57:5665-5671

Showing the most recent 10 out of 11 publications