Higher visual functions, including object recognition and global motion detection, are carried out by extrastriate visual areas, or higher visual areas (HVAs), downstream from primary visual cortex. These higher processing functions often fail to completely recover following congenital blindness or amblyopia. These observations suggest that early visual experience sculpts HVA circuitry, but this has not been determined. To address this gap in knowledge, we propose an integrative approach using genetically engineered mice. Our goal is to determine how experience sculpts the normal development of HVA circuitry and how circuit deficits are caused by visual deprivation. Our preliminary data indicates that a subset of HVAs is slow to develop after eye opening, and fails to completely recover visual responses following dark rearing. By contrast, a complementary set of HVAs is visually responsive at eye opening, and fully recovers following dark rearing. We will map the development of HVAs at multiple time points, starting at eye opening, using intrinsic signal optical imaging and two photon calcium imaging. We will use a paradigm we developed for high resolution receptive field mapping of local populations of neurons in parallel. We will use technology we have recently developed to examine activity correlations between visual cortical areas and map how these change in development. We will dark rear mice to determine the effect of visual deprivation on HVA circuitry. The results from this project will reveal the role of visual experience in sculpting HVA selectivity and circuit development.
Many disorders of brain function, including higher visual processing deficits following early blindness, result from altered development of cortical circuitr beyond primary sensory and motor areas. However, we know little about the experience-dependent development of these higher cortical areas. The proposed studies will provide a definitive account of the development of higher visual areas in the mouse, and the consequences of deprived sensory experience on the development of this circuitry.
Yu, Yiyi; Hira, Riichiro; Stirman, Jeffrey N et al. (2018) Mice use robust and common strategies to discriminate natural scenes. Sci Rep 8:1379 |
Townsend, Leah B; Smith, Spencer L (2017) Genotype- and sex-dependent effects of altered Cntnap2 expression on the function of visual cortical areas. J Neurodev Disord 9:2 |
Smith, Ikuko T; Townsend, Leah B; Huh, Ruth et al. (2017) Stream-dependent development of higher visual cortical areas. Nat Neurosci 20:200-208 |
Nakamura, Ayumi; Swahari, Vijay; Plestant, Charlotte et al. (2016) Bcl-xL Is Essential for the Survival and Function of Differentiated Neurons in the Cortex That Control Complex Behaviors. J Neurosci 36:5448-61 |
Stirman, Jeffrey N; Smith, Ikuko T; Kudenov, Michael W et al. (2016) Wide field-of-view, multi-region, two-photon imaging of neuronal activity in the mammalian brain. Nat Biotechnol 34:857-62 |
Stirman, Jeffrey; Townsend, Leah B; Smith, Spencer (2016) A touchscreen based global motion perception task for mice. Vision Res 127:74-83 |
Kim, Hyojin; Kunz, Portia A; Mooney, Richard et al. (2016) Maternal Loss of Ube3a Impairs Experience-Driven Dendritic Spine Maintenance in the Developing Visual Cortex. J Neurosci 36:4888-94 |
Ji, Na; Freeman, Jeremy; Smith, Spencer L (2016) Technologies for imaging neural activity in large volumes. Nat Neurosci 19:1154-64 |
Harris, Kenneth D; Quiroga, Rodrigo Quian; Freeman, Jeremy et al. (2016) Improving data quality in neuronal population recordings. Nat Neurosci 19:1165-74 |