Visual processing is mediated by precise neural connections organized in a hybrid parallel and heirarchical architecture. Parallel magno (M)- and parvocellular (P) streams are segregated in early visual pathways, and provide input to separate populations of neurons in primary visual cortex (V1). Within V1, however, information from these two pathways is integrated to give rise to output neurons influenced by both. The proposed work is aimed at obtaining a detailed understanding of the circuits mediating these interactions. What are the relationships between the M and P pathways and the neurons that project from V1 to higher , extrastriate visual cortical areas? The flow of information will be studied within V1, from layers 4Calpha and 4Cbeta (which receive M and P input respectively) to 3 major populations of extrastriate projection neurons in layer 4B, layer 2/3 """"""""blobs , layer 2/3 interblobs . These studies will also assess the extent of interactions between neurons in blobs and the specificity of these horizontal"""""""" connections for ocular dominance columns. All of the studies will utilize intracellular labeling of individual neurons with biocytin during whole- cell recording in living slices of V1. Subsequent anatomical reconstructions will identify the locations of their synapses. In particular, the positions of synaptic boutons from individual layer 4B will be determined. Similar measures will reveal the specificity of horizontal connections from layer 2/3 neurons. Understanding the mechanisms mediating normal visual perception is crucial to identifying processing defects in human patients suffering from strabismus and amblyiopia. These studies may also shed light on causes of dyslexia, which is linked to deficits related to the M pathway.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
1F32EY006837-01
Application #
2420030
Study Section
Visual Sciences B Study Section (VISB)
Project Start
1999-01-01
Project End
Budget Start
1998-07-01
Budget End
1999-06-30
Support Year
1
Fiscal Year
1998
Total Cost
Indirect Cost
Name
Salk Institute for Biological Studies
Department
Type
DUNS #
005436803
City
La Jolla
State
CA
Country
United States
Zip Code
92037
Yue, Wendy Wing Sze; Frederiksen, Rikard; Ren, Xiaozhi et al. (2017) Spontaneous activation of visual pigments in relation to openness/closedness of chromophore-binding pocket. Elife 6:
Liao, Hsi-Wen; Ren, Xiaozhi; Peterson, Beth B et al. (2016) Melanopsin-expressing ganglion cells on macaque and human retinas form two morphologically distinct populations. J Comp Neurol 524:2845-72
Zhang, Tao; Cao, Li-Hui; Kumar, Sandeep et al. (2016) Dimerization of visual pigments in vivo. Proc Natl Acad Sci U S A 113:9093-8
Sun, Lu O; Jiang, Zheng; Rivlin-Etzion, Michal et al. (2013) On and off retinal circuit assembly by divergent molecular mechanisms. Science 342:1241974
Pearson, R A; Barber, A C; Rizzi, M et al. (2012) Restoration of vision after transplantation of photoreceptors. Nature 485:99-103
Matsuoka, Ryota L; Jiang, Zheng; Samuels, Ivy S et al. (2012) Guidance-cue control of horizontal cell morphology, lamination, and synapse formation in the mammalian outer retina. J Neurosci 32:6859-68
Sakai, Kazumi; Imamoto, Yasushi; Su, Chih-Ying et al. (2012) Photochemical nature of parietopsin. Biochemistry 51:1933-41
Fan, Jie; Sakurai, Keisuke; Chen, Ching-Kang et al. (2010) Deletion of GRK1 causes retina degeneration through a transducin-independent mechanism. J Neurosci 30:2496-503