Orientation selectivity in the population of ON-OFF direction-selective ganglion cells in the mouse retina
dc.contributor.author | Ravi Chander, Prathyusha | |
dc.contributor.supervisor | Awatramani, Gautam | |
dc.date.accessioned | 2023-04-28T16:37:19Z | |
dc.date.copyright | 2023 | en_US |
dc.date.issued | 2023-04-28 | |
dc.degree.department | Department of Biology | en_US |
dc.degree.level | Master of Science M.Sc. | en_US |
dc.description.abstract | In the mammalian retina, the orientation-selective (OS) and direction-selective (DS) information are generally thought to be relayed to higher visual centers via distinct ganglion cell types. Contrary to this notion, here I report that classic ON-OFF direction-selective ganglion cells (DSGCs) that are known to encode the four cardinal directions, also encode orientation of static stimuli. The DSGC’s preferred orientations was always orthogonal to its preferred-null axis defined by moving stimuli. To evaluate the synaptic mechanisms underlying orientation selectivity a combination of electrophysiological, optogenetic, and gene knock-out techniques were used to assess the functional properties of all four types of ON-OFF DSGCs. Cumulative results from multiple approaches revealed that the glutamate input to all four types of DSGCs was tuned to the vertical axis. This relies on signals from a specific presynaptic source (the bipolar cell type 5A; BC5A), which appear to be electrically coupled to vertically oriented processes of wide-field amacrine cells. By contrast, the GABAergic inhibition mediated largely by starburst amacrine cells was tuned either along the horizontal or vertical axis, consistent with their well-defined asymmetric wiring pattern. Thus, distinct combinations of inhibition and excitation underlie orientation selectivity in the nasal/temporal and dorsal/ventral coding DSGC populations, only the latter critically relying on the starbursts. Together, my work provides novel insights into how feature selectivity emerges in the hierarchical network in the retina. | en_US |
dc.description.scholarlevel | Graduate | en_US |
dc.identifier.uri | http://hdl.handle.net/1828/15044 | |
dc.language | English | eng |
dc.language.iso | en | en_US |
dc.rights | Available to the World Wide Web | en_US |
dc.subject | Direction-selective | en_US |
dc.subject | Orientation-selective | en_US |
dc.subject | Electrophysiology | en_US |
dc.subject | Optogenetics | en_US |
dc.subject | Asymmetric inhibition | en_US |
dc.subject | Vertical excitation | en_US |
dc.subject | OS is orthogonal to the P-N axis | en_US |
dc.subject | dv-DSGCs | en_US |
dc.subject | nt-DSGCs | en_US |
dc.subject | SACs | en_US |
dc.subject | BC5As | en_US |
dc.subject | WACs | en_US |
dc.subject | Gap-junction coupling | en_US |
dc.subject | Cx36 gap-junctions | en_US |
dc.subject | Genetic knockout | en_US |
dc.title | Orientation selectivity in the population of ON-OFF direction-selective ganglion cells in the mouse retina | en_US |
dc.type | Thesis | en_US |
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