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Completed NON-SBIR/STTR RPGS NIH (US)

Structure and Function of Primate Retinal Circuits

$3.89M USD

Funder NATIONAL EYE INSTITUTE
Recipient Organization University of California Berkeley
Country United States
Start Date Jan 01, 2021
End Date Nov 30, 2025
Duration 1,794 days
Number of Grantees 1
Roles Principal Investigator
Data Source NIH (US)
Grant ID 10747341
Grant Description

An understanding of the normal structure and function of the retina is important to appreciate changes that occur during disease, development and aging. To this end, a longstanding goal for the field has been to obtain a unified functional, molecular and morphological classification of the neural cell types in

the primate retina. To address this need, we will use a state-of-the-art approach to interrogate neuronal function in molecularly-defined ganglion and amacrine cell types in primate retina. Our method combines two-photon calcium imaging of light-evoked responses with a novel, high-throughput method to molecularly classify cell types in situ and at unprecedented scale. We will use this integrated

approach to determine the functional properties of molecularly-defined wide-field ganglion cells and GABAergic amacrine cell types that have hitherto been difficult to target using conventional electrophysiological approaches. In Aim 1, we will determine the spatiotemporal response properties, mosaics and morphologies of ganglion cell types that are disproportionately represented in peripheral

retina. In Aim 2, we will examine how regional differences in inhibitory neurons and their connections shape the functional response properties of the foveal and peripheral retina. We expect that completion of these aims will reveal novel insights into the distinct cellular and circuit mechanisms that shape

visual processing in the foveal and peripheral retina.

All Grantees

University of California Berkeley

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