Regulation of Capillary Blood Flow in the Choroid Vasculature
About the Research Project
Program
Award Type
New Investigator Grant
Award Amount
$446,943
Active Dates
July 01, 2022 - June 30, 2025
Grant ID
M2022010N
Goals
The goal of the project is to understand the non-neuronal mechanisms regulating choroidal blood flow and identify new therapeutic targets relating to the pathogenesis of age-related macular degeneration.
Summary
Using high-speed and high-resolution spinning disk microscopy and a novel ex vivo pressurized-choroidal vasculature preparation, we will examine how the application of light affects the contractile state of the blood vessels controlling choroidal blood flow. In addition, we will employ a combination of molecular biology, patch-clamp electrophysiology, and super-resolution imaging to identify the cellular targets and ion channels responsible for the light-dependent constriction of choroidal blood vessels.
Unique and Innovative
The current proposal will use a combination of novel approaches to test the hypothesis that light stimulates light and can affect endothelial cell and mural cell calcium dynamics leading to changes in vascular tone. These approaches include a novel ex vivo pressurized-vasculature preparation; new transgenic mice expressing fluorescent calcium biosensors; and choroidal tissue from Cynomolgus monkeys. Conceptual innovations include the concept that K+ efflux is a cellular signaling modality acting on the choriocapillaris as sensory webs responding to the metabolic needs of nearby photoreceptors.
Foreseeable Benefits
Successful completion of the current proposal will transform our understanding of the function of capillary networks within the choroidal vasculature, establishing these networks as sensors and active contributors to the regulation of local blood flow necessary to meet the unique metabolic demand of photoreceptors of the eye. By building a better understanding of the non-neuronal mechanisms of blood flow control, the proposed work will provide new insights into the pathogenesis of age-related macular degeneration and unearth new pathophysiological targets for therapeutic interventions.
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