The long term objective of this research program is to characterize the ion conductance properties of Muller cell membrane and to determine the role that Muller cells play in electroretinogram (ERG) generation and in the regulation of extracellular K+ levels in the retina. Studies conducted during the previous grant period demonstrated that the amphibian Muller cell membrane is almost exclusively permeable to K+ and that 84 to 95% of total Muller cell conductance is located in the endfoot process of the cell.
Specific aims for the forthcoming grant period include the following: 1) Determine whether the Muller cell endfeet of mammals have high K+ conductance properties similar to those of amphibians. 2) Localize precisely and determine the specific membrane conductance of the high K+ conductance region of the Muller cell endfoot. 3) Investigate the recently discovered voltage-sensitive conductance properties of the Muller cell membrane. 4) Determine the pharmacological properties of Muller cell K+ channels. 5) Determine whether the endfeet of mammalian retinal astrocytes have high K+ conductance. 6) Conduct direct experimental tests to determine whether Muller cells generate components of the ERG and contribute to the regulation of K+ levels within the retina. 7) Study Muller cell function using computer simulations of K+ dynamics and current generation in the retina. Muller cell membrane properties and function will be studied in dissociated cell, retinal slice and eyecup preparations of amphibian and mammalian species using intracellular, patch-clamp and ion-selective microelectrode recording techniques. The studies outlined in this proposal will clarify the role that Muller cells play in the generation of the ERG, which is an important clinical tool used in diagnosing many retinal disorders including diabetic retinopathy and retinitis pigmentosa. These studies will also elucidate the role that Muller cells play in regulating K+ levels within the retina. Disruption of such regulation may be related to pathological retinal conditions.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
5R01EY004077-06
Application #
3258559
Study Section
Visual Sciences A Study Section (VISA)
Project Start
1982-04-01
Project End
1990-03-31
Budget Start
1987-04-01
Budget End
1988-03-31
Support Year
6
Fiscal Year
1987
Total Cost
Indirect Cost
Name
Schepens Eye Research Institute
Department
Type
DUNS #
City
Boston
State
MA
Country
United States
Zip Code
02114
Nippert, Amy R; Biesecker, Kyle R; Newman, Eric A (2018) Mechanisms Mediating Functional Hyperemia in the Brain. Neuroscientist 24:73-83
Srienc, Anja I; Biesecker, Kyle R; Shimoda, Angela M et al. (2016) Ischemia-induced spreading depolarization in the retina. J Cereb Blood Flow Metab 36:1579-91
Biesecker, Kyle R; Srienc, Anja I; Shimoda, Angela M et al. (2016) Glial Cell Calcium Signaling Mediates Capillary Regulation of Blood Flow in the Retina. J Neurosci 36:9435-45
Kornfield, Tess E; Newman, Eric A (2015) Measurement of Retinal Blood Flow Using Fluorescently Labeled Red Blood Cells. eNeuro 2:
Newman, Eric A (2015) Glial cell regulation of neuronal activity and blood flow in the retina by release of gliotransmitters. Philos Trans R Soc Lond B Biol Sci 370:
MacVicar, Brian A; Newman, Eric A (2015) Astrocyte regulation of blood flow in the brain. Cold Spring Harb Perspect Biol 7:
Kur, Joanna; Newman, Eric A (2014) Purinergic control of vascular tone in the retina. J Physiol 592:491-504
Kornfield, Tess E; Newman, Eric A (2014) Regulation of blood flow in the retinal trilaminar vascular network. J Neurosci 34:11504-13
Newman, Eric A (2013) Functional hyperemia and mechanisms of neurovascular coupling in the retinal vasculature. J Cereb Blood Flow Metab 33:1685-95
Kur, Joanna; Newman, Eric A; Chan-Ling, Tailoi (2012) Cellular and physiological mechanisms underlying blood flow regulation in the retina and choroid in health and disease. Prog Retin Eye Res 31:377-406

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