Photoreceptors and bipolar cells of the retina and hair cells of the auditory and vestibular systems signal sensory stimuli as graded changes in neurotransmitter release. To do so, these cells have evolved synaptic ribbons, proteinaceous structures that tether large numbers of synaptic vesicles near release sites. The molecular machinery underlying synaptic ribbon function is poorly understood. A handful of proteins have been localized to the synaptic ribbon and the importance of these individual molecules as well as how they contribute to the unique functions of the synaptic ribbon remains elusive. Of these proteins, the most abundant is Ribeye, a protein unique to the synaptic ribbon and thought to constitute most of the synaptic ribbon and hypothesized to form the core of the synaptic ribbon. Ribeye arises from an alternative start site of the transcriptional corepressor CtBP2. The precise role of Ribeye remains unknown and the long-term goal of this proposal is to determine the functional role of Ribeye in the synaptic ribbon. To study Ribeye function, we will employ a combination of molecular biology, genetic and electrophysiology primarily using zebrafish as a primary model system.
In Aim 1 we generated and characterize zebrafish with targeted mutations in both ribeye genes.
In Aim 2, we the effect of one or both Ribeye gene products on the structure of photoreceptor and hair cell ribbons.
In Aim 3, we will look at the effect of Ribey removal on the distribution and localization of other synaptic ribbon proteins.
In Aim 4, we will investigate the effects of Ribeye loss on exocytosis and calcium current in neuromast hair cells. Understanding synaptic ribbon function at the molecular level will ultimately aid in understanding how visual and auditory information is processed and communicated. In addition, it may provide clues to help understand diseases that specifically affect vision and hearing. In addition, the fundamental understanding of presynaptic processes in these specialized neurons will have broader implications for neuronal communication in general and thus, may contribute to our understanding of various aspects of mental health and neurological disorders.

Public Health Relevance

In the retina and inner ear, primary sensory information is transmitted at specialized synapses specially evolved to transmit high rates of neurotransmitter release in a graded manner. We aim to understand, at the molecular level, how these cells accomplish this task. Understanding these synapses will ultimately aid in understanding how visual and auditory information is processed and communicated and provide clues to help understand diseases that specifically affect vision and hearing.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
5R01EY021195-06
Application #
9316630
Study Section
Neurotransporters, Receptors, and Calcium Signaling Study Section (NTRC)
Program Officer
Greenwell, Thomas
Project Start
2011-08-01
Project End
2020-07-31
Budget Start
2017-08-01
Budget End
2018-07-31
Support Year
6
Fiscal Year
2017
Total Cost
Indirect Cost
Name
Yale University
Department
Physiology
Type
Schools of Medicine
DUNS #
043207562
City
New Haven
State
CT
Country
United States
Zip Code
06520
Lv, Caixia; Stewart, William J; Akanyeti, Otar et al. (2016) Synaptic Ribbons Require Ribeye for Electron Density, Proper Synaptic Localization, and Recruitment of Calcium Channels. Cell Rep 15:2784-95
Arif Pavel, Mahmud; Lv, Caixia; Ng, Courtney et al. (2016) Function and regulation of TRPP2 ion channel revealed by a gain-of-function mutant. Proc Natl Acad Sci U S A 113:E2363-72
Lv, Caixia; Zenisek, David (2014) Big minis from hair cells: mechanism and function. Neuron 83:1229-31
Ricci, Anthony J; Bai, Jun-Ping; Song, Lei et al. (2013) Patch-clamp recordings from lateral line neuromast hair cells of the living zebrafish. J Neurosci 33:3131-4
Lv, Caixia; Gould, Travis J; Bewersdorf, Joerg et al. (2012) High-resolution optical imaging of zebrafish larval ribbon synapse protein RIBEYE, RIM2, and CaV 1.4 by stimulation emission depletion microscopy. Microsc Microanal 18:745-52