The goal of this project is to understand how neural signals are transmitted in the retina, from photoreceptors through bipolar neurons to the ganglion cells. Because of the central position of bipolar neurons in this signal path, the synaptic contacts made by bipolar neurons are a vital link in the transmission and processing of visual information. Therefore, one major focus of this project is the mechanism of neurotransmitter release from synaptic terminals of retinal bipolar neurons. Chemical neurotransmitter is released from synaptic terminals via exocytosis of synaptic vesicles, and the membrane of fused vesicles is then retrieved by endocytosis. These fundamental processes of synaptic exocytosis and endocytosis will be examined in multidisciplinary experiments combining optical, electrophysiological, molecular, and anatomical approaches. Because neurotransmitter release is controlled by presynaptic calcium influx, experiments will also be conducted to determine the mechanisms controlling internal calcium in synaptic terminals, including the calcium channels that support calcium entry and the extrusion and buffering mechanisms that regulate intracellular calcium concentration. ? ? Ultimately, the visual signal leaving the retina is encoded in action potentials in the ganglion cell axons of the optic nerve. The second major focus of the project is the channels that generate action potentials, voltage-dependent sodium channels. Knowledge of the physiological and molecular properties of these channels is required to understand the encoding and transmission of visual information. Multiple sodium-channel genes are expressed in the retina, and experiments will be conducted to examine the differential targeting of sodium channel isoforms in retinal neurons. The functional implications of the localization of particular sodium channel isoforms to specific regions of ganglion cell axons will also be investigated. The roles of voltage-gated sodium channels in the dendritic propagation of synaptic signals will also be studied in cells that do not produce action potentials, such as retinal bipolar neurons. These two lines of research will provide information about basic aspects of retinal signal processing. The results will also be of general significance for neuronal function in other parts of the nervous system outside the retina.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
5R01EY003821-26
Application #
7110941
Study Section
Special Emphasis Panel (ZRG1-VISC (01))
Program Officer
Hunter, Chyren
Project Start
1981-08-01
Project End
2007-11-30
Budget Start
2006-09-20
Budget End
2007-11-30
Support Year
26
Fiscal Year
2006
Total Cost
$367,408
Indirect Cost
Name
State University New York Stony Brook
Department
Neurosciences
Type
Schools of Medicine
DUNS #
804878247
City
Stony Brook
State
NY
Country
United States
Zip Code
11794
Vaithianathan, Thirumalini; Henry, Diane; Akmentin, Wendy et al. (2016) Nanoscale dynamics of synaptic vesicle trafficking and fusion at the presynaptic active zone. Elife 5:
Vaithianathan, Thirumalini; Henry, Diane; Akmentin, Wendy et al. (2015) Functional roles of complexin in neurotransmitter release at ribbon synapses of mouse retinal bipolar neurons. J Neurosci 35:4065-70
Vaithianathan, Thirumalini; Matthews, Gary (2014) Visualizing synaptic vesicle turnover and pool refilling driven by calcium nanodomains at presynaptic active zones of ribbon synapses. Proc Natl Acad Sci U S A 111:8655-60
Vaithianathan, Thirumalini; Akmentin, Wendy; Henry, Diane et al. (2013) The ribbon-associated protein C-terminal-binding protein 1 is not essential for the structure and function of retinal ribbon synapses. Mol Vis 19:917-26
Vaithianathan, Thirumalini; Zanazzi, George; Henry, Diane et al. (2013) Stabilization of spontaneous neurotransmitter release at ribbon synapses by ribbon-specific subtypes of complexin. J Neurosci 33:8216-26
Vega, Ana V; Avila, Guillermo; Matthews, Gary (2013) Interaction between the transcriptional corepressor Sin3B and voltage-gated sodium channels modulates functional channel expression. Sci Rep 3:2809
Snellman, Josefin; Mehta, Bhupesh; Babai, Norbert et al. (2011) Acute destruction of the synaptic ribbon reveals a role for the ribbon in vesicle priming. Nat Neurosci 14:1135-41
Hunanyan, Arsen S; Alessi, Valentina; Patel, Samik et al. (2011) Alterations of action potentials and the localization of Nav1.6 sodium channels in spared axons after hemisection injury of the spinal cord in adult rats. J Neurophysiol 105:1033-44
Zanazzi, George; Matthews, Gary (2010) Enrichment and differential targeting of complexins 3 and 4 in ribbon-containing sensory neurons during zebrafish development. Neural Dev 5:24
Matthews, Gary; Fuchs, Paul (2010) The diverse roles of ribbon synapses in sensory neurotransmission. Nat Rev Neurosci 11:812-22

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