Conditionally silencing the activity of specific neural ensembles is a powerful approach for mapping the circuits responsible for specific behaviors. While microbial opsin tools currently exist to silence neural activity with light, these tools have significant limitations tha make them unsuitable for applications that require persistent silencing over the course of minutes or hours. Longer term neuronal silencing has been classically achieved by expressing the catalytic light chain of Clostridium neurotoxins, which disrupt neurotransmitter release, however this approach suffers from poor temporal and spatial control. Recent chemogenetic approaches, including designer receptors exclusively activated by designer drugs (DREADDs) have been developed for persistent silencing, but lack the spatiotemporal benefits of optogenetic approaches. Thus, there remains an unmet need for silencing tools that combine the robust and persistent silencing qualities of Clostridium neurotoxin and chemogenetic approaches, with the spatiotemporal control of optogenetics. Here we will develop a completely new toolkit for rapid, extended neural silencing with a single, brief light pulse that can be readiy activated by either single or multiphoton excitation for in vivo systems. Our tools will not only b applicable to neurotransmitter systems, but also to neuromodulatory systems and glial transmission. These powerful tools will complement and extend the existing opto- and chemogenetic silencing toolset by allowing rapid, robust and persistent silencing with a single light pulse. Because our strategy operates on a completely different principle than current tools, it could be multiplexed with existing approaches for complex remote control of circuit activity during behavior.

Public Health Relevance

The goal of this work is to develop new tools to reversibly silence neurons for extended periods of time with spatial and temporal precision. Such tools will complement existing approaches for silencing by enabling precise and extended manipulation of neural circuit activity, allowing researchers to better understand the relevance of specific neural circuits for behavior in normal and disease states.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Exploratory/Developmental Grants (R21)
Project #
1R21EY026363-01
Application #
9055530
Study Section
Special Emphasis Panel (ZEY1)
Program Officer
Wujek, Jerome R
Project Start
2015-09-30
Project End
2017-09-29
Budget Start
2015-09-30
Budget End
2016-09-29
Support Year
1
Fiscal Year
2015
Total Cost
Indirect Cost
Name
University of Colorado Denver
Department
Pharmacology
Type
Schools of Medicine
DUNS #
041096314
City
Aurora
State
CO
Country
United States
Zip Code
80045
Bourke, Ashley M; Bowen, Aaron B; Kennedy, Matthew J (2018) New approaches for solving old problems in neuronal protein trafficking. Mol Cell Neurosci 91:48-66
Liu, Qi; Tucker, Chandra L (2017) Engineering genetically-encoded tools for optogenetic control of protein activity. Curr Opin Chem Biol 40:17-23