Regulation of axonal and synaptic signaling in interneurons

NIH RePORTER · NIH · R35 · $523,835 · view on reporter.nih.gov ↗

Abstract

Summary Neurons encode a wide variety of signals, each with specific relevance for translating a sensory response or memory into behavior. How are cells and synapses optimized to meet these needs? Our work has used in vitro model systems to understand such specializations of function at the level of the dendrite, the axon initial segment and the nerve terminal. The lab's studies have stretched the classical views of neuronal function, for example by showing how neurotransmitter receptors in the axon initial segment and in the nerve terminal have unique roles for modifying axon and synaptic communication. In this proposal, we will turn to a new view of the role of the axon. Beyond its function in the one-way transmission of spikes, we will examine how subthreshold signals generated in the soma, the axon or the terminal spread along the axon in the forward and reverse directions to modify the spike and its propagation. Additionally, we will examine how calcium release mechanism modulate excitation in neonatal brain. Key to these aims will be the use of carefully selected mouse lines that feature sparse fluorescent labeling of neurons with fluorophores that clearly reveal each compartment of the neuron in living brain slices, from dendrite to nerve terminal. The research should reveal new dimensions of signaling that operate in parallel with the action potential, particularly in interneurons in neural microcircuits

Key facts

NIH application ID
10150116
Project number
5R35NS116798-02
Recipient
OREGON HEALTH & SCIENCE UNIVERSITY
Principal Investigator
LAURENCE O TRUSSELL
Activity code
R35
Funding institute
NIH
Fiscal year
2021
Award amount
$523,835
Award type
5
Project period
2020-05-01 → 2028-04-30