A fundamental goal in the field of neuroscience is to learn how the brain processes sensory information. Understanding how neurons represent sensory stimuli under normal conditions provides the ability to identify compromised components in situations of pathology and develop specific, targeted strategies to treat them. The rodent olfactory system presents many unique advantages to probe sensory coding schemes, including that it is anatomically compact and is fully amenable to all current genetic tools. The field has made great progress since the discovery that families of olfactory receptor genes define many discrete channels of information providing the input to the olfactory bulb through glomeruli1. Still, there is no cohesive theory for how neural codes in the olfactory system build representations of odor features. This proposal approaches the question by proposing a model to link the representations on the input and output levels of the olfactory bulb and testing its predictions experimentally. Specifically, the project seeks to explain the source o the temporal structure observed in responses of the population of mitral and tufted cells (MTCs), each of which receives input from a single glomerulus, and which form the output of the bulb. Our core hypothesis is that the sequence in which an odor activates glomeruli directly influences the sign and timing of responses in the connected MTCs.
Aim 1 tests the basic prediction of the model: that the earlier glomeruli in the spatiotemporal sequence activated by an odor will evoke mainly early, excitatory responses in the connected MTCs, while cells receiving input from later glomeruli will show a heterogeneous set of responses.
Aim 2 will determine if this coding scheme holds over a range of concentrations, as the underlying mechanism in the model predicts.
Aim 3 causally probes whether earlier activation of a glomerulus within the population decreases heterogeneity of responses of its MTCs. The proposed coding scheme has the potential to convey information about the identity of an odor in a way that is tolerant to changes in concentration. These ideas will be tested using recent technological advances in optogenetics and electrophysiology that allow the researchers to target and record odor activity from MTCs that are functionally connected to a specific glomerular channel. The proposed experiments will form the basis of the Primary Investigator's graduate dissertation work and will be carried out over the next 3 years. The Sponsor will provide guidance throughout the process, and particularly with the computational aspects and analyses. The work will be presented at scientific meetings and will be published and made available to the public when completed.

Public Health Relevance

Efficient processing of sensory information is critical for guiding behavior and a rich experience of the environment. A major goal in neuroscience is to understand how the brain represents features of sensory stimuli under normal conditions, which allows us to formulate better strategies to identify and remediate pathology. This proposal aims to unveil fundamental sensory coding schemes of the brain by studying odor representations in the olfactory system.

Agency
National Institute of Health (NIH)
Institute
National Institute on Deafness and Other Communication Disorders (NIDCD)
Type
Predoctoral Individual National Research Service Award (F31)
Project #
5F31DC014903-04
Application #
9331334
Study Section
Special Emphasis Panel (ZDC1)
Program Officer
Rivera-Rentas, Alberto L
Project Start
2015-09-01
Project End
2018-12-31
Budget Start
2017-09-01
Budget End
2018-12-31
Support Year
4
Fiscal Year
2017
Total Cost
Indirect Cost
Name
New York University
Department
Neurosciences
Type
Schools of Arts and Sciences
DUNS #
041968306
City
New York
State
NY
Country
United States
Zip Code
10012
Arneodo, Ezequiel M; Penikis, Kristina B; Rabinowitz, Neil et al. (2018) Stimulus dependent diversity and stereotypy in the output of an olfactory functional unit. Nat Commun 9:1347