The perception of odors begins in the olfactory epithelium when odorant ligands bind to molecular receptors expressed on the cilia of the olfactory sensory neurons, each of which expresses only 1 of ~1200 candidate receptors. As the sensory neuron axons exit the epithelium they progress over the surface of the olfactory bulb and all of the axons coming from neurons expressing the same odorant receptor converge into only 2/3 glomeruli/olfactory bulb. However, the convergence primary afferent axons within the glomerulus and the discrete local circuitry modulating afferent input remains uncertain Despite a long history of interest, we remain woefully ignorant of the most fundamental features of cellular and synaptic organization within glomeruli: What is the distribution of the dendritic processes of projection neurons versus interneurons within the glomerulus? What is the 3-dimensional topography of synapses along dendrites and in the core versus the periphery of the glomerulus? What is the nature and composition of non-synaptic interactions among dendrites? With the recent development of Serial Block-Face Scanning Electron Microscopy (sbSEM) the ability to serially reconstruct glomeruli at the ultrastructural level, to establish the glomerular connectome, these and other questions are within our grasp. To begin addressing the utility of sbSEM in understanding olfactory bulb circuitry we begin with with the following: 1) The hypothesis that the dendrodendritic synapses between glomerular interneurons and projection neurons are reciprocal. The dendritic Gray Type I and II synapses in glomeruli appear unipolar and isolated. They are presumed to be reciprocal based on physiology, but if there is reciprocity, it is not known if the ratio is 1:1 or unequal. Moreover, it is not clear if they mediate self- or lateral inhibition. 2) The hypothesis that axodendritic (excitatory) and dendrodendritic (inhibitory) synapses differentially localize to the distal versus the proximal dendritic segments of projection neurons. Gate-keeping inhibitory synapses are often found at dendritic branch points, but whether that holds true in glomeruli must be empirically determined using comprehensive 3D dendritic reconstructions. 3) The hypothesis that single OSN axon establish divergent synaptic connections with dendrites from different neurons. Does a single axon repeatedly contact the same dendrite, or is it divergent? While the question seems simple, the answer will provide new insight into the roles of feed- forward and feed-back processing. 4) The location(s) of presynaptic inhibition on OSN axons. Electrophysiological analyses support presynaptic inhibition by showing, for example, that GABAB agonists decrease Ca++ influx into the axon terminals. However, the site of synaptic apposition is not known. Using sbSEM to address these questions will resolve fundamental controversies regarding processing of odors within the glomerulus and provide the foundation for further studies of development and plasticity.

Public Health Relevance

This proposal will pursue a comprehensive understanding of the structural organization of the olfactory bulb glomerulus. The glomeruli are the first site of odor processing in the olfactory system and receive the converged input from olfactory sensory neurons expressing the same odor receptor. Therefore, each of the 3,700 glomeruli in the olfactory bulb has a unique molecular signature. Prior work characterized the fundamental synaptic targets of the sensory neuron axons, but an integrated blueprint of the organization of the glomerulus has been elusive. Now, with the introduction of Serial Block-Face Scanning Electron Microscopy (sbSEM) the glomerular connectome is within our grasp. This proposal seeks to establish the utility of sbSEM to full reconstruct the 3-dimensional organization of processes within the glomeruli and the topographical distribution of both the primary afferent and local circuit synapses. These data will provide new insight into the circuitry underlying odor processing and are likely lead to improvements in strategies for treating traumatic and genetic perturbations of neuronal circuits.

Agency
National Institute of Health (NIH)
Institute
National Institute on Deafness and Other Communication Disorders (NIDCD)
Type
Exploratory/Developmental Grants (R21)
Project #
1R21DC015438-01
Application #
9151518
Study Section
Somatosensory and Chemosensory Systems Study Section (SCS)
Program Officer
Sullivan, Susan L
Project Start
2016-06-01
Project End
2018-05-31
Budget Start
2016-06-01
Budget End
2017-05-31
Support Year
1
Fiscal Year
2016
Total Cost
$251,126
Indirect Cost
$101,126
Name
Yale University
Department
Neurosurgery
Type
Schools of Medicine
DUNS #
043207562
City
New Haven
State
CT
Country
United States
Zip Code
06520
Martin-Lopez, Eduardo; Meller, Sarah J; Greer, Charles A (2018) Development of piriform cortex interhemispheric connections via the anterior commissure: progressive and regressive strategies. Brain Struct Funct 223:4067-4085
Finger, Thomas E; Bartel, Dianna L; Shultz, Nicole et al. (2017) 5HTR3A-driven GFP labels immature olfactory sensory neurons. J Comp Neurol 525:1743-1755