The mammalian olfactory epithelium does two remarkable things with its olfactory sensory neurons. These neurons detect odorants, translating the structure of volatile chemicals into a neural information code, and the epithelium can replace these neurons even if they are completely eliminated. These properties are of significant interest for both basic and applied neuroscience research. The goal of this project is to generate a finely detailed description of the phenotypes of the mature olfactory sensory neurons and their immediate progenitor cells, then use this description to predict critical steps in the molecular mechanisms that lead to the genesis of these neurons, their ability to detect certain odors, and their ability to survive in their exposed position.
The first aim of this project combines a system-wide view of gene expression with our ability to purify certain cell types so that we can assign gene expression patterns and the biological processes they represent to their correct homes in the cells of the epithelium.
The second aim takes advantage of predictions about genes whose products regulate the activity of other genes made by our preliminary data. We will test whether targeted knockout of six of these regulator genes, all expressed by immature olfactory sensory neurons, causes deficits in either the production of mature neurons or in critical functions of these neurons.
The third aim i s based on our belief that within the expression patterns we observe in olfactory sensory neurons are sets of genes responsible for survival of the neurons. We will use odor stimulation, which is known to enhance survival, to increase the activity of pro-survival genes (or suppress anti-survival genes) so that they can be detected. This project is an integrated approach to understanding the genes whose activity is important for generating the phenotype of mature olfactory sensory neurons and then maintaining these cells in the face of significant challenges.

Agency
National Institute of Health (NIH)
Institute
National Institute on Deafness and Other Communication Disorders (NIDCD)
Type
Research Project (R01)
Project #
3R01DC002736-12S1
Application #
7852762
Study Section
Special Emphasis Panel (ZRG1-IFCN-K (03))
Program Officer
Davis, Barry
Project Start
2009-07-17
Project End
2011-06-30
Budget Start
2009-07-17
Budget End
2011-06-30
Support Year
12
Fiscal Year
2009
Total Cost
$153,308
Indirect Cost
Name
University of Kentucky
Department
Physiology
Type
Schools of Medicine
DUNS #
939017877
City
Lexington
State
KY
Country
United States
Zip Code
40506
Zhang, Guangfan; Titlow, William B; Biecker, Stephanie M et al. (2016) Lhx2 Determines Odorant Receptor Expression Frequency in Mature Olfactory Sensory Neurons. eNeuro 3:
McClintock, Timothy S (2015) Odorant Receptor Gene Choice. ChemoSense 16:3-13
McClintock, Timothy S; Adipietro, Kaylin; Titlow, William B et al. (2014) In vivo identification of eugenol-responsive and muscone-responsive mouse odorant receptors. J Neurosci 34:15669-78
Fischl, Adrian M; Heron, Paula M; Stromberg, Arnold J et al. (2014) Activity-dependent genes in mouse olfactory sensory neurons. Chem Senses 39:439-49
Nickell, Melissa D; Breheny, Patrick; Stromberg, Arnold J et al. (2012) Genomics of mature and immature olfactory sensory neurons. J Comp Neurol 520:2608-29
Sammeta, Neeraja; Hardin, Debra L; McClintock, Timothy S (2010) Uncx regulates proliferation of neural progenitor cells and neuronal survival in the olfactory epithelium. Mol Cell Neurosci 45:398-407
McClintock, Timothy S (2010) Achieving singularity in mammalian odorant receptor gene choice. Chem Senses 35:447-57
McIntyre, Jeremy C; Titlow, William B; McClintock, Timothy S (2010) Axon growth and guidance genes identify nascent, immature, and mature olfactory sensory neurons. J Neurosci Res 88:3243-56
Sammeta, Neeraja; McClintock, Timothy S (2010) Chemical stress induces the unfolded protein response in olfactory sensory neurons. J Comp Neurol 518:1825-36
McIntyre, Jeremy C; Bose, Soma C; Stromberg, Arnold J et al. (2008) Emx2 stimulates odorant receptor gene expression. Chem Senses 33:825-37

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