The main objective of this project is to elucidate the mechanisms underlying axon guidance in the olfactory system, using rodent models. Most mammalian species, including humans, have the ability to distinguish thousands of different odors. This ability is encoded in the organized connections made between olfactory sensory neurons in the nasal cavity and CNS neurons in the olfactory bulb. Axons from sensory neurons distributed widely in the nasal cavity converge onto a small number of targets called glomeruli that have fixed positions in the olfactory bulb. Conversely, axons from neighboring sensory neurons diverge to broadly defined zones in the olfactory bulb. This proposal focuses on the cells and extracellular matrix proteins that occupy axon pathways and the olfactory nerve layer that surrounds the olfactory bulb. The main cell type present in these regions is a special type of glial cell (ensheathing cell) that is unique to the olfactory system. It is hypothesized that ensheathing cells are molecularly heterogeneous and therefore present a differential environment to olfactory axons as they extend into the nerve layer of the olfactory bulb. Specific subpopulations of ensheathing cells have been shown to simultaneously present a permissive and non-permissive environment to unique subsets of olfactory axons. We propose to construct a map of the permissive and non-permissive regions of the nerve layer, defining the expression of guidance cues and the axons that they regulate. We will perturb interactions between axons and guidance cues in the nerve layer in vivo and in slice cultures of embryonic olfactory tissue in order to demonstrate functional activity in an intact system. We will also analyze development of ensheathing cells, in particular, the regulation of migration of precursor cells from the olfactory epithelium to the nerve layer of the olfactory bulb. These studies are intended to broaden our knowledge of mechanisms used to organize connections in the mammalian nervous system.

Agency
National Institute of Health (NIH)
Institute
National Institute on Deafness and Other Communication Disorders (NIDCD)
Type
Research Project (R01)
Project #
3R01DC000953-11S1
Application #
6787467
Study Section
Integrative, Functional and Cognitive Neuroscience 8 (IFCN)
Program Officer
Davis, Barry
Project Start
1992-04-01
Project End
2006-03-31
Budget Start
2003-08-15
Budget End
2004-03-31
Support Year
11
Fiscal Year
2003
Total Cost
$46,590
Indirect Cost
Name
University of Massachusetts Medical School Worcester
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
603847393
City
Worcester
State
MA
Country
United States
Zip Code
01655
Henion, Timothy R; Schwarting, Gerald A (2014) N-linked polylactosamine glycan synthesis is regulated by co-expression of ?3GnT2 and GCNT2. J Cell Physiol 229:471-8
Henion, Timothy R; Madany, Pasil A; Faden, Ashley A et al. (2013) ?3GnT2 null mice exhibit defective accessory olfactory bulb innervation. Mol Cell Neurosci 52:73-86
Knott, Thomas K; Madany, Pasil A; Faden, Ashley A et al. (2012) Olfactory discrimination largely persists in mice with defects in odorant receptor expression and axon guidance. Neural Dev 7:17
Schwarting, Gerald A; Henion, Timothy R (2011) Regulation and function of axon guidance and adhesion molecules during olfactory map formation. J Cell Biochem 112:2663-71
Henion, Timothy R; Faden, Ashley A; Knott, Thomas K et al. (2011) ?3GnT2 maintains adenylyl cyclase-3 signaling and axon guidance molecule expression in the olfactory epithelium. J Neurosci 31:6576-86
Schwarting, Gerald A; Henion, Timothy R (2008) Olfactory axon guidance: the modified rules. J Neurosci Res 86:11-7
Schwarting, Gerald A; Gridley, Thomas; Henion, Timothy R (2007) Notch1 expression and ligand interactions in progenitor cells of the mouse olfactory epithelium. J Mol Histol 38:543-53
Henion, Timothy R; Schwarting, Gerald A (2007) Patterning the developing and regenerating olfactory system. J Cell Physiol 210:290-7
Schwarting, Gerald A; Henion, Timothy R; Nugent, J David et al. (2006) Stromal cell-derived factor-1 (chemokine C-X-C motif ligand 12) and chemokine C-X-C motif receptor 4 are required for migration of gonadotropin-releasing hormone neurons to the forebrain. J Neurosci 26:6834-40
Henion, Timothy R; Raitcheva, Denitza; Grosholz, Robert et al. (2005) Beta1,3-N-acetylglucosaminyltransferase 1 glycosylation is required for axon pathfinding by olfactory sensory neurons. J Neurosci 25:1894-903

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