The olfactory system of mammals is thought to be capable of distinguishing among thousands of odors. Subtle differences in the molecular structure of some odors can lead to a dramatic change in odor perception. It is now known that the first step in olfactory discrimination involves the interaction of odors with odorant receptors on sensory neurons in the nasal cavity. How the brain determines which receptors have been activated remains a mystery. However, as in most sensory systems, the olfactory system probably uses defined spatial patterns of receptor activation to make connections in the brain. The overall objectives of this proposal are to determine the identity, structure and function of molecules that participate in the spatial organization of connections between the olfactory sensory neurons in the nasal cavity and their axon termination sites in the olfactory bulb. The investigators have proposed three different mechanisms that may be important in the formation of specific olfactory connections, and during the continual neural renewal that occurs in the olfactory system. 1) A coarse topographic map divides the main olfactory system into at least four compartments and the accessory olfactory system into two compartments. They will analyze the determinants of compartmentalization by isolating and characterizing the molecules that restrict the termination sites of axon subsets. The ability of these molecules to influence axon trajectories will be tested on primary cell cultures of olfactory neurons. The structural determinants of compartmentalization will be investigated using light and electron microscopy in conjunction with immunocytochemical studies of intact olfactory bulbs. 2) There is a spatial and temporal pattern of expression of axonal and extracellular matrix adhesion molecules that provides a basis for subsets of axons to grow along designated pathways. One of these adhesion mechanisms in the olfactory system utilizes an endogenous carbohydrate binding protein, L-14, that is capable of inducing axon-axon and axon-matrix interactions. The investigators will analyze the role of this adhesion mechanism during development of olfactory connections, using mutant mice deficient in the extracellular matrix glycoprotein merosin, a key component of this adhesion mechanism. 3) Neuronal activity plays a role in stabilizing specific connections, leading to refinement of a coarse olfactory map. They will analyze the effects of changing neuronal activity through sensory deprivation on the precision of connections made by a small group of chemically defined neurons. The developmental relationship of the olfactory system and the forebrain is clinically significant. X-linked Kallmann syndrome is caused by a defect in the development of the olfactory system. These studies will provide insight into the molecular and cellular basis of olfactory structure and function and will illuminate specific mechanisms of axonal growth in normal and abnormal nervous systems.

Agency
National Institute of Health (NIH)
Institute
National Institute on Deafness and Other Communication Disorders (NIDCD)
Type
Research Project (R01)
Project #
5R01DC000953-08
Application #
2900033
Study Section
Neurology C Study Section (NEUC)
Project Start
1992-04-01
Project End
2000-06-30
Budget Start
1999-04-01
Budget End
2000-06-30
Support Year
8
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Eunice Kennedy Shriver Center Mtl Retardatn
Department
Type
DUNS #
City
Waltham
State
MA
Country
United States
Zip Code
02254
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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