Public health relevance: Disruptions in neurodevelopmental events are responsible for a wide range of diseases, including Autism, Fragile X, Lissencephaly, and Kallman's syndrome, that severely affect our society. Before we, as a medical community, can figure out how to treat these devestating disorders, we must first understand on a molecular and cellular level what events have gone wrong developmentally. This study explores the formation of the olfactory pathway as a model system to guide our understanding of critical principles in molecular and cellular development, including axon guidance, cell migration, and cellular differentiation. Only by gaining insight into these fundamental processes will we be able to make progress towards the treatment of neurodevelopmental disorders. Specifically, this proposal focuses on the development of the primary olfactory nerve pathway (ONP), which connects the olfactory sensory neurons (OSNs), which reside in the OE, to the olfactory bulb (OB). The formation of the ONP is comprised of a series of coordinated events that includes the differentiation of cells within the olfactory placode (OP), extension of olfactory sensory neuron (OSN) axons into the mesenchyme, and finally the approach of the axons to the presumptive olfactory bulb (pOB). Our goal is to understand the initial key events central to the proper formation of this pathway and the organization of the axons within the developing olfactory nerve pathway (ONP). Earlier studies noted neuron-like cells within the mesenchyme in close apposition to the OSN axons. Our working hypothesis is that these are OP derived pioneer neurons, which we have termed migrating olfactory placode cells (MOPCs), that contribute to a scaffold or framework utilized by the OSN axons as they establish the initial topography between the OE and OB. Specifically, we hypothesize that MOPCs act as a substrate for the OSN axons during the formation of the ONP and its approach to the pOB. This hypothesis is based on the following: First, throughout the CNS there is evidence for guidepost neurons infiuencing the formation of axon pathways. Second, our preliminary data demonstrate that OSN axons emerge from the OP after the initial transition of MOPCs into the mesenchyme. Third, some MOPCs express odor receptors (ORs) which have been implicated in OSN axon guidance (1). These data suggest that the positioning of the MOPCs is not stochastic but, rather, occurs within a molecularly defined topography that underlies the formation of the olfactory nerve and OSN axon targeting. Our overarching goal is a characterization of the MOPCs and the role(s) they may play in establishing the interface between the olfactory epithelium and pOB.

Agency
National Institute of Health (NIH)
Institute
National Institute on Deafness and Other Communication Disorders (NIDCD)
Type
Individual Predoctoral NRSA for M.D./Ph.D. Fellowships (ADAMHA) (F30)
Project #
1F30DC010324-01
Application #
7751429
Study Section
Communication Disorders Review Committee (CDRC)
Program Officer
Cyr, Janet
Project Start
2009-07-01
Project End
2011-05-31
Budget Start
2009-07-01
Budget End
2010-06-30
Support Year
1
Fiscal Year
2009
Total Cost
$46,176
Indirect Cost
Name
Yale University
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
043207562
City
New Haven
State
CT
Country
United States
Zip Code
06520
Miller, Alexandra M; Maurer, Lydia R; Zou, Dong-Jing et al. (2010) Axon fasciculation in the developing olfactory nerve. Neural Dev 5:20
Mobley, Arie S; Miller, Alexandra M; Araneda, Ricardo C et al. (2010) Hyperpolarization-activated cyclic nucleotide-gated channels in olfactory sensory neurons regulate axon extension and glomerular formation. J Neurosci 30:16498-508
Miller, Alexandra M; Treloar, Helen B; Greer, Charles A (2010) Composition of the migratory mass during development of the olfactory nerve. J Comp Neurol 518:4825-41
Rodriguez-Gil, Diego J; Treloar, Helen B; Zhang, Xiaohong et al. (2010) Chromosomal location-dependent nonstochastic onset of odor receptor expression. J Neurosci 30:10067-75