Grants and Contracts Details
Description
This postdoctoral F32 Kirschstein NRSA proposes a comprehensive research and
training plan in the study of neurogenesis and axon guidance in the olfactory system with
relevance to neural regeneration therapies. Failure of the damaged nervous system to
repair itself has debilitating consequences for millions of people worldwide.
Regeneration therapies are focused on restoring damaged circuitry by regrowth and
guidance of the axons of spared neurons or replacement of dead neurons. The olfactory
system provides a useful model to study cell replacement and axon targeting in a mature
nervous system. Although the mechanisms by which olfactory sensory neuron (OSN)
axons are targeted to the olfactory bulb remain largely unknown, the anterior-posterior
patterning of glomerular convergence in the bulb correlates with neuronal levels of cAMP
and altered expression of activity-dependent guidance cues. However, direct evidence of
the involvement of cAMP in axon targeting and the genetic mechanisms involved are
lacking. The specific aims of this proposal will test the hypothesis that cAMP plays a
definitive role in glomerular convergence ofaxons in the bulb. If this idea is correct, then
transgenic mice exhibiting sustained increases in cAMP in immature OSNs should show
altered glomerular convergence and position. Aim 1 will use transgenic mice that
express a constitutively active G-protein-coupled receptor, GPR12, in immature OSNs.
GPR12 couples to Gas, adenylyl cyclase and cAMP production. To follow specific
populations of OSN axons, GPR12 transgenic mice will be crossed with OR-tauLacZ
mice, such as the M71-tauLacZ strain. This will allow visualization of the coalescence of
OSN axons. Aim 2 will investigate changes in cAMP-mediated downstream signaling
events that lead to alterations in gene expression. Identification of cAMP driven signal
transduction in immature OSNs will help to elucidate mechanisms that control the
position of OSN axon convergence in the olfactory bulb. Aim 3 will test whether cAMP
overexpression will rescue the lack of target innervation in mice lacking the emx2 gene.
The results from these studies will provide novel insight into the role of cAMP signaling
in OSN axon growth and convergence in the olfactory bulb.
Status | Finished |
---|---|
Effective start/end date | 9/1/10 → 8/31/13 |
Funding
- National Institute on Deafness & Other Communications: $55,670.00
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