Rodents use whiskers as their primary tactile sensors. Individual whiskers are innervated by a group of touch sensory neurons located in the trigeminal ganglion, and are mapped onto the brain by the central axons from the same set of trigeminal neurons. The discovery of the whisker- related large modular structures (barrelettes in the hindbrain, barreloids in the thalamus and barrels in the cortex) in 1970s made the trigeminal-whisker system a popular prototypic model for studying somatosensory maps and touch sensory circuits. Yet to date, we still have limited knowledge of the precise neural circuits assembled inside each whisker-representing unit. The objective of this proposal is to dissect the micro-circuits formed by different classes of touch sensory neurons within individual barrelettes, and to begin to identify the molecular mechanisms controlling the precise assembly of these barrelette circuits. These studies will provide the much- needed knowledge for future understanding of somatosensory information coding and processing and ultimately sensory perception. The mechanisms uncovered in this study will also have broad implications for understanding neuropathological diseases associated with abnormal wiring in the somatosensory system such as Autism and neuropathic orofacial pain.

Public Health Relevance

Compared with advance in the visual and olfactory sensory system, we know relatively little about the precise synaptic connections made by diverse somatosensory neurons and the mechanisms controlling the assembly of somatosensory circuits. In this grant proposal, we will use the mouse trigeminal system as a model to dissect the detailed neural circuits representing the tactile organs - the whiskers, and to begin to identify the molecular mechanisms controlling the formation of touch sensory circuits inside the mouse brain. The circuits and mechanisms uncovered in this study will not only reveal general principles underlying the organization and the development of the somatosensory system, but also will have broad implications for understanding neuropathological diseases associated with abnormal wiring in the somatosensory system such as Autism diseases and the neuropathic orofacial pain.

Agency
National Institute of Health (NIH)
Institute
National Institute of Dental & Craniofacial Research (NIDCR)
Type
Research Project (R01)
Project #
5R01DE019440-04
Application #
8291138
Study Section
Sensorimotor Integration Study Section (SMI)
Program Officer
Kusiak, John W
Project Start
2009-07-01
Project End
2014-06-30
Budget Start
2012-07-01
Budget End
2013-06-30
Support Year
4
Fiscal Year
2012
Total Cost
$370,771
Indirect Cost
$133,097
Name
Duke University
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
044387793
City
Durham
State
NC
Country
United States
Zip Code
27705
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da Silva, Susana; Wang, Fan (2011) Retrograde neural circuit specification by target-derived neurotrophins and growth factors. Curr Opin Neurobiol 21:61-7
da Silva, Susana; Hasegawa, Hiroshi; Scott, Alexandra et al. (2011) Proper formation of whisker barrelettes requires periphery-derived Smad4-dependent TGF-beta signaling. Proc Natl Acad Sci U S A 108:3395-400

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