Tactile sensation is paramount to how we experience the physical world around us. Species like mice use their facial whiskers to navigate and assess their environment. Although there is a basic understanding of how brainstem trigeminal neurons, the first central relay for whisker-derived signals, respond to passive tactile stimuli, little is known about their activities and functions during active behaviors. Tactile exploration is an active sensing process, which adapts to behavioral purposes, and responses of trigeminal brainstem neurons are likely adjusted accordingly. Furthermore, brainstem projection neurons contribute to two main ascending pathways, lemniscal and paralemniscal, but the functions of these two distinct pathways remain unclear. Our goal for this high-risk exploratory grant application is to develop a chronic in vivo recording preparation, perform recordings from optogenetically identified lemniscal or paralemniscal projection neurons during active behaviors, and use causal manipulations to determine their functions. Recording and manipulating pathway-specific neurons in vivo, and making accurate behavioral measurements in freely moving animals are both challenging. We will use a combination of technological innovations to overcome these challenges. The outcome of this project will establish a platform for future in-depth dissection of how touch sensory information is integrated, transformed and delivered to different processing streams by trigeminal brainstem to generate perception, invoke emotion and/or inform decisions.

Public Health Relevance

How tactile information coming from the face is transformed and delivered to downstream regions by brainstem neurons in behaving animals remains unknown. Using a novel technical approach, we will perform chronic in vivo recording and activity manipulations of identified brainstem projection neurons during active tactile behaviors. This project has the potential to reveal basic neural mechanisms underlying touch sensation and to provide insights on the neural basis of sensory processing deficits observed in various injury and pathological conditions.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Exploratory/Developmental Grants (R21)
Project #
1R21NS101441-01
Application #
9298006
Study Section
Special Emphasis Panel (ZRG1-IFCN-B (03))
Program Officer
Gnadt, James W
Project Start
2017-03-01
Project End
2019-02-28
Budget Start
2017-03-01
Budget End
2018-02-28
Support Year
1
Fiscal Year
2017
Total Cost
$217,504
Indirect Cost
$67,504
Name
Duke University
Department
Neurosciences
Type
Schools of Medicine
DUNS #
044387793
City
Durham
State
NC
Country
United States
Zip Code
27705
McElvain, Lauren E; Friedman, Beth; Karten, Harvey J et al. (2018) Circuits in the rodent brainstem that control whisking in concert with other orofacial motor actions. Neuroscience 368:152-170
Lu, Jinghao; Li, Chunyuan; Singh-Alvarado, Jonnathan et al. (2018) MIN1PIPE: A Miniscope 1-Photon-Based Calcium Imaging Signal Extraction Pipeline. Cell Rep 23:3673-3684
Takatoh, Jun; Prevosto, Vincent; Wang, Fan (2018) Vibrissa sensory neurons: Linking distinct morphology to specific physiology and function. Neuroscience 368:109-114
Bellavance, Marie-Andrée; Takatoh, Jun; Lu, Jinghao et al. (2017) Parallel Inhibitory and Excitatory Trigemino-Facial Feedback Circuitry for Reflexive Vibrissa Movement. Neuron 95:673-682.e4