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Capturing and Manipulating Activated Neuronal Ensembles with CANE Delineates a Hypothalamic Social-Fear Circuit
Abstract
© 2016 Elsevier Inc.We developed a technology (capturing activated neuronal ensembles
[CANE]) to label, manipulate, and transsynaptically trace neural circuits that are
transiently activated in behavioral contexts with high efficiency and temporal precision.
CANE consists of a knockin mouse and engineered viruses designed to specifically infect
activated neurons. Using CANE, we selectively labeled neurons that were activated
by either fearful or aggressive social encounters in a hypothalamic subnucleus previously
known as a locus for aggression, and discovered that social-fear and aggression neurons
are intermixed but largely distinct. Optogenetic stimulation of CANE-captured social-fear
neurons (SFNs) is sufficient to evoke fear-like behaviors in normal social contexts,
whereas silencing SFNs resulted in reduced social avoidance. CANE-based mapping of
axonal projections and presynaptic inputs to SFNs further revealed a highly distributed
and recurrent neural network. CANE is a broadly applicable technology for dissecting
causality and connectivity of spatially intermingled but functionally distinct ensembles.
Type
Journal articlePermalink
https://hdl.handle.net/10161/13276Published Version (Please cite this version)
10.1016/j.neuron.2016.10.015Publication Info
Sakurai, Katsuyasu; Zhao, Shengli; Takatoh, Jun; Rodriguez, Erica; Lu, Jinghao; Leavitt,
Andrew D; ... Wang, Fan (2016). Capturing and Manipulating Activated Neuronal Ensembles with CANE Delineates a Hypothalamic
Social-Fear Circuit. Neuron, 92(4). pp. 739-753. 10.1016/j.neuron.2016.10.015. Retrieved from https://hdl.handle.net/10161/13276.This is constructed from limited available data and may be imprecise. To cite this
article, please review & use the official citation provided by the journal.
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Show full item recordScholars@Duke
Fan Wang
Adjunct Professor in the Department of Neurobiology
My lab studies neural circuit basis of sensory perception. Specifically we are interested
in determining neural circuits underlying (1) active touch sensation including tactile
processing stream and motor control of touch sensors on the face; (2) pain sensation
including both sensory-discriminative and affective aspects of pain; and (3) general
anesthesia including the active pain-suppression process. We use a combination of
genetic, viral, electrophysiology, and in vivo imaging (in f

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