TY - JOUR
T1 - Sonogenetics is a non-invasive approach to activating neurons in Caenorhabditis elegans
AU - Ibsen, Stuart
AU - Tong, Ada
AU - Schutt, Carolyn
AU - Esener, Sadik
AU - Chalasani, Sreekanth H.
N1 - Funding Information:
We thank S. Xu for providing the trp-4 cDNA, C. Bargmann, S. Xu and the CGC for strains, and N. Chronis and the Chronis lab for insightful discussions. We also thank L. Hale, S. Leinwand and C. Profaci, and members of the Chalasani and Esener labs, for helpful comments and suggestions on the manuscript. A Salk Institute Pioneer Fund Postdoctoral Fellowship (S.I.) and a Salk Institute Innovation Grant, The Rita Allen Foundation, The W.M. Keck Foundation and NIH R01MH096881-03 to S.H.C. supported this work.
Publisher Copyright:
© 2015 Macmillan Publishers Limited. All rights reserved.
PY - 2015/9/15
Y1 - 2015/9/15
N2 - A major challenge in neuroscience is to reliably activate individual neurons, particularly those in deeper brain regions. Current optogenetic approaches require invasive surgical procedures to deliver light of specific wavelengths to target cells to activate or silence them. Here, we demonstrate the use of low-pressure ultrasound as a non-invasive trigger to activate specific ultrasonically sensitized neurons in the nematode, Caenorhabditis elegans. We first show that wild-type animals are insensitive to low-pressure ultrasound and require gas-filled microbubbles to transduce the ultrasound wave. We find that neuron-specific misexpression of TRP-4, the pore-forming subunit of a mechanotransduction channel, sensitizes neurons to ultrasound stimulus, resulting in behavioural outputs. Furthermore, we use this approach to manipulate the function of sensory neurons and interneurons and identify a role for PVD sensory neurons in modifying locomotory behaviours. We suggest that this method can be broadly applied to manipulate cellular functions in vivo.
AB - A major challenge in neuroscience is to reliably activate individual neurons, particularly those in deeper brain regions. Current optogenetic approaches require invasive surgical procedures to deliver light of specific wavelengths to target cells to activate or silence them. Here, we demonstrate the use of low-pressure ultrasound as a non-invasive trigger to activate specific ultrasonically sensitized neurons in the nematode, Caenorhabditis elegans. We first show that wild-type animals are insensitive to low-pressure ultrasound and require gas-filled microbubbles to transduce the ultrasound wave. We find that neuron-specific misexpression of TRP-4, the pore-forming subunit of a mechanotransduction channel, sensitizes neurons to ultrasound stimulus, resulting in behavioural outputs. Furthermore, we use this approach to manipulate the function of sensory neurons and interneurons and identify a role for PVD sensory neurons in modifying locomotory behaviours. We suggest that this method can be broadly applied to manipulate cellular functions in vivo.
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U2 - 10.1038/ncomms9264
DO - 10.1038/ncomms9264
M3 - Article
C2 - 26372413
AN - SCOPUS:84941769671
SN - 2041-1723
VL - 6
JO - Nature communications
JF - Nature communications
M1 - 8264
ER -