PUBLICATION

Optical control of zebrafish behavior with halorhodopsin

Authors
Arrenberg, A.B., Del Bene, F., and Baier, H.
ID
ZDB-PUB-091023-22
Date
2009
Source
Proceedings of the National Academy of Sciences of the United States of America   106(42): 17968-17973 (Journal)
Registered Authors
Arrenberg, Aristides, Baier, Herwig, Del Bene, Filippo
Keywords
central pattern generator, channelrhodopsin, Danio rerio, reticulospinal
MeSH Terms
  • Animals
  • Animals, Genetically Modified
  • Bacterial Proteins/genetics
  • Behavior, Animal/physiology*
  • Electrophysiological Phenomena
  • Halorhodopsins/genetics*
  • Halorhodopsins/radiation effects
  • Light
  • Locomotion/physiology
  • Locomotion/radiation effects
  • Luminescent Proteins/genetics
  • Optical Fibers
  • Recombinant Proteins/genetics
  • Recombinant Proteins/radiation effects
  • Rhombencephalon/physiology
  • Rhombencephalon/radiation effects
  • Swimming/physiology
  • Zebrafish/genetics*
  • Zebrafish/physiology*
PubMed
19805086 Full text @ Proc. Natl. Acad. Sci. USA
Abstract
Expression of halorhodopsin (NpHR), a light-driven microbial chloride pump, enables optical control of membrane potential and reversible silencing of targeted neurons. We generated transgenic zebrafish expressing enhanced NpHR under control of the Gal4/UAS system. Electrophysiological recordings showed that eNpHR stimulation effectively suppressed spiking of single neurons in vivo. Applying light through thin optic fibers positioned above the head of a semi-restrained zebrafish larva enabled us to target groups of neurons and to simultaneously test the effect of their silencing on behavior. The photostimulated volume of the zebrafish brain could be marked by subsequent photoconversion of co-expressed Kaede or Dendra. These techniques were used to localize swim command circuitry to a small hindbrain region, just rostral to the commissura infima Halleri. The kinetics of the hindbrain-generated swim command was investigated by combined and separate photo-activation of NpHR and Channelrhodopsin-2 (ChR2), a light-gated cation channel, in the same neurons. Together this "optogenetic toolkit" allows loss-of-function and gain-of-function analyses of neural circuitry at high spatial and temporal resolution in a behaving vertebrate.
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