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Imaging neural circuit dynamics with a voltage-sensitive fluorescent protein

  • Walther Akemann
  • , Hiroki Mutoh
  • , Amélie Perron
  • , Yun Kyung Park
  • , Yuka Iwamoto
  • , Thomas Knöpfel*
  • *Corresponding author for this work

Research output: Contribution to journalJournal articlepeer-review

210 Citations (Scopus)

Abstract

Population signals from neuronal ensembles in cortex during behavior are commonly measured with EEG, local field potential (LFP), and voltage sensitive dyes. A genetically encoded voltage indicator would be useful for detection of such signals in specific cell types. Here we describe how this goal can be achieved with Butterfly, a voltage sensitive fluorescent protein (VSFP) with a subthreshold detection range and enhancements designed for voltage imaging from single neurons to brain in vivo. VSFP-Butterfly showed reliable membrane targeting, maximum response gain around standard neuronal resting membrane potential, fast kinetics for single-cell synaptic responses, and a high signal-to-noise ratio. Butterfly reports excitatory postsynaptic potentials (EPSPs) in cortical neurons, whisker-evoked responses in barrel cortex, 25-Hz gamma oscillations in hippocampal slices, and 2- to 12-Hz slow waves during brain state modulation in vivo. Our findings demonstrate that cell class-specific voltage imaging is practical with VSFP-Butterfly, and expand the genetic toolbox for the detection of neuronal population dynamics.

Original languageEnglish
Pages (from-to)2323-2337
Number of pages15
JournalJournal of Neurophysiology
Volume108
Issue number8
Early online date18 Jul 2012
DOIs
Publication statusPublished - Oct 2012

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

User-Defined Keywords

  • Cell class specificity
  • EEG
  • Local field potential
  • Optical imaging
  • Voltagesensitive dyes

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