Evidence map›Paper›PMID 26468193›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2015

All-Optical Interrogation of Neural Circuits.

Valentina Emiliani, Adam E Cohen, Karl Deisseroth, Michael Häusser

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 195 papers.

0numbers the graph read from it
0cells of the map it votes in
195citing papers in PubMed
17.3field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

195 citing papers in PubMed, 381 citations in OpenAlex.

  1. Article
  2. Review
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  4. Article
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  6. Article
  7. Editorial: The diversity of the plasticitome.Frontiers in synaptic neuroscience · 2026
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  11. Review
  12. Miniaturized widefield microscope for high speed in vivo voltage imaging.bioRxiv : the preprint server for biology · 2025
    Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. A large field of view 2- and 3-photon microscope.Light, science & applications · 2025
    Article
  20. Luminos: open-source software for bidirectional microscopy.bioRxiv : the preprint server for biology · 2025
    Article

135 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 4 institutions in 4 countries.

Valentina EmilianiNeurophotonics Laboratory, CNRS UMR 8250, Paris Descartes University, 75270 Paris Cedex 06, France, valentina.emiliani@parisdescartes.fr cohen@chemistry.harvard.edu deissero@stanford.edu m.hausser@ucl.ac.uk.
Adam E CohenDepartments of Chemistry and Chemical Biology and Physics, Howard Hughes Medical Institute and Harvard University, Cambridge, Massachusetts 02138, valentina.emiliani@parisdescartes.fr cohen@chemistry.harvard.edu deissero@stanford.edu m.hausser@ucl.ac.uk.
Karl DeisserothDepartment of Bioengineering and Howard Hughes Medical Institute, Stanford University, Stanford, California 94305, and valentina.emiliani@parisdescartes.fr cohen@chemistry.harvard.edu deissero@stanford.edu m.hausser@ucl.ac.uk.
Michael HäusserWolfson Institute for Biomedical Research and Department of Neuroscience, Physiology and Pharmacology, University College London, London WC1E 6BT, United Kingdom valentina.emiliani@parisdescartes.fr cohen@chemistry.harvard.edu deissero@stanford.edu m.hausser@ucl.ac.uk.
Bioengineering Center · RUDélégation Paris 5 · FRHoward Hughes Medical Institute · USUniversity College London · GB

Funding

Structural and molecular identification of circuitry underlying joint processing of motivation and aversionR37DA035377 · NIDA · STANFORD UNIVERSITY · PI DEISSEROTH, KARL A. · 2013 to 2022
$6.2M
Optical sensing of voltage, pH, and small molecules using microbial rhodopsinsDP2OD007428 · OD · HARVARD UNIVERSITY · PI COHEN, ADAM EZRA · 2010 to 2010
$2.5M
Engineering Microbial Rhodopsins as Optical Voltage SensorsR01EB012498 · NIBIB · HARVARD UNIVERSITY · PI COHEN, ADAM EZRA · 2011 to 2014
$1.5M
Three Dimensional Holography for Parallel Multi-target Optogenetic Circuit ManipulationU01NS090501 · NINDS · PIERRE AND MARIE CURIE UNIVERSITY · PI EMILIANI, VALENTINA, MARRE, OLIVIER · 2014 to 2016
$941k
Howard Hughes Medical InstituteNIBIB NIH HHS R01 EB012498NIBIB NIH HHS R01EB012498-02NIDA NIH HHS R37 DA035377NIH HHS DP2 OD007428NIH HHS DP2OD007428NINDS NIH HHS 1-U01-NS090501-01NINDS NIH HHS U01 NS090501Wellcome Trust 094077
6 · The paper itself

Abstract

There have been two recent revolutionary advances in neuroscience: First, genetically encoded activity sensors have brought the goal of optical detection of single action potentials in vivo within reach. Second, optogenetic actuators now allow the activity of neurons to be controlled with millisecond precision. These revolutions have now been combined, together with advanced microscopies, to allow "all-optical" readout and manipulation of activity in neural circuits with single-spike and single-neuron precision. This is a transformational advance that will open new frontiers in neuroscience research. Harnessing the power of light in the all-optical approach requires coexpression of genetically encoded activity sensors and optogenetic probes in the same neurons, as well as the ability to simultaneously target and record the light from the selected neurons. It has recently become possible to combine sensors and optical strategies that are sufficiently sensitive and cross talk free to enable single-action-potential sensitivity and precision for both readout and manipulation in the intact brain. The combination of simultaneous readout and manipulation from the same genetically defined cells will enable a wide range of new experiments as well as inspire new technologies for interacting with the brain. The advances described in this review herald a future where the traditional tools used for generations by physiologists to study and interact with the brain-stimulation and recording electrodes-can largely be replaced by light. We outline potential future developments in this field and discuss how the all-optical strategy can be applied to solve fundamental problems in neuroscience. SIGNIFICANCE STATEMENT: This review describes the nexus of dramatic recent developments in optogenetic probes, genetically encoded activity sensors, and novel microscopies, which together allow the activity of neural circuits to be recorded and manipulated entirely using light. The optical and protein engineering strategies that form the basis of this "all-optical" approach are now sufficiently advanced to enable single-neuron and single-action potential precision for simultaneous readout and manipulation from the same functionally defined neurons in the intact brain. These advances promise to illuminate many fundamental challenges in neuroscience, including transforming our search for the neural code and the links between neural circuit activity and behavior.

Indexed as

OptogeneticsAnimalsBrainHumansNerve NetNeuronscalcium imaginggenetically encoded calcium sensorgenetically encoded voltage sensoroptogeneticstwo-photon microscopywavefront shaping

Identifiers

PMID26468193
PMCPMC4604230
OpenAlexW2293817841

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.