Evidence map›Paper›PMID 30774584›Full record

ArticleFrontiers in neural circuits2019

Two eARCHT3.0 Lines for Optogenetic Silencing of Dopaminergic and Serotonergic Neurons.

Alexandra Krol, Violeta G Lopez-Huerta, Taylor E C Corey, Karl Deisseroth, Jonathan T Ting, Guoping Feng

Open access · goldAbstract read
In one paragraph

Article in Frontiers in neural circuits, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 48% 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

4 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
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

6 authors at 4 institutions in 2 countries.

Alexandra KrolMcGovern Institute for Brain Research, Department of Brain and Cognitive Sciences, Massachusetts Institute of Technology, Cambridge, MA, United States.
Violeta G Lopez-HuertaMcGovern Institute for Brain Research, Department of Brain and Cognitive Sciences, Massachusetts Institute of Technology, Cambridge, MA, United States.
Taylor E C CoreyMcGovern Institute for Brain Research, Department of Brain and Cognitive Sciences, Massachusetts Institute of Technology, Cambridge, MA, United States.
Karl DeisserothDepartment of Bioengineering, Stanford University, Stanford, CA, United States.
Jonathan T TingMcGovern Institute for Brain Research, Department of Brain and Cognitive Sciences, Massachusetts Institute of Technology, Cambridge, MA, United States.
Guoping FengMcGovern Institute for Brain Research, Department of Brain and Cognitive Sciences, Massachusetts Institute of Technology, Cambridge, MA, United States.
McGovern Institute for Brain Research · USAllen Institute for Brain Science · USMassachusetts Institute of Technology · USStanford University · US

Funding

Training CoreP50DA042012 · NIDA · STANFORD UNIVERSITY · PI Karl A. Deisseroth, Lisa Giocomo · 2017 to 2026
$27.1M
CLARITY: fully-assembled biologyR01MH099647 · NIMH · STANFORD UNIVERSITY · PI DEISSEROTH, KARL A. · 2012 to 2016
$23.0M
Dissecting the role of thalamic inhibition in neurodevelopmental diseasesR01NS098505 · NINDS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI FENG, GUOPING, HALASSA, MICHAEL M · 2016 to 2020
$3.2M
Cell Type-Specific Halorhodopsin Mice for Neuronal SilencinR21NS079992 · NINDS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI FENG, GUOPING · 2012 to 2013
$433k
NIDA NIH HHS P50 DA042012NIMH NIH HHS R01 MH099647NINDS NIH HHS R01 NS098505NINDS NIH HHS R21 NS079992
6 · The paper itself

Abstract

Dopaminergic and serotonergic neurons modulate and control processes ranging from reward signaling to regulation of motor outputs. Further, dysfunction of these neurons is involved in both degenerative and psychiatric disorders. Elucidating the roles of these neurons has been greatly facilitated by bacterial artificial chromosome (BAC) transgenic mouse lines expressing channelrhodopsin to readily enable cell-type specific activation. However, corresponding lines to silence these monoaminergic neurons have been lacking. We have generated two BAC transgenic mouse lines expressing the outward proton pump, enhanced ArchT3.0 (eArchT3.0), and GFP under control of the regulatory elements of either the dopamine transporter (DAT; Jax# 031663) or the tryptophan hydroxylase 2 (TPH2; Jax# 031662) gene locus. We demonstrate highly faithful and specific expression of these lines in dopaminergic and serotonergic neurons respectively. Additionally we validate effective and sensitive eArchT3.0-mediated silencing of these neurons using slice electrophysiology as well as with a well-established behavioral assay. These new transgenic tools will help expedite the study of dopaminergic and serotonergic system function in normal behavior and disease.

Indexed as

OptogeneticsAction PotentialsAnimalsBrainChannelrhodopsinsDopamine Plasma Membrane Transport ProteinsDopaminergic NeuronsElectric StimulationGenetic VectorsGreen Fluorescent ProteinsHEK293 CellsHumansIn Vitro TechniquesMiceMice, Inbred C57BLMice, TransgenicChannelrhodopsinsDopamine Plasma Membrane Transport Proteinsenhanced green fluorescent proteinGreen Fluorescent ProteinsRNA, MessengerTph2 protein, mouseTryptophan HydroxylaseTyrosine 3-MonooxygenasedopaminergiceArchT3.0inhibitorymouseopsinserotonergic

Identifiers

PMID30774584
PMCPMC6367884
OpenAlexW2914578145

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.