Evidence map›Paper›PMID 31545171›Full record

ArticleeLife2019

Optical dopamine monitoring with dLight1 reveals mesolimbic phenotypes in a mouse model of neurofibromatosis type 1.

J Elliott Robinson, Gerard M Coughlin, Acacia M Hori, Jounhong Ryan Cho, Elisha D Mackey, Zeynep Turan, Tommaso Patriarchi, Lin Tian, Viviana Gradinaru

Open access · goldAbstract read
In one paragraph

Article in eLife, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
4.1field-weighted citation impact, top 6% 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

30 citing papers in PubMed, 48 citations in OpenAlex.

  1. Trial
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  3. Tail-rattling in rodents: more than a threat display.Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology · 2026
    Review
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  20. Structural basis of receptor usage by the engineered capsid AAV-PHP.eB.Molecular therapy. Methods & clinical development · 2022
    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

9 authors at 2 institutions in 1 country.

J Elliott RobinsonDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, United States.ORCID https://orcid.org/0000-0001-9417-3938
Gerard M CoughlinDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, United States.
Acacia M HoriDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, United States.
Jounhong Ryan ChoDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, United States.
Elisha D MackeyDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, United States.
Zeynep TuranDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, United States.
Tommaso PatriarchiDepartment of Biochemistry and Molecular Medicine, University of California, Davis, Davis, United States.
Lin TianDepartment of Biochemistry and Molecular Medicine, University of California, Davis, Davis, United States.ORCID http://orcid.org/0000-0001-7012-6926
Viviana GradinaruDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, United States.ORCID https://orcid.org/0000-0001-5868-348X
California Institute of Technology · USUniversity of California, Davis · US

Funding

Genetically encoded indicators for large-scale sensing of neuromodulatory signaling in behaving animalsU01NS103522 · NINDS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI NIMMERJAHN, AXEL, TIAN, LIN · 2017 to 2019
$2.9M
Fluorescent biosensors for imaging neurotransmitters: observing synapses in actioDP2MH107056 · NIMH · UNIVERSITY OF CALIFORNIA AT DAVIS · PI TIAN, LIN · 2014 to 2014
$2.3M
Noninvasive Gene Delivery for Monitoring and Perturbing Cell Types and Circuits in Transgenic and Non-Transgenic AnimalsRF1MH117069 · NIMH · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI GRADINARU, VIVIANA · 2018 to 2018
$2.3M
NIH HHS DP2MH107056NIH HHS IDP20D017782-01NIH HHS PECASENIH HHS RF1MH117069NIH HHS U01NS103522NIMH NIH HHS DP2 MH107056NIMH NIH HHS RF1 MH117069NINDS NIH HHS U01 NS103522
6 · The paper itself

Abstract

Neurofibromatosis type 1 (NF1) is an autosomal dominant disorder whose neurodevelopmental symptoms include impaired executive function, attention, and spatial learning and could be due to perturbed mesolimbic dopaminergic circuitry. However, these circuits have never been directly assayed in vivo. We employed the genetically encoded optical dopamine sensor dLight1 to monitor dopaminergic neurotransmission in the ventral striatum of NF1 mice during motivated behavior. Additionally, we developed novel systemic AAV vectors to facilitate morphological reconstruction of dopaminergic populations in cleared tissue. We found that NF1 mice exhibit reduced spontaneous dopaminergic neurotransmission that was associated with excitation/inhibition imbalance in the ventral tegmental area and abnormal neuronal morphology. NF1 mice also had more robust dopaminergic and behavioral responses to salient visual stimuli, which were independent of learning, and rescued by optogenetic inhibition of non-dopaminergic neurons in the VTA. Overall, these studies provide a first in vivo characterization of dopaminergic circuit function in the context of NF1 and reveal novel pathophysiological mechanisms.

Indexed as

Synaptic TransmissionAnimalsDisease Models, AnimalDopaminergic NeuronsMiceNerve NetNeurofibromatosis 1PhenotypeVentral StriatumAAVdopaminemotivationmouseneurofibromatosisneurosciencerewardtissue clearing

Identifiers

PMID31545171
PMCPMC6819083
OpenAlexW2974570729

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.