Evidence map›Paper›PMID 28847807›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2017

The Dopamine Transporter Recycles via a Retromer-Dependent Postendocytic Mechanism: Tracking Studies Using a Novel Fluorophore-Coupling Approach.

Sijia Wu, Rita R Fagan, Chayasith Uttamapinant, Lawrence M Lifshitz, Kevin E Fogarty, Alice Y Ting, Haley E Melikian

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
4.0field-weighted citation impact, top 5% 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

40 citing papers in PubMed, 69 citations in OpenAlex.

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  13. Rit2 silencing in dopamine neurons drives a Parkinsonian phenotype.bioRxiv : the preprint server for biology · 2023
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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

7 authors at 3 institutions in 1 country.

Sijia WuBrudnick Neuropsychiatric Research Institute, University of Massachusetts Medical School, Worcester, Massachusetts 01604.
Rita R FaganBrudnick Neuropsychiatric Research Institute, University of Massachusetts Medical School, Worcester, Massachusetts 01604.ORCID 0000-0002-8600-0364
Chayasith UttamapinantDepartment of Chemistry, Massachusetts Institute of Technology, Cambridge, Massachusetts 02142.
Lawrence M LifshitzBiomedical Imaging Group, Program in Molecular Medicine, University of Massachusetts Medical School, Worcester, Massachusetts 01605, and.ORCID 0000-0001-6197-6638
Kevin E FogartyBiomedical Imaging Group, Program in Molecular Medicine, University of Massachusetts Medical School, Worcester, Massachusetts 01605, and.
Alice Y TingDepartments of Genetics, Biology, and Chemistry, Stanford University, Stanford, California 94305.
Haley E MelikianBrudnick Neuropsychiatric Research Institute, University of Massachusetts Medical School, Worcester, Massachusetts 01604, haley.melikian@umassmed.edu.ORCID 0000-0002-9694-5556
University of Massachusetts Chan Medical School · USMassachusetts Institute of Technology · USStanford University · US

Funding

Trafficking and Regulation of Monoamine TransportersR01DA015169 · NIDA · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI MELIKIAN, HALEY E · 2002 to 2017
$5.2M
Dopamine Transporter Cell Surface DynamicsR01DA035224 · NIDA · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI MELIKIAN, HALEY E · 2013 to 2022
$4.3M
NIDA NIH HHS R01 DA015169NIDA NIH HHS R01 DA035224
6 · The paper itself

Abstract

Presynaptic reuptake, mediated by the dopamine (DA) transporter (DAT), terminates DAergic neurotransmission and constrains extracellular DA levels. Addictive and therapeutic psychostimulants inhibit DA reuptake and multiple DAT coding variants have been reported in patients with neuropsychiatric disorders. These findings underscore that DAT is critical for DA neurotransmission and homeostasis. DAT surface availability is regulated acutely by endocytic trafficking, and considerable effort has been directed toward understanding mechanisms that govern DAT's plasma membrane expression and postendocytic fate. Multiple studies have demonstrated DAT endocytic recycling and enhanced surface delivery in response to various stimuli. Paradoxically, imaging studies have not detected DAT targeting to classic recycling endosomes, suggesting that internalized DAT targets to either degradation or an undefined recycling compartment. Here, we leveraged PRIME (

Indexed as

EndocytosisAnimalsCell MembraneDopamine Plasma Membrane Transport ProteinsEndosomesHEK293 CellsHumansMaleMesencephalonMiceMice, Inbred C57BLNeuronsPresynaptic TerminalsProtein Sorting SignalsProtein TransportRatsDopamine Plasma Membrane Transport ProteinsProtein Sorting Signalscocainedopamineendocytosisretromerreuptaketrafficking

Identifiers

PMID28847807
PMCPMC5618262
OpenAlexW2747981361

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.