Evidence map›Paper›PMID 23612789›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2013

Differential targeting of the dopamine transporter to recycling or degradative pathways during amphetamine- or PKC-regulated endocytosis in dopamine neurons.

Weimin C Hong, Susan G Amara

Open access · greenAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2013. 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
2.3field-weighted citation impact, top 13% 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, 66 citations in OpenAlex.

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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

2 authors at 1 institution in 1 country.

Weimin C HongDepartment of Neurobiology, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Susan G Amara
University of Pittsburgh · US

Funding

Structure, Function and Pharmacology of Neurotransmitter Reuptake SystemsZIAMH002946 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI AMARA, SUSAN · 2013 to 2025
$26.6M
MOLECULAR STUDIES OF CATECHOLAMINE TRANSPORTERSR37DA007595 · NIDA · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI AMARA, SUSAN G. · 1997 to 2006
$1.3M
MOLECULAR STUDIES OF CATECHOLAMINE TRANSPORTERSR01DA007595 · NIDA · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI AMARA, SUSAN G. · 1992 to 2010
$758k
NIDA NIH HHS DA07595NIDA NIH HHS R01 DA007595NIDA NIH HHS R37 DA007595
6 · The paper itself

Abstract

The dopamine transporter (DAT) clears the extracellular dopamine released during neurotransmission and is a major target for both therapeutic and addictive psychostimulant amphetamines. Amphetamine exposure or activation of protein kinase C (PKC) by the phorbol ester PMA has been shown to down-regulate cell surface DAT. However, in dopamine neurons, the trafficking itinerary and fate of internalized DAT has not been elucidated. By monitoring surface-labeled DAT in transfected dopamine neurons from embryonic rat mesencephalic cultures, we find distinct sorting and fates of internalized DAT after amphetamine or PMA treatment. Although both drugs promote DAT internalization above constitutive endocytosis in dopamine neurons, PMA induces ubiquitination of DAT and leads to accumulation of DAT on LAMP1-positive endosomes. In contrast, after amphetamine exposure DAT is sorted to recycling endosomes positive for Rab11 and the transferrin receptor. Furthermore, quantitative assessment of DAT recycling using an antibody-feeding assay reveals that significantly less DAT returns to the surface of dopamine neurons after internalization by PMA, compared with vehicle or amphetamine treatment. These results demonstrate that, in neurons, the DAT is sorted differentially to recycling and degradative pathways after psychostimulant exposure or PKC activation, which may allow for either the transient or sustained inhibition of DAT during dopamine neurotransmission.

Indexed as

AmphetamineAnimalsCell LineCells, CulturedDopamineDopamine AgentsDopamine Plasma Membrane Transport ProteinsDopaminergic NeuronsEndocytosisEndosomesEnzyme ActivationHEK293 CellsHumansLuminescent ProteinsLysosomal-Associated Membrane Protein 1Microscopy, ConfocalAmphetamineDopamineDopamine AgentsDopamine Plasma Membrane Transport ProteinsLuminescent ProteinsLysosomal-Associated Membrane Protein 1Protein Kinase Crab11 GTP-Binding Proteinsrab GTP-Binding ProteinsReceptors, TransferrinTetradecanoylphorbol Acetateendosome sortingfluorescence imaginginternalizationubiquitination

Identifiers

PMID23612789
PMCPMC3714572
OpenAlexW2097580689

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.