Evidence map›Paper›PMID 18096700›Full record

ArticleThe Journal of biological chemistry2008

Reticulon RTN2B regulates trafficking and function of neuronal glutamate transporter EAAC1.

Yiting Liu, Svetlana Vidensky, Alicia M Ruggiero, Susanne Maier, Harald H Sitte, Jeffrey D Rothstein

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
1.7field-weighted citation impact, top 18% 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

37 citing papers in PubMed, 65 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

6 authors at 3 institutions in 2 countries.

Yiting LiuDepartments of Neurology and Neuroscience, School of Medicine, Johns Hopkins University, Baltimore, MD 21287, USA.
Svetlana Vidensky
Alicia M Ruggiero
Susanne Maier
Harald H Sitte
Jeffrey D Rothstein
Johns Hopkins Medicine · USMedical University of Vienna · ATJohns Hopkins University · US

Funding

Neuronal vs. glial glutamate transport regulation in ALSR01NS033958 · NINDS · JOHNS HOPKINS UNIVERSITY · PI ROTHSTEIN, JEFFREY D · 1995 to 2013
$5.4M
Therapeutic Expression of Glial Glutamate TransportersR01NS052179 · NINDS · JOHNS HOPKINS UNIVERSITY · PI ROTHSTEIN, JEFFREY D · 2005 to 2009
$1.8M
NEURONAL GLUTAMATE TRANSPORTER ASSOCIATED PROTEINS(GTRAPR01NS040151 · NINDS · JOHNS HOPKINS UNIVERSITY · PI ROTHSTEIN, JEFFREY D · 2000 to 2004
$1.5M
Characterizing Beta Lactams/Neuroprotective Drugs/ALSU01NS050094 · NINDS · JOHNS HOPKINS UNIVERSITY · PI ROTHSTEIN, JEFFREY D · 2005 to 2010
$1.1M
Austrian Science Fund FWF P 18706NINDS NIH HHS NS 33958NINDS NIH HHS NS 40151NINDS NIH HHS NS 52179NINDS NIH HHS R01 NS033958NINDS NIH HHS R01 NS040151NINDS NIH HHS R01 NS052179NINDS NIH HHS U01 NS050094
6 · The paper itself

Abstract

Excitatory amino acid transporters (EAATs) are the primary regulators of extracellular glutamate concentrations in the central nervous system. Their dysfunction may contribute to several neurological diseases. To date, five distinct mammalian glutamate transporters have been cloned. In brain, EAAC1 (excitatory amino acid carrier 1) is the primary neuronal glutamate transporter, localized on the perisynaptic membranes that are near release sites. Despite its potential importance in synaptic actions, little is known concerning the regulation of EAAC1 trafficking from the endoplasmic reticulum (ER) to the cell surface. Previously, we identified an EAAC1-associated protein, GTRAP3-18, an ER protein that prevents ER exit of EAAC1 when induced. Here we show that RTN2B, a member of the reticulon protein family that mainly localizes in the ER and ER exit sites interacts with EAAC1 and GTRAP3-18. EAAC1 and GTRAP3-18 bind to different regions of RTN2B. Each protein can separately and independently form complexes with EAAC1. RTN2B enhances ER exit and the cell surface composition of EAAC1 in heterologous cells. Expression of short interfering RNA-mediated knockdown of RTN2B decreases the EAAC1 protein level in neurons. Overall, our results suggest that RTN2B functions as a positive regulator in the delivery of EAAC1 from the ER to the cell surface. These studies indicate that transporter exit from the ER controlled by the interaction with its ER binding partner represents a critical regulatory step in glutamate transporter trafficking to the cell surface.

Indexed as

AnimalsBrainChlorocebus aethiopsCOS CellsEndoplasmic ReticulumExcitatory Amino Acid Transporter 3Glutamic AcidHumansMembrane ProteinsMiceMuscle ProteinsNerve Tissue ProteinsNeuronsProtein TransportRatsRNA, Small InterferingExcitatory Amino Acid Transporter 3Glutamic AcidMembrane ProteinsMuscle ProteinsNerve Tissue ProteinsRNA, Small InterferingRTN2 protein, humanSLC1A1 protein, humanSlc1a1 protein, rat

Identifiers

PMID18096700
PMCPMC2581797
OpenAlexW2036064501

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.