Evidence map›Paper›PMID 33864263›Full record

ArticleThe Journal of comparative neurology2021

Upregulation of eIF4E, but not other translation initiation factors, in dendritic spines during memory formation.

Sofya Gindina, Benjamin Botsford, Kiriana Cowansage, Joseph LeDoux, Eric Klann, Charles Hoeffer, Linnaea Ostroff

Open access · greenAbstract read
In one paragraph

Article in The Journal of comparative neurology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.4field-weighted citation impact, top 21% 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

11 citing papers in PubMed, 16 citations in OpenAlex.

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  8. Rehydration of Freeze Substituted Brain Tissue for Pre-embedding Immunoelectron Microscopy.Microscopy and microanalysis : the official journal of Microscopy Society of America, Microbeam Analysis Society, Microscopical Society of Canada · 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 5 institutions in 1 country.

Sofya GindinaDepartment of Cell Biology, SUNY Downstate Medical Center, Brooklyn, New York, USA.
Benjamin BotsfordCenter for Neural Science, New York University, New York, New York, USA.
Kiriana CowansageCenter for Neural Science, New York University, New York, New York, USA.
Joseph LeDouxCenter for Neural Science, New York University, New York, New York, USA.
Eric KlannCenter for Neural Science, New York University, New York, New York, USA.
Charles HoefferInstitute for Behavioral Genetics, University of Colorado, Boulder, Colorado, USA.
Linnaea OstroffDepartment of Physiology and Neurobiology, University of Connecticut, Storrs, Connecticut, USA.ORCID 0000-0002-3348-342X
New York University · USNathan Kline Institute for Psychiatric Research · USSUNY Downstate Health Sciences University · USUniversity of Colorado Boulder · USUniversity of Connecticut · US

Funding

Translation Regulation in Hippocampal LTP and LTDR01NS047384 · NINDS · NEW YORK UNIVERSITY · PI KLANN, ERIC · 2005 to 2020
$5.2M
Sleep Disruption and Alzheimer's Disease PathologyRF1AG064465 · NIA · UNIVERSITY OF COLORADO · PI HOEFFER, CHARLES A, LINK, CHRISTOPHER D. · 2019 to 2022
$4.4M
Reactive Oxygen Species Signaling in the HippocampusR01NS034007 · NINDS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI KLANN, ERIC · 2000 to 2012
$4.2M
eIF2alpha Phosphorylation in Synaptic Plasticity, Memory, and Brain DisordersR37NS034007 · NINDS · NEW YORK UNIVERSITY · PI KLANN, ERIC · 2014 to 2020
$3.3M
Akt regulation of synaptic plasticity and behaviorR01NS086933 · NINDS · UNIVERSITY OF COLORADO · PI HOEFFER, CHARLES A · 2015 to 2019
$1.8M
Methods for serially multiplexed labeling in EM reconstructions of brain tissueR21MH119517 · NIMH · UNIVERSITY OF CONNECTICUT STORRS · PI OSTROFF, LINNAEA E · 2019 to 2020
$442k
Development of genetically encoded neural tracers for electron microscopyR21MH094965 · NIMH · NEW YORK UNIVERSITY · PI OSTROFF, LINNAEA E · 2011 to 2012
$383k
Synaptic tagging in the lateral amygdala fear conditioning circuitF32MH083583 · NIMH · NEW YORK UNIVERSITY · PI OSTROFF, LINNAEA E · 2008 to 2010
$160k
OXIDATIVE ACTIVATION OF PKC DURING INDUCTION OF LTPR29NS034007 · NINDS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI KLANN, ERIC · 1995 to 1999
–
NIMH NIH HHS F32 MH083583NIMH NIH HHS MH083583NIMH NIH HHS MH094965NIMH NIH HHS MH119517NIMH NIH HHS R21 MH094965NIMH NIH HHS R21 MH119517NINDS NIH HHS NS034007NINDS NIH HHS NS047384NINDS NIH HHS R01 NS034007NINDS NIH HHS R01 NS047384NINDS NIH HHS R01 NS086933NINDS NIH HHS R29 NS034007NINDS NIH HHS R37 NS034007
6 · The paper itself

Abstract

Local translation can provide a rapid, spatially targeted supply of new proteins in distal dendrites to support synaptic changes that underlie learning. Learning and memory are especially sensitive to manipulations of translational control mechanisms, particularly those that target the initiation step, and translation initiation at synapses could be a means of maintaining synapse specificity during plasticity. Initiation predominantly occurs via recruitment of ribosomes to the 5' mRNA cap by complexes of eukaryotic initiation factors (eIFs), and the interaction between eIF4E and eIF4G1 is a particularly important target of translational control pathways. Pharmacological inhibition of eIF4E-eIF4G1 binding impairs formation of memory for aversive Pavlovian conditioning as well as the accompanying increase in polyribosomes in the heads of dendritic spines in the lateral amygdala (LA). This is consistent with a role for initiation at synapses in memory formation, but whether eIFs are even present near synapses is unknown. To determine whether dendritic spines contain eIFs and whether eIF distribution is affected by learning, we combined immunolabeling with serial section transmission electron microscopy (ssTEM) volume reconstructions of LA dendrites after Pavlovian conditioning. Labeling for eIF4E, eIF4G1, and eIF2α-another key target of regulation-occurred in roughly half of dendritic spines, but learning effects were only found for eIF4E, which was upregulated in the heads of dendritic spines. Our results support the possibility of regulated translation initiation as a means of synapse-specific protein targeting during learning and are consistent with the model of eIF4E availability as a central point of control.

Indexed as

AnimalsDendritic SpinesEukaryotic Initiation Factor-4EEukaryotic Initiation FactorsMaleMemoryProtein BiosynthesisRatsRats, Sprague-DawleyUp-RegulationEukaryotic Initiation Factor-4EEukaryotic Initiation Factorsamygdaladendritic spineelectron microscopyeukaryotic initiation factorfear conditioninglearning and memorypolyribosome

Identifiers

PMID33864263
PMCPMC8165027
OpenAlexW3154051819

What OpenQuestion holds

Textmetadata
LicenceTDM
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.