Evidence map›Paper›PMID 29617653›Full record

ArticleCell reports2018

Removing 4E-BP Enables Synapses to Refine without Postsynaptic Activity.

Yumaine Chong, Natasha Saviuk, Brigitte Pie, Nathan Basisty, Ryan K Quinn, Birgit Schilling, Nahum Sonenberg, Ellis Cooper, A Pejmun Haghighi

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.6field-weighted citation impact, top 38% 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

8 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Calmodulin Triggers Activity-Dependent rRNA Biogenesis via Interaction with DDX21.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  5. Control of Selective mRNA Translation in Neuronal Subcellular Compartments in Health and Disease.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
    Review
  6. Review
  7. Article
  8. Review
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 2 countries.

Yumaine ChongDepartment of Physiology, McGill University, Montreal, QC H3G 1Y6, Canada.
Natasha SaviukDepartment of Physiology, McGill University, Montreal, QC H3G 1Y6, Canada.
Brigitte PieDepartment of Physiology, McGill University, Montreal, QC H3G 1Y6, Canada.
Nathan BasistyBuck Institute for Research on Aging, Novato, CA 94945, USA.
Ryan K QuinnBuck Institute for Research on Aging, Novato, CA 94945, USA.
Birgit SchillingBuck Institute for Research on Aging, Novato, CA 94945, USA.
Nahum SonenbergDepartment of Biochemistry, McGill University, Montreal, QC H3G 1Y6, Canada.
Ellis CooperDepartment of Physiology, McGill University, Montreal, QC H3G 1Y6, Canada. Electronic address: ellis.cooper@mcgill.ca.
A Pejmun HaghighiDepartment of Physiology, McGill University, Montreal, QC H3G 1Y6, Canada; Buck Institute for Research on Aging, Novato, CA 94945, USA. Electronic address: phaghighi@buckinstitute.org.
McGill University · CABuck Institute for Research on Aging · US

Funding

TripleTOF 5600 High Resolution Mass SpectrometerS10OD016281 · OD · BUCK INSTITUTE FOR RESEARCH ON AGING · PI GIBSON, BRADFORD WAYNE · 2013 to 2013
$597k
CIHRNIH HHS S10 OD016281
6 · The paper itself

Abstract

Throughout the developing nervous system, considerable synaptic re-organization takes place as postsynaptic neurons extend dendrites and incoming axons refine their synapses, strengthening some and eliminating others. It is well accepted that these processes rely on synaptic activity; however, the mechanisms that lead to this developmental reorganization are not fully understood. Here, we explore the regulation of cap-dependent translation, a mechanism known to play a role in synaptic growth and plasticity. Using sympathetic ganglia in α3 nicotinic acetylcholine receptor (nAChR)-knockout (KO) mice, we establish that electrophysiologically silent synapses between preganglionic axons and postsynaptic sympathetic neurons do not refine, and the growth of dendrites and the targeting of synapses on postsynaptic neurons are impaired. Remarkably, genetically removing 4E-BP, a suppressor of cap-dependent translation, from these α3 nAChR-KO mice largely restores these features. We conclude that synaptic connections can re-organize and refine without postsynaptic activity during post-natal development when 4E-BP-regulated cap-dependent translation is enhanced.

Indexed as

Synaptic PotentialsAdaptor Proteins, Signal TransducingAnimalsCarrier ProteinsCell Cycle ProteinsEukaryotic Initiation FactorsGanglia, SympatheticMicePhosphoproteinsReceptors, NicotinicSynapsesAdaptor Proteins, Signal TransducingCarrier ProteinsCell Cycle ProteinsEif4ebp1 protein, mouseEukaryotic Initiation FactorsPhosphoproteinsReceptors, Nicotiniccap-dependent translationnicotinic receptorssilent synapsessympathetic neuronssynaptic activitysynaptic refinement

Identifiers

PMID29617653
PMCPMC6483372
OpenAlexW2796223576

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.