Evidence map›Paper›PMID 29649542›Full record

ReviewMolecular and cellular neurosciences2018

New approaches for solving old problems in neuronal protein trafficking.

Ashley M Bourke, Aaron B Bowen, Matthew J Kennedy

Abstract readReview
In one paragraph

Review in Molecular and cellular neurosciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
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

13 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Spatial and Temporal Control of Protein Secretion with Light.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  6. Article
  7. Article
  8. Peptidylglycine α-amidating monooxygenase is required for atrial secretory granule formation.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  9. Architecture and Dynamics of the Neuronal Secretory Network.Annual review of cell and developmental biology · 2019
    Review
  10. A New Look at the Functional Organization of the Golgi Ribbon.Frontiers in cell and developmental biology · 2019
    Article
  11. Article
  12. Review
  13. Article
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

3 authors.

Ashley M BourkeDepartment of Pharmacology, University of Colorado School of Medicine, Aurora, CO, United States.
Aaron B BowenDepartment of Pharmacology, University of Colorado School of Medicine, Aurora, CO, United States.
Matthew J KennedyDepartment of Pharmacology, University of Colorado School of Medicine, Aurora, CO, United States. Electronic address: matthew.kennedy@ucdenver.edu.

Funding

ZEBRAFISH TRANSGENIC CORE - ROCKY MOUNTAIN NEUROLOGICAL DISORDERS CORE CENTERP30NS048154 · NINDS · UNIVERSITY OF COLORADO DENVER · PI RIBERA, ANGELES BADELL · 2004 to 2020
$10.1M
PREDOCTORAL TRAINING PROGRAM IN PHARMACOLOGYT32GM007635 · NIGMS · UNIVERSITY OF COLORADO DENVER · PI DELL'ACQUA, MARK L · 1985 to 2023
$6.1M
Mechanisms of dendritic exocytosisR01NS082271 · NINDS · UNIVERSITY OF COLORADO DENVER · PI KENNEDY, MATTHEW J · 2013 to 2017
$1.7M
Optical tools for extended neural silencingR21EY026363 · NEI · UNIVERSITY OF COLORADO DENVER · PI KENNEDY, MATTHEW J, TUCKER, CHANDRA L · 2015 to 2016
$464k
Mechanisms of beta-amyloid induced synaptic dysfunctionR21AG058005 · NIA · UNIVERSITY OF COLORADO DENVER · PI KENNEDY, MATTHEW J · 2018 to 2019
$423k
Dynamic Control of Local Synaptic-Membrane Protein Composition by the Dendritic Secretory PathwayF30NS092421 · NINDS · UNIVERSITY OF COLORADO DENVER · PI BOWEN, AARON · 2015 to 2018
$128k
Howard Hughes Medical InstituteNEI NIH HHS R21 EY026363NIA NIH HHS R21 AG058005NIGMS NIH HHS T32 GM007635NINDS NIH HHS F30 NS092421NINDS NIH HHS P30 NS048154NINDS NIH HHS R01 NS082271
6 · The paper itself

Abstract

Fundamental cellular properties are determined by the repertoire and abundance of proteins displayed on the cell surface. As such, the trafficking mechanisms for establishing and maintaining the surface proteome must be tightly regulated for cells to respond appropriately to extracellular cues, yet plastic enough to adapt to ever-changing environments. Not only are the identity and abundance of surface proteins critical, but in many cases, their regulated spatial positioning within surface nanodomains can greatly impact their function. In the context of neuronal cell biology, surface levels and positioning of ion channels and neurotransmitter receptors play essential roles in establishing important properties, including cellular excitability and synaptic strength. Here we review our current understanding of the trafficking pathways that control the abundance and localization of proteins important for synaptic function and plasticity, as well as recent technological advances that are allowing the field to investigate protein trafficking with increasing spatiotemporal precision.

Indexed as

Axonal TransportAnimalsHumansNeuronsOptical ImagingReceptors, NeurotransmitterReceptors, NeurotransmitterAMPA receptorDendriteMembrane traffickingOptogeneticsPlasticitySynapse

Identifiers

PMID29649542
PMCPMC6128763

What OpenQuestion holds

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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.