Evidence map›Paper›PMID 28300646›Full record

ArticleMolecular and cellular neurosciences2017

Developmental changes in trak-mediated mitochondrial transport in neurons.

Omar Loss, F Anne Stephenson

Open access · hybridAbstract read
In one paragraph

Article in Molecular and cellular neurosciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

21 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
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  5. Article
  6. Review
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  10. Mitochondria as central hubs in synaptic modulation.Cellular and molecular life sciences : CMLS · 2023
    Review
  11. Review
  12. Article
  13. Review
  14. Review
  15. Quantitative Imaging of BiochemistryACS central science · 2020
    Review
  16. Article
  17. Review
  18. Article
  19. Axonal Transport and Mitochondrial Function in Neurons.Frontiers in cellular neuroscience · 2019
    Review
  20. 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

2 authors at 1 institution in 1 country.

Omar LossSchool of Pharmacy University College London, 29/39 Brunswick Square, London WC1N 1AX, United Kingdom.
F Anne StephensonSchool of Pharmacy University College London, 29/39 Brunswick Square, London WC1N 1AX, United Kingdom. Electronic address: anne.stephenson@ucl.ac.uk.
University College London · GB

Funding

Biotechnology and Biological Sciences Research Council BB/K014285/1
6 · The paper itself

Abstract

Previous studies established that the kinesin adaptor proteins, TRAK1 and TRAK2, play an important role in mitochondrial transport in neurons. They link mitochondria to kinesin motor proteins via a TRAK acceptor protein in the mitochondrial outer membrane, the Rho GTPase, Miro. TRAKs also associate with enzyme, O-linked N-acetylglucosamine transferase (OGT), to form a quaternary, mitochondrial trafficking complex. A recent report suggested that TRAK1 preferentially controls mitochondrial transport in axons of hippocampal neurons whereas TRAK2 controls mitochondrial transport in dendrites. However, it is not clear whether the function of any of these proteins is exclusive to axons or dendrites and if their mechanisms of action are conserved between different neuronal populations and also, during maturation. Here, a comparative study was carried out into TRAK-mediated mitochondrial mobility in axons and dendrites of hippocampal and cortical neurons during maturation in vitro using a shRNA gene knockdown approach. It was found that in mature hippocampal and cortical neurons, TRAK1 predominantly mediates axonal mitochondrial transport whereas dendritic transport is mediated via TRAK2. In young, maturing neurons, TRAK1 and TRAK2 contribute similarly in mitochondrial transport in both axons and dendrites in both neuronal types. These findings demonstrate maturation regulation of mitochondrial transport which is conserved between at least two distinct neuronal subtypes.

Indexed as

Adaptor Proteins, Vesicular TransportAnimalsAxonal TransportCarrier ProteinsCells, CulturedCerebral CortexDendritesDisks Large Homolog 4 ProteinHippocampusHumansIntracellular Signaling Peptides and ProteinsMembrane ProteinsMicroscopy, ConfocalMitochondriaN-AcetylglucosaminyltransferasesNerve Tissue ProteinsAdaptor Proteins, Vesicular TransportCarrier ProteinsDisks Large Homolog 4 ProteinDlg4 protein, ratIntracellular Signaling Peptides and ProteinsMembrane ProteinsN-AcetylglucosaminyltransferasesNerve Tissue ProteinsRNA, Small InterferingSynaptophysintau ProteinsTRAK1 protein, humanTRAK2 protein, humanUDP-N-acetylglucosamine-peptide beta-N-acetylglucosaminyltransferaseAxonal transportKinesinMitochondrial transportTrafficking kinesin binding proteinTRAK

Identifiers

PMID28300646
PMCPMC5400476
OpenAlexW2592879598

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.