Evidence map›Paper›PMID 12972553›Full record

ArticleMolecular biology of the cell2003

Expression of phosphatidylinositol (4,5) bisphosphate-specific pleckstrin homology domains alters direction but not the level of axonal transport of mitochondria.

Kurt J De Vos, Julia Sable, Kyle E Miller, Michael P Sheetz

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

33 citing papers in PubMed, 77 citations in OpenAlex.

  1. Article
  2. Review
  3. The Divergent Roles of Dietary Saturated and Monounsaturated Fatty Acids on Nerve Function in Murine Models of Obesity.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2019
    Article
  4. Article
  5. Dyslipidemia impairs mitochondrial trafficking and function in sensory neurons.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2018
    Article
  6. Review
  7. Article
  8. Review
  9. Mutant β-III spectrin causes mGluR1α mislocalization and functional deficits in a mouse model of spinocerebellar ataxia type 5.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2014
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Lipid signaling on the mitochondrial surface.Biochimica et biophysica acta · 2009
    Review
  20. Mitochondrial transport and docking in axons.Experimental neurology · 2009
    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

4 authors at 1 institution in 1 country.

Kurt J De VosDepartment of Biological Sciences, Columbia University, New York, New York 10027, USA.
Julia Sable
Kyle E Miller
Michael P Sheetz
Columbia University · US

Funding

MOLECULAR BASIS OF ORGANELLE MOVEMENT IN AXONSR01NS023345 · NINDS · WASHINGTON UNIVERSITY · PI SHEETZ, MICHAEL P · 1986 to 2002
$651k
NINDS NIH HHS NS23345
6 · The paper itself

Abstract

Axonal transport of membranous organelles such as mitochondria is essential for neuron viability and function. How signaling mechanisms regulate or influence mitochondrial distribution and transport is still largely unknown. We observed an increase in the distal distribution of mitochondria in neurons upon the expression of pleckstrin homology (PH) domains of phospholipase Cdelta1 (PLCdelta-PH) and spectrin (spectrin-PH). Quantitative analysis of mitochondrial transport showed that specific binding of PH domains to phosphatidylinositol (4,5) bisphosphate (PtdIns(4,5)P2) but not 3' phosphorylated phosphatidylinositol species enhanced plus-end-directed transport of mitochondria two- to threefold and at the same time decreased minus-end-directed transport of mitochondria along axonal microtubules (MTs) without altering the overall level of motility. Further, the velocity and duration of mitochondrial transport plus the association of molecular motors with mitochondria remained unchanged by the expression of PH domains. Thus, PtdIns(4,5)P2-specific PH domains caused an increase in distal mitochondria by disturbing the balance of plus- and minus-end-directed transport rather than directly affecting the molecular machinery involved. Taken together our data reveal that level and directionality of transport are separable and that PtdIns(4,5)P2 has a novel role in regulation of the directionality of axonal transport of mitochondria.

Indexed as

AnimalsAxonal TransportCells, CulturedCloning, MolecularGrowth ConesHumansIsoenzymesMitochondriaPhosphatidylinositol 4,5-DiphosphatePhospholipase C deltaPhosphorylationProtein Structure, TertiarySpectrinType C PhospholipasesIsoenzymesPhosphatidylinositol 4,5-DiphosphatePhospholipase C deltaSpectrinType C Phospholipases

Identifiers

PMID12972553
PMCPMC196556
OpenAlexW2146771791

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.