Evidence map›Paper›PMID 26500494›Full record

ArticleFrontiers in cellular neuroscience2015

Vesicular expression and release of ATP from dopaminergic neurons of the mouse retina and midbrain.

Tracy Ho, Andrew I Jobling, Ursula Greferath, Trinette Chuang, Archana Ramesh, Erica L Fletcher, Kirstan A Vessey

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cellular neuroscience, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
5.0field-weighted citation impact, top 5% 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

26 citing papers in PubMed, 54 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Review
  6. P2XFEBS open bio · 2022
    Article
  7. Article
  8. Stable expression of the human dopamine transporter in N27 cells as an in vitro model for dopamine cell trafficking and metabolism.Toxicology in vitro : an international journal published in association with BIBRA · 2021
    Article
  9. Review
  10. Article
  11. Review
  12. Neonatal Seizures and Purinergic Signalling.International journal of molecular sciences · 2020
    Review
  13. Article
  14. Article
  15. Review
  16. Effects of adenosine APsychopharmacology · 2019
    Article
  17. Review
  18. Review
  19. P2YMolecular neurobiology · 2018
    Article
  20. 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

7 authors at 2 institutions in 2 countries.

Tracy HoVisual Neuroscience Laboratory, Department of Anatomy and Neuroscience, The University of Melbourne Parkville, VIC, Australia.
Andrew I JoblingVisual Neuroscience Laboratory, Department of Anatomy and Neuroscience, The University of Melbourne Parkville, VIC, Australia.
Ursula GreferathVisual Neuroscience Laboratory, Department of Anatomy and Neuroscience, The University of Melbourne Parkville, VIC, Australia.
Trinette ChuangPolyclonal Antibody Development, R&D Antibody Development, EMD Millipore Temecula, CA, USA.
Archana RameshPolyclonal Antibody Development, R&D Antibody Development, EMD Millipore Temecula, CA, USA.
Erica L FletcherVisual Neuroscience Laboratory, Department of Anatomy and Neuroscience, The University of Melbourne Parkville, VIC, Australia.
Kirstan A VesseyVisual Neuroscience Laboratory, Department of Anatomy and Neuroscience, The University of Melbourne Parkville, VIC, Australia.
University of Melbourne · AUInterDigital (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Vesicular nucleotide transporter (VNUT) is required for active accumulation of adenosine tri-phosphate (ATP) into vesicles for purinergic neurotransmission, however, the cell types that express VNUT in the central nervous system remain unknown. This study characterized VNUT expression within the mammalian retina and brain and assessed a possible functional role in purinergic signaling. Two native isoforms of VNUT were detected in mouse retina and brain based on RNA transcript and protein analysis. Using immunohistochemistry, VNUT was found to co-localize with tyrosine hydroxylase (TH) positive, dopaminergic (DA) neurons of the substantia nigra and ventral tegmental area, however, VNUT expression in extranigral non-DA neurons was also observed. In the retina, VNUT labeling was found to co-localize solely with TH-positive DA-cells. In the outer retina, VNUT-positive interplexiform cell processes were in close contact with horizontal cells and cone photoreceptor terminals, which are known to express P2 purinergic-receptors. In order to assess function, dissociated retinal neurons were loaded with fluorescent ATP markers (Quinacrine or Mant-ATP) and the DA marker FFN102, co-labeled with a VNUT antibody and imaged in real time. Fluorescent ATP markers and FFN102 puncta were found to co-localize in VNUT positive neurons and upon stimulation with high potassium, ATP marker fluorescence at the cell membrane was reduced. This response was blocked in the presence of cadmium. These data suggest DA neurons co-release ATP via calcium dependent exocytosis and in the retina this may modulate the visual response by activating purine receptors on closely associated neurons.

Indexed as

dopamineextracellular adenosine tri-phosphate (eATP)purinergicretinal neuronsSLC17A9substantia nigraventral tegmental area (VTA)vesicular nucleotide transporter (VNUT)

Identifiers

PMID26500494
PMCPMC4593860
OpenAlexW1836457398

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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.