Evidence map›Paper›PMID 18084300›Full record

ArticleNature methods2008

Tracking transmitter-gated P2X cation channel activation in vitro and in vivo.

Esther Richler, Severine Chaumont, Eiji Shigetomi, Alvaro Sagasti, Baljit S Khakh

Abstract read
In one paragraph

Article in Nature methods, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

30 citing papers in PubMed, 47 citations in OpenAlex.

  1. Review
  2. Review
  3. Photoswitching alters fluorescence readout of jGCaMP8 CaProceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  4. Review
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  8. Review
  9. Genetically targeted single-channel optical recording reveals multiple Orai1 gating states and oscillations in calcium influx.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Detection of endogenous substances with enzymatic microelectrode biosensors in the kidney.American journal of physiology. Regulatory, integrative and comparative physiology · 2013
    Review
  15. Review
  16. Article
  17. P2X2 and P2X5 subunits define a new heteromeric receptor with P2X7-like properties.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2012
    Article
  18. Article
  19. Neuronal P2X2 receptors are mobile ATP sensors that explore the plasma membrane when activated.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2011
    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

5 authors at 1 institution in 1 country.

Esther RichlerDepartment of Physiology, University of California Los Angeles, 10833 LeConte Avenue, Los Angeles, California 90095, USA.
Severine Chaumont
Eiji Shigetomi
Alvaro Sagasti
Baljit S Khakh
University of California, Los Angeles · US

Funding

Training in Molecular, Cellular &Integrative PhysiologyT32GM065823 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI TIDBALL, JAMES G · 2003 to 2017
$2.1M
P2X channel mobility in the plasma membrane of neuronsF31NS064794 · NINDS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI RICHLER, ESTHER · 2009 to 2011
$63k
NIGMS NIH HHS T32 GM065823NINDS NIH HHS F31 NS064794Wellcome Trust
6 · The paper itself

Abstract

We present a noninvasive approach to track activation of ATP-gated P2X receptors and potentially other transmitter-gated cation channels that show calcium fluxes. We genetically engineered rat P2X receptors to carry calcium sensors near the channel pore and tested this as a reporter for P2X(2) receptor opening. The method has several advantages over previous attempts to image P2X channel activation by fluorescence resonance energy transfer (FRET): notably, it reports channel opening rather than a conformation change in the receptor protein. Our FRET-based imaging approach can be used as a general method to track, in real time, the location, regional expression variation, mobility and activation of transmitter-gated P2X channels in living neurons in vitro and in vivo. This approach should help to determine when, where and how different receptors are activated during physiological processes.

Indexed as

CalciumFluorescence Resonance Energy TransferIon Channel GatingNeuronsReceptors, Purinergic P2Receptors, Purinergic P2XCalciumReceptors, Purinergic P2Receptors, Purinergic P2X

Identifiers

PMID18084300
PMCPMC3523716
OpenAlexW1980499424

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.