Evidence map›Paper›PMID 11136854›Full record

ArticleThe Journal of physiology2001

Regulation of Drosophila transient receptor potential-like (TrpL) channels by phospholipase C-dependent mechanisms.

M Estacion, W G Sinkins, W P Schilling

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of physiology, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
4.1field-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

52 citing papers in PubMed, 134 citations in OpenAlex.

  1. Article
  2. Diacylglycerol Activates theInternational journal of molecular sciences · 2023
    Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Phosphoinositide regulation of TRPV1 revisited.Pflugers Archiv : European journal of physiology · 2015
    Review
  9. Article
  10. Diacylglycerol activates the light-dependent channel TRP in the photosensitive microvilli of Drosophila melanogaster photoreceptors.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2014
    Article
  11. Phosphoinositide regulation of TRP channels.Handbook of experimental pharmacology · 2014
    Review
  12. Review
  13. Review
  14. Article
  15. Article
  16. TRPC5 channel is the mediator of neurotrophin-3 in regulating dendritic growth via CaMKIIα in rat hippocampal neurons.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2012
    Article
  17. Drosophila visual transduction.Trends in neurosciences · 2012
    Review
  18. Article
  19. Article
  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

3 authors at 1 institution in 1 country.

M EstacionRammelkamp Center for Education and Research, MetroHealth Medical Center and the Department of Physiology and Biophysics, Case Western Reserve University School of Medicine, Cleveland, OH 44109, USA.
W G Sinkins
W P Schilling
Case Western Reserve University · US

Funding

CALCIUM CHANNELS IN NONEXCITABLE CELLSR01GM052019 · NIGMS · CASE WESTERN RESERVE UNIVERSITY · PI SCHILLING, WILLIAM P · 1995 to 2006
$2.5M
NIGMS NIH HHS GM52019NIGMS NIH HHS R01 GM052019
6 · The paper itself

Abstract

Patch clamp and fura-2 fluorescence were employed to characterize receptor-mediated activation of recombinant Drosophila TrpL channels expressed in Sf9 insect cells. TrpL was activated by receptor stimulation and by exogenous application of diacylglycerol (DAG) or poly-unsaturated fatty acids (PUFAs). Activation of TrpL was blocked more than 70% by U73122, suggesting that the effect of these agents was dependent upon phospholipase C (PLC). In fura-2 assays, extracellular application of bacterial phosphatidylinositol (PI)-PLC or phosphatidylcholine (PC)-PLC caused a transient increase in TrpL channel activity, the magnitude of which was significantly less than that observed following receptor stimulation. TrpL channels were also activated in excised inside-out patches by cytoplasmic application of mammalian PLC-b2, bacterial PI-PLC and PC-PLC, but not by phospholipase D (PLD). The phospholipases had little or no effect when examined in either whole-cell or cell-attached configurations.TrpL activity was inhibited by addition of phosphatidylinositol-4,5-bisphosphate (PIP2) to excised inside-out membrane patches exhibiting spontaneous channel activity or to patches pre-activated by treatment with PLC. The effect was reversible, specific for PIP2, and was not observed with phosphatidylethanolamine (PE), PI, PC or phosphatidylserine (PS). However, antibodies against PIP2 consistently failed to activate TrpL in inside-out patches. It is concluded that both the hydrolysis of PIP2 and the generation of DAG are required to rapidly activate TrpL following receptor stimulation, or that some other PLC-dependent mechanism plays a crucial role in the activation process.

Indexed as

Drosophila ProteinsAnimalsBaculoviridaeCalciumCalmodulin-Binding ProteinsCell LineCHO CellsCricetinaeDrosophilaFluorescent DyesFura-2Indicators and ReagentsMembrane PotentialsMembrane ProteinsOocytesPatch-Clamp TechniquesCalciumCalmodulin-Binding ProteinsDrosophila ProteinsFluorescent DyesFura-2Indicators and ReagentsMembrane ProteinsPhosphatidylinositol 4,5-DiphosphateTransient Receptor Potential Channelstrpl protein, DrosophilaType C Phospholipases

Identifiers

PMID11136854
PMCPMC2278390
OpenAlexW2038079237

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.