Evidence map›Paper›PMID 22509043›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2012

Different agonists recruit different stromal interaction molecule proteins to support cytoplasmic Ca2+ oscillations and gene expression.

Pulak Kar, Daniel Bakowski, Joseph Di Capite, Charmaine Nelson, Anant B Parekh

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
8.2field-weighted citation impact, top 1% 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

54 citing papers in PubMed, 106 citations in OpenAlex.

  1. Activation of nuclear CaCell reports · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. CaJournal of cellular physiology · 2021
    Article
  6. The N terminus of Orai1 couples to the AKAP79 signaling complex to drive NFAT1 activation by local CaProceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  7. Review
  8. STIM2 targets Orai1/STIM1 to the AKAP79 signaling complex and confers coupling of CaProceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  9. Signaling through CaCold Spring Harbor perspectives in biology · 2020
    Review
  10. The whole-cell CaThe Journal of physiology · 2020
    Article
  11. Article
  12. Review
  13. Review
  14. Roles of CRAC channel in cancer: implications for therapeutic development.Expert review of precision medicine and drug development · 2020
    Article
  15. Store-Operated CaCancers · 2019
    Review
  16. STIM1 activation of Orai1.Cell calcium · 2019
    Review
  17. Article
  18. Review
  19. Interplay between ER CaInternational journal of molecular sciences · 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

5 authors at 1 institution in 2 countries.

Pulak KarDepartment of Physiology, Anatomy and Genetics, University of Oxford, Oxford OX1 3PT, United Kingdom.
Daniel Bakowski
Joseph Di Capite
Charmaine Nelson
Anant B Parekh
University of Oxford · GB

Funding

Medical Research Council G1000813
6 · The paper itself

Abstract

Stimulation of cells with physiological concentrations of calcium-mobilizing agonists often results in the generation of repetitive cytoplasmic Ca(2+) oscillations. Although oscillations arise from regenerative Ca(2+) release, they are sustained by store-operated Ca(2+) entry through Ca(2+) release-activated Ca(2+) (CRAC) channels. Here, we show that following stimulation of cysteinyl leukotriene type I receptors in rat basophilic leukemia (RBL)-1 cells, large amplitude Ca(2+) oscillations, CRAC channel activity, and downstream Ca(2+)-dependent nuclear factor of activated T cells (NFAT)-driven gene expression are all exclusively maintained by the endoplasmic reticulum Ca(2+) sensor stromal interaction molecule (STIM) 1. However, stimulation of tyrosine kinase-coupled FCεRI receptors evoked Ca(2+) oscillations and NFAT-dependent gene expression through recruitment of both STIM2 and STIM1. We conclude that different agonists activate different STIM proteins to sustain Ca(2+) signals and downstream responses.

Indexed as

AnimalsCalcium-Binding ProteinsCalcium ChannelsCalcium SignalingCell Line, TumorGene ExpressionGene Knockdown TechniquesLeukotriene C4Membrane GlycoproteinsMembrane ProteinsNFATC Transcription FactorsRatsReceptors, LeukotrieneStromal Interaction Molecule 1Stromal Interaction Molecule 2Calcium-Binding ProteinsCalcium ChannelsLeukotriene C4leukotriene D4 receptorMembrane GlycoproteinsMembrane ProteinsNFATC Transcription FactorsReceptors, LeukotrieneStim1 protein, ratSTIM2 protein, ratStromal Interaction Molecule 1Stromal Interaction Molecule 2

Identifiers

PMID22509043
PMCPMC3344999
OpenAlexW2066906512

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.