Evidence map›Paper›PMID 30185837›Full record

ArticleScientific reports2018

Association of the IP3R to STIM1 provides a reduced intraluminal calcium microenvironment, resulting in enhanced store-operated calcium entry.

Alicia Sampieri, Karla Santoyo, Alexander Asanov, Luis Vaca

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

32 citing papers in PubMed, 56 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Plants (Basel, Switzerland) · 2023
    Article
  6. Article
  7. Review
  8. Review
  9. Roles of CaBiochemistry and biophysics reports · 2022
    Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Functional communication between IPProceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  16. Article
  17. Review
  18. Review
  19. Review
  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

4 authors at 1 institution in 1 country.

Alicia SampieriDepartamento de Biologia Celular y del Desarrollo, Instituto de Fisiología Celular. Universidad Nacional Autonoma de México, Ciudad de México, Mexico.
Karla SantoyoDepartamento de Biologia Celular y del Desarrollo, Instituto de Fisiología Celular. Universidad Nacional Autonoma de México, Ciudad de México, Mexico.
Alexander AsanovTIRFLabs Inc, 106 Grendon Place, Cary, NC, USA.
Luis VacaDepartamento de Biologia Celular y del Desarrollo, Instituto de Fisiología Celular. Universidad Nacional Autonoma de México, Ciudad de México, Mexico. lvaca@ifc.unam.mx.ORCID 0000-0003-2266-4847
Universidad Nacional Autónoma de México · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The involvement of inositol trisphosphate receptor (IP3R) in modulating store-operated calcium entry (SOCE) was established many years ago. Nevertheless, the molecular mechanism responsible for this observation has not been elucidated to this date. In the present study we show that IP3R associates to STIM1 upon depletion of the endoplasmic reticulum (ER) by activation of the inositol trisphosphate signaling cascade via G-protein coupled receptors. IP3R-STIM1 association results in enhanced STIM1 puncta formation and larger Orai-mediated whole-cell currents as well as increased calcium influx. Depleting the ER with a calcium ATPase inhibitor (thapsigargin, TG) does not induce IP3R-STIM1 association, indicating that this association requires an active IP3R. The IP3R-STIM1 association is only observed after IP3R activation, as evidenced by FRET experiments and co-immunoprecipitation assays. ER intraluminal calcium measurements using Mag-Fluo-4 showed enhanced calcium depletion when IP3R is overexpressed. A STIM1-GCaMP fusion protein indicates that STIM1 detects lower calcium concentrations near its EF-hand domain when IP3R is overexpressed when compared with the fluorescence reported by a GCaMP homogenously distributed in the ER lumen (ER-GCaMP). All these data together strongly suggest that activation of inositol trisphosphate signaling cascade induces the formation of the IP3R-STIM1 complex. The activated IP3R provides a reduced intraluminal calcium microenvironment near STIM1, resulting in enhanced activation of Orai currents and SOCE.

Indexed as

CalciumEF Hand MotifsEndoplasmic ReticulumHEK293 CellsHumansInositol 1,4,5-Trisphosphate ReceptorsInositol PhosphatesNeoplasm ProteinsReceptors, G-Protein-CoupledSignal TransductionStromal Interaction Molecule 1CalciumInositol 1,4,5-Trisphosphate ReceptorsInositol Phosphatesinositol trispyrophosphateNeoplasm ProteinsReceptors, G-Protein-CoupledSTIM1 protein, humanStromal Interaction Molecule 1

Identifiers

PMID30185837
PMCPMC6125598
OpenAlexW2889484312

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Registered trials

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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.