Evidence map›Paper›PMID 17905723›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2008

STIM2 protein mediates distinct store-dependent and store-independent modes of CRAC channel activation.

Suhel Parvez, Andreas Beck, Christine Peinelt, Jonathan Soboloff, Annette Lis, Mahealani Monteilh-Zoller, Donald L Gill, Andrea Fleig, Reinhold Penner

Open access · greenAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 90 papers.

0numbers the graph read from it
0cells of the map it votes in
90citing papers in PubMed
6.0field-weighted citation impact, top 3% 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

90 citing papers in PubMed, 152 citations in OpenAlex.

  1. Article
  2. Essential role of N-terminal SAM regions in STIM1 multimerization and function.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  3. Article
  4. Role of store-operated Ca2+ entry in cardiovascular disease.Cell communication and signaling : CCS · 2022
    Review
  5. Review
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. The Number and Position of Orai3 Units within Heteromeric Store-Operated CaInternational journal of molecular sciences · 2020
    Article
  13. Review
  14. Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Interplay between ER CaInternational journal of molecular sciences · 2018
    Article

30 more citing papers are in PubMed but not listed here.

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

9 authors at 4 institutions in 1 country.

Suhel ParvezCenter for Biomedical Research and John A. Burns School of Medicine, University of Hawaii, Honolulu, Hawaii 96813, USA.
Andreas Beck
Christine Peinelt
Jonathan Soboloff
Annette Lis
Mahealani Monteilh-Zoller
Donald L Gill
Andrea Fleig
Reinhold Penner
Queen's Medical Center · USTemple University · USUniversity of Hawaiʻi at Mānoa · USUniversity of Hawaii System · US

Funding

Control of Calcium Entry Signals in B CellsR01AI058173 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI GILL, DONALD L · 2004 to 2014
$3.7M
Inositol (1,4,5) trisphoshate response thresholdsR01AI050200 · NIAID · QUEEN'S MEDICAL CENTER · PI PENNER, REINHOLD · 2004 to 2008
$1.9M
CALCIUM SIGNALING ACTIVATION PROCESS OF MICROGLIA CELLSR01NS040927 · NINDS · QUEEN'S MEDICAL CENTER · PI PENNER, REINHOLD · 2001 to 2005
$1.8M
NIAID NIH HHS AI058173NIAID NIH HHS R01 AI050200NIAID NIH HHS R01-AI050200NIAID NIH HHS R01 AI058173NINDS NIH HHS R01 NS040927NINDS NIH HHS R01-NS040927
6 · The paper itself

Abstract

STIM1 and CRACM1 (or Orai1) are essential molecular components mediating store-operated Ca2+ entry (SOCE) and Ca2+ release-activated Ca2+ (CRAC) currents. Although STIM1 acts as a luminal Ca2+ sensor in the endoplasmic reticulum (ER), the function of STIM2 remains unclear. Here we reveal that STIM2 has two distinct modes of activating CRAC channels: a store-operated mode that is activated through depletion of ER Ca2+ stores by inositol 1,4,5-trisphosphate (InsP3) and store-independent activation that is mediated by cell dialysis during whole-cell perfusion. Both modes are regulated by calmodulin (CaM). The store-operated mode is transient in intact cells, possibly reflecting recruitment of CaM, whereas loss of CaM in perfused cells accounts for the persistence of the store-independent mode. The inhibition by CaM can be reversed by 2-aminoethoxydiphenyl borate (2-APB), resulting in rapid, store-independent activation of CRAC channels. The aminoglycoside antibiotic G418 is a highly specific and potent inhibitor of STIM2-dependent CRAC channel activation. The results reveal a novel bimodal control of CRAC channels by STIM2, the store dependence and CaM regulation, which indicates that the STIM2/CRACM1 complex may be under the control of both luminal and cytoplasmic Ca2+ levels.

Indexed as

CalciumCalcium ChannelsCalmodulinCell Adhesion MoleculesCell LineCytoplasmHumansMembrane ProteinsORAI1 ProteinStromal Interaction Molecule 2Up-RegulationCalciumCalcium ChannelsCalmodulinCell Adhesion MoleculesMembrane ProteinsORAI1 ProteinORAI1 protein, humanSTIM2 protein, humanStromal Interaction Molecule 2

Identifiers

PMID17905723
PMCPMC3601890
OpenAlexW2049960163

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.