Evidence map›Paper›PMID 23690558›Full record

ArticleThe Journal of physiology2013

Molecular basis of activation of the arachidonate-regulated Ca2+ (ARC) channel, a store-independent Orai channel, by plasma membrane STIM1.

Jill L Thompson, Trevor J Shuttleworth

Open access · greenAbstract read
In one paragraph

Article in The Journal of physiology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

27 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
  2. A Model for the Coexistence of Competing Mechanisms forBulletin of mathematical biology · 2024
    Article
  3. Article
  4. p38 MAPK activation and STIM1-Orai3 association mediate TRPC6 externalization.American journal of physiology. Cell physiology · 2023
    Article
  5. Review
  6. Article
  7. Article
  8. Role of Store-Operated CaBiomolecules · 2021
    Review
  9. Review
  10. Review
  11. The anatomy ofCurrent opinion in physiology · 2020
    Article
  12. Article
  13. Article
  14. The role of CaCell calcium · 2018
    Review
  15. Review
  16. Article
  17. Article
  18. Store-Operated Calcium Entry in Müller Glia Is Controlled by Synergistic Activation of TRPC and Orai Channels.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2016
    Article
  19. Store-Operated Calcium Channels.Physiological reviews · 2015
    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

2 authors at 1 institution in 1 country.

Jill L ThompsonDepartment of Pharmacology and Physiology, University of Rochester Medical Center, Rochester, NY 14642, USA.
Trevor J Shuttleworth
University of Rochester Medical Center · US

Funding

RECEPTOR-REGULATED CALCIUM ENTRY IN EXOCRINE SECRETIONR01GM040457 · NIGMS · UNIVERSITY OF ROCHESTER · PI SHUTTLEWORTH, TREVOR J. · 1988 to 2017
$5.6M
NIGMS NIH HHS GM040457NIGMS NIH HHS R01 GM040457
6 · The paper itself

Abstract

Currently, Orai proteins are known to encode two distinct agonist-activated, highly calcium-selective channels: the store-operated Ca(2+) release-activated Ca(2+) (CRAC) channels, and the store-independent, arachidonic acid-activated ARC channels. Surprisingly, whilst the trigger for activation of these channels is entirely different, both depend on stromal interacting molecule 1 (STIM1). However, whilst STIM1 in the endoplasmic reticulum membrane is the critical sensor for the depletion of this calcium store that triggers CRAC channel activation, it is the pool of STIM1 constitutively resident in the plasma membrane that is essential for activation of the ARC channels. Here, using a variety of approaches, we show that the key domains within the cytosolic part of STIM1 identified as critical for the activation of CRAC channels are also key for activation of the ARC channels. However, examination of the actual steps involved in such activation reveal marked differences between these two Orai channel types. Specifically, loss of calcium from the EF-hand of STIM1 that forms the key initiation point for activation of the CRAC channels has no effect on ARC channel activity. Secondly, in marked contrast to the dynamic and labile nature of interactions between STIM1 and the CRAC channels, STIM1 in the plasma membrane appears to be constitutively associated with the ARC channels. Finally, specific mutations in STIM1 that induce an extended, constitutively active, conformation for the CRAC channels actually prevent activation of the ARC channels by arachidonic acid. Based on these findings, we propose that the likely role of arachidonic acid lies in inducing the actual gating of the channel.

Indexed as

Arachidonic AcidCalcium ChannelsCell MembraneHEK293 CellsHumansMembrane ProteinsNeoplasm ProteinsStromal Interaction Molecule 1Arachidonic AcidCalcium ChannelsMembrane ProteinsNeoplasm ProteinsSTIM1 protein, humanStromal Interaction Molecule 1

Identifiers

PMID23690558
PMCPMC3731610
OpenAlexW1518148880

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.