Evidence map›Paper›PMID 22201777›Full record

ReviewFrontiers in bioscience (Landmark edition)2012

STIM and Orai proteins and the non-capacitative ARC channels.

Trevor J Shuttleworth

Open access · bronzeAbstract readReview
In one paragraph

Review in Frontiers in bioscience (Landmark edition), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.6field-weighted citation impact, top 12% 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

14 citing papers in PubMed, 35 citations in OpenAlex.

  1. Neuronal Store-Operated Calcium Channels.Molecular neurobiology · 2023
    Review
  2. Review
  3. Article
  4. Article
  5. Orai channel-mediated Ca2+ signals in vascular and airway smooth muscle.American journal of physiology. Cell physiology · 2016
    Review
  6. Review
  7. Arachidonate-regulated Ca(2+) influx in human airway smooth muscle.American journal of respiratory cell and molecular biology · 2014
    Article
  8. Members of the thrombospondin gene family bind stromal interaction molecule 1 and regulate calcium channel activity.Matrix biology : journal of the International Society for Matrix Biology · 2014
    Article
  9. Article
  10. STIM1/Orai1-mediated SOCE: current perspectives and potential roles in cardiac function and pathology.American journal of physiology. Heart and circulatory physiology · 2013
    Review
  11. Article
  12. Article
  13. Review
  14. 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

1 author at 1 institution in 1 country.

Trevor J ShuttleworthDepartment of Pharmacology and Physiology, University of Rochester Medical Center, Rochester, NY 14642, USA. trevor_shuttleworth@urmc.rochester.edu
University of Rochester Medical Center · US

Funding

An experimental/computational approach for understanding salivary fluid secretionR01DE019245 · NIDCR · UNIVERSITY OF ROCHESTER · PI David I Yule · 2008 to 2026
$9.7M
RECEPTOR-REGULATED CALCIUM ENTRY IN EXOCRINE SECRETIONR01GM040457 · NIGMS · UNIVERSITY OF ROCHESTER · PI SHUTTLEWORTH, TREVOR J. · 1988 to 2017
$5.6M
Signaling Pathways in Salivary Gland Fluid SecretionR01DE016999 · NIDCR · UNIVERSITY OF ROCHESTER · PI SHUTTLEWORTH, TREVOR J. · 2005 to 2009
$1.8M
NIDCR NIH HHS R01 DE016999NIDCR NIH HHS R01 DE019245NIGMS NIH HHS R01 GM040457
6 · The paper itself

Abstract

The ARC channel is a small conductance, highly Ca²⁺-selective ion channel whose activation is specifically dependent on low concentrations of arachidonic acid acting at an intracellular site. They are widely distributed in diverse cell types where they provide an alternative, store-independent pathway for agonist-activated Ca²⁺ entry. Although biophysically similar to the store-operated CRAC channels, these two conductances function under distinct conditions of agonist stimulation, with the ARC channels providing the predominant route of Ca²⁺ entry during the oscillatory signals generated at low agonist concentrations. Despite these differences in function, like the CRAC channel, activation of the ARC channels is dependent on STIM1, but it is the pool of STIM1 that constitutively resides in the plasma membrane that is responsible. Similarly, both channels are formed by Orai proteins but, whilst the CRAC channel pore is a tetrameric assembly of Orai1 subunits, the ARC channel pore is formed by a heteropentameric assembly of three Orai1 subunits and two Orai3 subunits. There is increasing evidence that the activity of these channels plays a critical role in a variety of different cellular activities.

Indexed as

AnimalsCalcium ChannelsHumansMembrane ProteinsModels, MolecularNeoplasm ProteinsORAI1 ProteinProtein MultimerizationStromal Interaction Molecule 1Calcium ChannelsMembrane ProteinsNeoplasm ProteinsORAI1 ProteinORAI1 protein, humanSTIM1 protein, humanStromal Interaction Molecule 1

Identifiers

PMID22201777
PMCPMC3295580
OpenAlexW1548458029

What OpenQuestion holds

Textmetadata
LicenceTDM
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.