Evidence map›Paper›PMID 19934435›Full record

ArticleScience signaling2009

Ca(2+) puffs originate from preestablished stable clusters of inositol trisphosphate receptors.

Ian F Smith, Steven M Wiltgen, Jianwei Shuai, Ian Parker

Open access · greenAbstract read
In one paragraph

Article in Science signaling, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

48 citing papers in PubMed, 83 citations in OpenAlex.

  1. Phosphorylation of Bok at Ser-8 blocks its ability to suppress IPCell communication and signaling : CCS · 2025
    Article
  2. Review
  3. Article
  4. Understanding IPCell calcium · 2023
    Review
  5. Dissociation of inositol 1,4,5-trisphosphate from IPThe Journal of biological chemistry · 2023
    Article
  6. Functional determination of calcium-binding sites required for the activation of inositol 1,4,5-trisphosphate receptors.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  7. Termination of CaCell calcium · 2021
    Article
  8. KRAP tethers IPNature communications · 2021
    Article
  9. Article
  10. Article
  11. Spatial-temporal patterning of CaSeminars in cell & developmental biology · 2019
    Review
  12. Article
  13. Article
  14. Structure and Function of IPCold Spring Harbor perspectives in biology · 2019
    Review
  15. All three IPScience signaling · 2018
    Article
  16. Article
  17. All three IPJournal of cell science · 2018
    Article
  18. Dynamic CaCell calcium · 2018
    Article
  19. Article
  20. CaNature communications · 2017
    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 2 institutions in 2 countries.

Ian F SmithDepartment of Neurobiology and Behavior, University of California, Irvine, CA 92697-4550, USA. ismith@uci.edu
Steven M Wiltgen
Jianwei Shuai
Ian Parker
University of California, Irvine · USXiamen University · CN

Funding

Multi-scale observation and modeling of IP3/Ca signalingR01GM065830 · NIGMS · UNIVERSITY OF CALIF-LOS ALAMOS NAT LAB · PI MAK, DON-ON DANIEL, PARKER, IAN · 2002 to 2017
$10.7M
Elementary Events of Intracellular Calcium SignalingR37GM048071 · NIGMS · UNIVERSITY OF CALIFORNIA-IRVINE · PI PARKER, IAN · 2011 to 2020
$5.3M
SPATIAL AND TEMPORAL ASPECTS OF INSP3 SIGNALLINGR01GM048071 · NIGMS · UNIVERSITY OF CALIFORNIA-IRVINE · PI PARKER, IAN · 1992 to 2010
$3.9M
NIGMS NIH HHS R01 GM048071NIGMS NIH HHS R01 GM065830NIGMS NIH HHS R37 GM048071
6 · The paper itself

Abstract

Intracellular calcium ion (Ca(2+)) signaling crucially depends on the clustered organization of inositol trisphosphate receptors (IP(3)Rs) in the endoplasmic reticulum (ER) membrane. These ligand-gated ion channels liberate Ca(2+) to generate local signals known as Ca(2+) puffs. We tested the hypothesis that IP(3) itself elicits rapid clustering of IP(3)Rs by using flash photolysis of caged IP(3) in conjunction with high-resolution Ca(2+) imaging to monitor the activity and localization of individual IP(3)Rs within intact mammalian cells. Our results indicate that Ca(2+) puffs arising with latencies as short as 100 to 200 ms after photorelease of IP(3) already involve at least four IP(3)R channels, and that this number does not subsequently grow. Moreover, single active IP(3)Rs show limited mobility, and stochastic simulations suggest that aggregation of IP(3)Rs at puff sites by a diffusional trapping mechanism would require many seconds. We thus conclude that puff sites represent preestablished, stable clusters of IP(3)Rs and that functional IP(3)Rs are not readily diffusible within the ER membrane.

Indexed as

CalciumCalcium SignalingCell Line, TumorCluster AnalysisComputer SimulationEndoplasmic ReticulumHeLa CellsHumansInositol 1,4,5-Trisphosphate ReceptorsIonsLigandsMicroscopy, FluorescenceModels, BiologicalSignal TransductionStochastic ProcessesCalciumInositol 1,4,5-Trisphosphate ReceptorsIonsLigands

Identifiers

PMID19934435
PMCPMC2897231
OpenAlexW2042892520

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.