Evidence map›Paper›PMID 19348050›Full record

ArticleNature2009

Clustering of InsP3 receptors by InsP3 retunes their regulation by InsP3 and Ca2+.

Taufiq-Ur-Rahman, Alexander Skupin, Martin Falcke, Colin W Taylor

Open access · greenAbstract read
In one paragraph

Article in Nature, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 83 papers.

0numbers the graph read from it
0cells of the map it votes in
83citing papers in PubMed
11.2field-weighted citation impact, top 1% 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

83 citing papers in PubMed, 169 citations in OpenAlex.

  1. Article
  2. Conformational landscape and clustering of human type 2 IPbioRxiv : the preprint server for biology · 2026
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  3. Article
  4. Modeling traveling calcium waves in cellular structures.Journal of computational neuroscience · 2025
    Article
  5. Article
  6. Structural titration reveals CaNature communications · 2023
    Article
  7. Synergistic Interaction of 5-HTInternational journal of molecular sciences · 2023
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  8. Understanding IPCell calcium · 2023
    Review
  9. Modeling IPBiophysical journal · 2023
    Article
  10. Ratiometric measurement of MAM CaNature communications · 2023
    Article
  11. Characterizing spontaneous CaBiophysical journal · 2022
    Article
  12. Review
  13. Quantal CaCell reports · 2021
    Article
  14. IPProceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  15. Article
  16. Article
  17. Spatial-temporal patterning of CaSeminars in cell & developmental biology · 2019
    Review
  18. The acidocalcisome inositol-1,4,5-trisphosphate receptor ofThe Journal of biological chemistry · 2019
    Article
  19. Article
  20. Review

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 3 institutions in 2 countries.

Taufiq-Ur-RahmanDepartment of Pharmacology, Tennis Court Road, Cambridge CB2 1PD, UK.
Alexander Skupin
Martin Falcke
Colin W Taylor
Lawn Tennis Association · GBHelmholtz-Zentrum Berlin für Materialien und Energie · DEMax Delbrück Center · DE

Funding

Biotechnology and Biological Sciences Research Council BBE0046601Wellcome Trust 085295
6 · The paper itself

Abstract

The versatility of Ca2+ signals derives from their spatio-temporal organization. For Ca2+ signals initiated by inositol-1,4,5-trisphosphate (InsP3), this requires local interactions between InsP3 receptors (InsP3Rs) mediated by their rapid stimulation and slower inhibition\ by cytosolic Ca2+. This allows hierarchical recruitment of Ca2+ release events as the InsP3 concentration increases. Single InsP3Rs respond first, then clustered InsP3Rs open together giving a local 'Ca2+ puff', and as puffs become more frequent they ignite regenerative Ca2+ waves. Using nuclear patch-clamp recording, here we demonstrate that InsP3Rs are initially randomly distributed with an estimated separation of 1 m. Low concentrations of InsP3 cause InsP3Rs to aggregate rapidly and reversibly into small clusters of about four closely associated InsP3Rs. At resting cytosolic [Ca2+], clustered InsP3Rs open independently, but with lower open probability, shorter open time, and less InsP3 sensitivity than lone InsP3Rs. Increasing cytosolic [Ca2+] reverses the inhibition caused by clustering, InsP3R gating becomes coupled, and the duration of multiple openings is prolonged. Clustering both exposes InsP3Rs to local Ca2+ rises and increases the effects of Ca2+. Dynamic regulation of clustering by InsP3 retunes InsP3R sensitivity to InsP3 and Ca2+, facilitating hierarchical recruitment of the elementary events that underlie all InsP3-evoked Ca2+ signals.

Indexed as

Calcium SignalingAnimalsCalciumCell LineCytosolInositol 1,4,5-TrisphosphateInositol 1,4,5-Trisphosphate ReceptorsIon Channel GatingPatch-Clamp TechniquesProtein TransportRatsCalciumInositol 1,4,5-TrisphosphateInositol 1,4,5-Trisphosphate Receptors

Identifiers

PMID19348050
PMCPMC2702691
OpenAlexW2853874477

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.