Evidence map›Paper›PMID 18621826›Full record

ArticleBiophysical journal2008

Intracellular calcium release channels mediate their own countercurrent: the ryanodine receptor case study.

Dirk Gillespie, Michael Fill

Abstract read
In one paragraph

Article in Biophysical journal, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed
–field-weighted citation impact
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

68 citing papers in PubMed.

  1. Review
  2. The diabetes-associated KDiabetologia · 2026
    Article
  3. Article
  4. Article
  5. Review
  6. CaJournal of molecular and cellular cardiology · 2023
    Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. How does flecainide impact RyR2 channel function?The Journal of general physiology · 2022
    Article
  13. Review
  14. TRIC-A regulates intracellular CaPflugers Archiv : European journal of physiology · 2021
    Review
  15. Simulating cardiac CaPflugers Archiv : European journal of physiology · 2021
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

8 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

2 authors.

Dirk GillespieDepartment of Molecular Biophysics and Physiology, Rush University Medical Center, Chicago, Illinois, USA. dirk_gillespie@rush.edu
Michael Fill

Funding

Skeletal Muscle Ryanodine Receptor Permeation and Self Counter-Ion FlowR01AR054098 · NIAMS · RUSH UNIVERSITY MEDICAL CENTER · PI FILL, MICHAEL · 2007 to 2017
$2.9M
Control of IP3R-Mediated Calcium ReleaseR01GM111397 · NIGMS · RUSH UNIVERSITY MEDICAL CENTER · PI CHEN, SUI RONG WAYNE, FILL, MICHAEL · 2015 to 2018
$1.6M
NIAMS NIH HHS AR054098NIAMS NIH HHS R01 AR054098
6 · The paper itself

Abstract

Intracellular calcium release channels like ryanodine receptors (RyRs) and inositol trisphosphate receptors (IP(3)Rs) mediate large Ca(2+) release events from Ca(2+) storage organelles lasting >5 ms. To have such long-lasting Ca(2+) efflux, a countercurrent of other ions is necessary to prevent the membrane potential from becoming the Ca(2+) Nernst potential in <1 ms. A recent model of ion permeation through a single, open RyR channel is used here to show that the vast majority of this countercurrent is conducted by the RyR itself. Consequently, changes in membrane potential are minimized locally and instantly, assuring maintenance of a Ca(2+)-driving force. This RyR autocountercurrent is possible because of the poor Ca(2+) selectivity and high conductance for both monovalent and divalent cations of these channels. The model shows that, under physiological conditions, the autocountercurrent clamps the membrane potential near 0 mV within approximately 150 mus. Consistent with experiments, the model shows how RyR unit Ca(2+) current is defined by luminal [Ca(2+)], permeable ion composition and concentration, and pore selectivity and conductance. This very likely is true of the highly homologous pore of the IP(3)R channel.

Indexed as

Ion Channel GatingCations, MonovalentIntracellular MembranesIntracellular SpaceMembrane PotentialsModels, BiologicalPermeabilityPotassiumRyanodine Receptor Calcium Release ChannelSarcoplasmic ReticulumCations, MonovalentPotassiumRyanodine Receptor Calcium Release Channel

Identifiers

PMID18621826
PMCPMC2553138

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.