Evidence map›Paper›PMID 11423400›Full record

ArticleBiophysical journal2001

Single-channel recordings of recombinant inositol trisphosphate receptors in mammalian nuclear envelope.

D Boehning, S K Joseph, D O Mak, J K Foskett

Abstract read
In one paragraph

Article in Biophysical journal, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing 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

30 citing papers in PubMed.

  1. Review
  2. 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
  3. Review
  4. Review
  5. Review
  6. The acidocalcisome inositol-1,4,5-trisphosphate receptor ofThe Journal of biological chemistry · 2019
    Article
  7. All three IPScience signaling · 2018
    Article
  8. Article
  9. Cardiac inositol 1,4,5-trisphosphate receptors.Biochimica et biophysica acta. Molecular cell research · 2017
    Review
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. IP(3) receptors: toward understanding their activation.Cold Spring Harbor perspectives in biology · 2010
    Review
  17. Article
  18. Article
  19. Article
  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

4 authors.

D BoehningDepartment of Pathology and Cell Biology, Thomas Jefferson University, Philadelphia, Pennsylvania 19103, USA.
S K Joseph
D O Mak
J K Foskett

Funding

Alcohol Tissue InjuryT32AA007463 · NIAAA · THOMAS JEFFERSON UNIVERSITY · PI HOEK, JOANNES B, VADIGEPALLI, RAJANIKANTH · 1985 to 2021
$9.1M
MOLECULAR PHYSIOLOGY OF MAMMALIAN INSP3 RECEPTORSR01MH059937 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI FOSKETT, JAMES KEVIN · 2000 to 2014
$5.0M
MECHANISM OF INOSITOL TRISPHOSPHATE ACTIONR01DK034804 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI JOSEPH, SURESH K · 1986 to 2010
$2.7M
NIAAA NIH HHS T32-AA07463NIDDK NIH HHS R01-DK34804NIMH NIH HHS R01 MH059937NIMH NIH HHS R01-MH59937
6 · The paper itself

Abstract

Inositol 1,4,5-trisphosphate (InsP(3)) receptors (InsP(3)Rs) are intracellular Ca(2+) channels gated by the second messenger InsP(3). Here we describe a novel approach for recording single-channel currents through recombinant InsP(3)Rs in mammalian cells that applies patch-clamp electrophysiology to nuclei isolated from COS-7 cells transiently transfected with the neuronal (SII(+)) and peripheral (SII(-)) alternatively-spliced variants of the rat type 1 InsP(3)R. Single channels that were activated by InsP(3) and inhibited by heparin were observed in 45% of patches from nuclei prepared from transfected cells overexpressing recombinant InsP(3)Rs. In contrast, nuclei from cells transfected with the vector alone had InsP(3)-dependent channel activity in only 1.5% of patches. With K(+) (140 mM) as the permeant ion, recombinant SII(+) and SII(-) channels had slope conductances of 370 pS and 390 pS, respectively. The recombinant channels were 4-fold more selective for Ca(2+) over K(+), and their open probabilities were biphasically regulated by cytoplasmic [Ca(2+)]. This approach provides a powerful new methodology to study the permeation and gating properties of recombinant mammalian InsP(3)Rs in a native mammalian membrane environment at the single-channel level.

Indexed as

Alternative SplicingAnimalsCalciumCalcium ChannelsCell LineCOS CellsElectrophysiologyInositol 1,4,5-Trisphosphate ReceptorsIon Channel GatingNuclear EnvelopePatch-Clamp TechniquesProbabilityRatsReceptors, Cytoplasmic and NuclearRecombinant ProteinsCalciumCalcium ChannelsInositol 1,4,5-Trisphosphate ReceptorsReceptors, Cytoplasmic and NuclearRecombinant Proteins

Identifiers

PMID11423400
PMCPMC1301497

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.