Evidence map›Paper›PMID 11695987›Full record

ArticleThe Biochemical journal2001

Regulation of Ca2+-release-activated Ca2+ current (Icrac) by ryanodine receptors in inositol 1,4,5-trisphosphate-receptor-deficient DT40 cells.

K Kiselyov, D M Shin, N Shcheynikov, T Kurosaki, S Muallem

Open access · bronzeAbstract read
In one paragraph

Article in The Biochemical journal, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
4.4field-weighted citation impact, top 5% 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

23 citing papers in PubMed, 60 citations in OpenAlex.

  1. Roles of NADMolecules (Basel, Switzerland) · 2020
    Review
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Expression of Orai genes and I(CRAC) activation in the human retinal pigment epithelium.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2011
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. On the activation mechanism of store-operated calcium channels.Pflugers Archiv : European journal of physiology · 2006
    Review
  14. Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. CCN3 and calcium signaling.Cell communication and signaling : CCS · 2003
    Article
  20. Ca2+ signalling and membrane current activated by cADPr in starfish oocytes.Pflugers Archiv : European journal of physiology · 2003
    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

5 authors at 2 institutions in 2 countries.

K KiselyovDepartment of Physiology, University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, TX 75390-9040, USA. kirill.kiselyov@UTSouthwestern.edu
D M Shin
N Shcheynikov
T Kurosaki
S Muallem
Kansai Medical University · JPThe University of Texas Southwestern Medical Center · US

Funding

MOLECULAR MECHANISMS OF ION TRANSPORT BY THE SMGR01DE012309 · NIDCR · UT SOUTHWESTERN MEDICAL CENTER · PI THOMAS, PHILIP J · 1997 to 2011
$4.4M
HORMONE REGULATION OF CA++ I- IN PANCREATIC ACINAR CELLSR01DK038938 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI STULL, JAMES TRAVIS · 1987 to 2010
$3.7M
NIDCR NIH HHS DE12309NIDDK NIH HHS DK38938
6 · The paper itself

Abstract

Persistence of capacitative Ca(2+) influx in inositol 1,4,5-trisphosphate (IP(3)) receptor (IP(3)R)-deficient DT40 cells (DT40(IP(3)R-/-)) raises the question of whether gating of Ca(2+)-release activated Ca(2+) current (I(crac)) by conformational coupling to Ca(2+)-release channels is a general mechanism of gating of these channels. In the present work we examined the properties and mechanism of activation of I(crac) Ca(2+) current in wild-type and DT40(IP(3)R-/-) cells. In both cell types passive depletion of internal Ca(2+) stores by infusion of EGTA activated a Ca(2+) current with similar characteristics and time course. The current was highly Ca(2+)-selective and showed strong inward rectification, all typical of I(crac). The activator of ryanodine receptor (RyR), cADP-ribose (cADPR), facilitated activation of I(crac), and the inhibitors of the RyRs, 8-N-cADPR, ryanodine and Ruthenium Red, all inhibited I(crac) activation in DT40(IP(3)R-/-) cells, even after complete depletion of intracellular Ca(2+) stores by ionomycin. Wild-type and DT40(IP(3)R-/-) cells express RyR isoforms 1 and 3. RyR levels were adapted in DT40(IP(3)R-/-) cells to a lower RyR3/RyR1 ratio than in wild-type cells. These results suggest that IP(3)Rs and RyRs can efficiently gate I(crac) in DT40 cells and explain the persistence of I(crac) gating by internal stores in the absence of IP(3)Rs.

Indexed as

Blotting, WesternCalciumCalcium ChannelsCell LineCells, CulturedDose-Response Relationship, DrugEgtazic AcidElectrophysiologyInositol 1,4,5-Trisphosphate ReceptorsPrecipitin TestsProtein ConformationProtein IsoformsReceptors, Cytoplasmic and NuclearReverse Transcriptase Polymerase Chain ReactionRyanodine Receptor Calcium Release ChannelCalciumCalcium ChannelsEgtazic AcidInositol 1,4,5-Trisphosphate ReceptorsProtein IsoformsReceptors, Cytoplasmic and NuclearRyanodine Receptor Calcium Release Channel

Identifiers

PMID11695987
PMCPMC1222197
OpenAlexW2032820299

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.