Evidence map›Paper›PMID 24469450›Full record

ArticleThe Journal of biological chemistry2014

Isoform- and species-specific control of inositol 1,4,5-trisphosphate (IP3) receptors by reactive oxygen species.

Száva Bánsághi, Tünde Golenár, Muniswamy Madesh, György Csordás, Satish RamachandraRao, Kumar Sharma, David I Yule, Suresh K Joseph, György Hajnóczky

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 81 papers.

0numbers the graph read from it
0cells of the map it votes in
81citing papers in PubMed
8.2field-weighted citation impact, top 2% 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

81 citing papers in PubMed, 138 citations in OpenAlex.

  1. Article
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  8. IPAntioxidants (Basel, Switzerland) · 2024
    Article
  9. TFAM and Mitochondrial Protection in Diabetic Kidney Disease.Diabetes, metabolic syndrome and obesity : targets and therapy · 2024
    Review
  10. Review
  11. Review
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  14. Article
  15. Review
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  17. Antioxidants (Basel, Switzerland) · 2022
    Review
  18. Article
  19. Review
  20. Amyloid-Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2022
    Article

21 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

9 authors at 2 institutions in 1 country.

Száva BánsághiFrom the MitoCare Center, Department of Pathology, Anatomy and Cell Biology, Thomas Jefferson University, Philadelphia, Pennsylvania 19107.
Tünde Golenár
Muniswamy Madesh
György Csordás
Satish RamachandraRao
Kumar Sharma
David I Yule
Suresh K Joseph
György Hajnóczky
Thomas Jefferson University · USUniversity of Rochester Medical Center · US

Funding

Novel Paradigms in Diabetic ComplicationsDP3DK094352 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI SHARMA, KUMAR · 2011 to 2011
$6.0M
MITOCHONDRIAL CALCIUM SIGNALING IN CELL DEATHR01GM059419 · NIGMS · THOMAS JEFFERSON UNIVERSITY · PI HAJNOCZKY, GYORGY · 2000 to 2016
$4.0M
MECHANISM OF INOSITOL TRISPHOSPHATE ACTIONR01DK034804 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI JOSEPH, SURESH K · 1986 to 2010
$2.7M
TGF-b signaling in diabetic kidney diseaseR01DK053867 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI SHARMA, KUMAR · 1999 to 2009
$2.5M
NIDDK NIH HHS DK053867NIDDK NIH HHS DK34804NIDDK NIH HHS DP3 DK094352NIDDK NIH HHS R01 DK034804NIDDK NIH HHS R01 DK053867NIGMS NIH HHS GM059419NIGMS NIH HHS R01 GM059419
6 · The paper itself

Abstract

Reactive oxygen species (ROS) stimulate cytoplasmic [Ca(2+)] ([Ca(2+)]c) signaling, but the exact role of the IP3 receptors (IP3R) in this process remains unclear. IP3Rs serve as a potential target of ROS produced by both ER and mitochondrial enzymes, which might locally expose IP3Rs at the ER-mitochondrial associations. Also, IP3Rs contain multiple reactive thiols, common molecular targets of ROS. Therefore, we have examined the effect of superoxide anion (O2) on IP3R-mediated Ca(2+) signaling. In human HepG2, rat RBL-2H3, and chicken DT40 cells, we observed [Ca(2+)]c spikes and frequency-modulated oscillations evoked by a O2 donor, xanthine (X) + xanthine oxidase (XO), dose-dependently. The [Ca(2+)]c signal was mediated by ER Ca(2+) mobilization. X+XO added to permeabilized cells promoted the [Ca(2+)]c rise evoked by submaximal doses of IP3, indicating that O2 directly sensitizes IP3R-mediated Ca(2+) release. In response to X+XO, DT40 cells lacking two of three IP3R isoforms (DKO) expressing either type 1 (DKO1) or type 2 IP3Rs (DKO2) showed a [Ca(2+)]c signal, whereas DKO expressing type 3 IP3R (DKO3) did not. By contrast, IgM that stimulates IP3 formation, elicited a [Ca(2+)]c signal in every DKO. X+XO also facilitated the Ca(2+) release evoked by submaximal IP3 in permeabilized DKO1 and DKO2 but was ineffective in DKO3 or in DT40 lacking every IP3R (TKO). However, X+XO could also facilitate the effect of suboptimal IP3 in TKO transfected with rat IP3R3. Although in silico studies failed to identify a thiol missing in the chicken IP3R3, an X+XO-induced redox change was documented only in the rat IP3R3. Thus, ROS seem to specifically sensitize IP3Rs through a thiol group(s) within the IP3R, which is probably inaccessible in the chicken IP3R3.

Indexed as

Amino Acid SequenceAnimalsCalcium SignalingCell LineChickensHumansInositol 1,4,5-TrisphosphateInositol 1,4,5-Trisphosphate ReceptorsMitochondriaMolecular Sequence DataProtein IsoformsRatsReactive Oxygen SpeciesSequence AlignmentSpecies SpecificityInositol 1,4,5-TrisphosphateInositol 1,4,5-Trisphosphate ReceptorsProtein IsoformsReactive Oxygen SpeciesCalcium SignalingEndoplasmic Reticulum (ER)Inositol 1,4,5-TrisphosphateIP3 ReceptorMitochondriaReactive Oxygen Species (ROS)

Identifiers

PMID24469450
PMCPMC3961646
OpenAlexW2018995978

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.