Evidence map›Paper›PMID 31553645›Full record

ArticleAmerican journal of physiology. Cell physiology2019

Novel interaction of antioxidant-1 with TRAF4: role in inflammatory responses in endothelial cells.

Archita Das, Varadarajan Sudhahar, Masuko Ushio-Fukai, Tohru Fukai

Open access · bronzeAbstract read
In one paragraph

Article in American journal of physiology. Cell physiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
0.7field-weighted citation impact, top 30% 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

22 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
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  3. The AGO2-ATOX1 axis exacerbates inflammation in a mouse sepsis model.Central-European journal of immunology · 2026
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  15. Copper chaperone antioxidant 1: multiple roles and a potential therapeutic target.Journal of molecular medicine (Berlin, Germany) · 2023
    Review
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  18. Article
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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 at 2 institutions in 1 country.

Archita DasVascular Biology Center, Medical College of Georgia at Augusta University, Augusta, Georgia.
Varadarajan SudhaharVascular Biology Center, Medical College of Georgia at Augusta University, Augusta, Georgia.
Masuko Ushio-FukaiVascular Biology Center, Medical College of Georgia at Augusta University, Augusta, Georgia.
Tohru FukaiVascular Biology Center, Medical College of Georgia at Augusta University, Augusta, Georgia.
Augusta University · USCharlie Norwood VA Medical Center · US

Funding

Vascular Extracellular Superoxide Dismutase ModulationR01HL070187 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI FUKAI, TOHRU · 2002 to 2017
$4.2M
Redox Regulation of Cu Importer CTR1 in AngiogenesisR01HL147550 · NHLBI · AUGUSTA UNIVERSITY · PI FUKAI, TOHRU, USHIO-FUKAI, MASUKO · 2020 to 2023
$3.3M
Copper transport protein and inflammatory angiogenesisR01HL116976 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI FUKAI, TOHRU, USHIO-FUKAI, MASUKO · 2013 to 2016
$2.9M
Cu Transporting ATPase and Diabetic Vascular ComplicationsR01HL133613 · NHLBI · AUGUSTA UNIVERSITY · PI FUKAI, TOHRU, USHIO-FUKAI, MASUKO · 2017 to 2020
$2.7M
Protein Disulfide Isomerase as Novel Redox Sensor in VEGF SignalingR01HL135584 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI USHIO-FUKAI, MASUKO · 2017 to 2020
$1.5M
SUMOylation of Cu transport protein Atox1 in AtherosclerosisI01BX001232 · VA · JESSE BROWN VA MEDICAL CENTER · PI TOHRU FUKAI · 2012 to 2026
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BLRD VA I01 BX001232NHLBI NIH HHS R01 HL070187NHLBI NIH HHS R01 HL116976NHLBI NIH HHS R01 HL133613NHLBI NIH HHS R01 HL135584NHLBI NIH HHS R01 HL147550
6 · The paper itself

Abstract

NADPH oxidase (NOX)-derived reactive oxygen species (ROS) and copper (Cu), an essential micronutrient, have been implicated in vascular inflammatory diseases. We reported that in proinflammatory cytokine TNF-α-stimulated endothelial cells (ECs), cytosolic Cu chaperone antioxidant-1 (Atox1) functions as a Cu-dependent transcription factor for the NOX organizer p47phox, thereby increasing ROS-dependent inflammatory gene expression. However, the role and mechanism of Atox1 nuclear translocation in inflamed ECs remain unclear. Using enface staining and nuclear fractionation, here we show that Atox1 was localized in the nucleus in inflamed aortas from ApoE

Indexed as

Angiotensin IIAnimalsAortaApolipoproteins EAtherosclerosisCopperCopper Transport ProteinsDiet, High-FatGene Expression RegulationHEK293 CellsHumansHuman Umbilical Vein Endothelial CellsInflammationIntercellular Adhesion Molecule-1MaleMiceAngiotensin IIApolipoproteins EAtox1 protein, mouseCopperCopper Transport ProteinsIcam1 protein, mouseIntercellular Adhesion Molecule-1Molecular ChaperonesNADPH Oxidasesneutrophil cytosolic factor 1Reactive Oxygen SpeciesRNA, Small InterferingTNF Receptor-Associated Factor 4Traf4 protein, mouseTumor Necrosis Factor-alphaVascular Cell Adhesion Molecule-1atherosclerosiscopper transport proteinendothelial cellsreactive oxygen speciesvascular inflammation

Identifiers

PMID31553645
PMCPMC6957386
OpenAlexW2976499838

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.