Evidence map›Paper›PMID 37132383›Full record

ArticleCirculation research2023

A Critical Role for ERO1α in Arterial Thrombosis and Ischemic Stroke.

Vishwanath Jha, Bei Xiong, Tripti Kumari, Gavriel Brown, Jinzhi Wang, Kyungho Kim, Jingu Lee, Nathan Asquith, John Gallagher, Lillian Asherman and 10 more

Open access · bronzeAbstract read
In one paragraph

Article in Circulation research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
4.1field-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

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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

17 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
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  5. Classification of Protein Disulfide Bonds.Methods in molecular biology (Clifton, N.J.) · 2026
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  9. EROdicating arterial thrombosis with a novel endoplasmic reticulum oxidoreductase 1α inhibitor.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Article
  10. Review
  11. 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

20 authors at 9 institutions in 5 countries.

Vishwanath Jha *Division of Hematology, Department of Medicine (V.J., T.K., G.B., J.W., J.L., J.G., L.A., T.L., J.C.), Washington University School of Medicine, St. Louis, MO.ORCID 0000-0001-6085-8138
Bei Xiong *Department of Hematology, Zhongnan Hospital of Wuhan University, Hubei, People's Republic of China (B.X.).
Tripti KumariDivision of Hematology, Department of Medicine (V.J., T.K., G.B., J.W., J.L., J.G., L.A., T.L., J.C.), Washington University School of Medicine, St. Louis, MO.
Gavriel BrownDivision of Hematology, Department of Medicine (V.J., T.K., G.B., J.W., J.L., J.G., L.A., T.L., J.C.), Washington University School of Medicine, St. Louis, MO.
Jinzhi WangDivision of Hematology, Department of Medicine (V.J., T.K., G.B., J.W., J.L., J.G., L.A., T.L., J.C.), Washington University School of Medicine, St. Louis, MO.ORCID 0000-0001-5135-7139
Kyungho KimKorean Medicine-Application Center, Korea Institute of Oriental Medicine, Daegu (K.K.).
Jingu LeeDivision of Hematology, Department of Medicine (V.J., T.K., G.B., J.W., J.L., J.G., L.A., T.L., J.C.), Washington University School of Medicine, St. Louis, MO.
Nathan AsquithDepartment of Medicine, Harvard Medical School, Boston, MA (N.A., J.E.I.).ORCID 0000-0002-7073-825X
John GallagherDivision of Hematology, Department of Medicine (V.J., T.K., G.B., J.W., J.L., J.G., L.A., T.L., J.C.), Washington University School of Medicine, St. Louis, MO.
Lillian AshermanDivision of Hematology, Department of Medicine (V.J., T.K., G.B., J.W., J.L., J.G., L.A., T.L., J.C.), Washington University School of Medicine, St. Louis, MO.ORCID 0000-0003-1611-4910
Taylor LambertDivision of Hematology, Department of Medicine (V.J., T.K., G.B., J.W., J.L., J.G., L.A., T.L., J.C.), Washington University School of Medicine, St. Louis, MO.
Yanyan BaiDepartment of Pharmacology and Regenerative Medicine, University of Illinois College of Medicine at Chicago (Y.B., X.D.).ORCID 0000-0002-8365-8451
Xiaoping DuDepartment of Pharmacology and Regenerative Medicine, University of Illinois College of Medicine at Chicago (Y.B., X.D.).ORCID 0000-0001-9842-8192
Jeong-Ki MinBiotherapeutics Translational Research Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon (J.-K.M.).
Rajan SahCardiovascular Division, Department of Medicine (R.S., A.J.), Washington University School of Medicine, St. Louis, MO.
Ali JavaheriCardiovascular Division, Department of Medicine (R.S., A.J.), Washington University School of Medicine, St. Louis, MO.ORCID 0000-0001-6657-331X
Babak RazaniVascular Medicine Institute, Department of Medicine, University of Pittsburgh School of Medicine and UPMC, Pittsburgh, PA (B.R.).ORCID 0000-0002-7172-9240
Jin-Moo LeeDepartment of Neurology (J.-M.L.), Washington University School of Medicine, St. Louis, MO.ORCID 0000-0002-3979-0906
Joseph E ItalianoDepartment of Medicine, Harvard Medical School, Boston, MA (N.A., J.E.I.).ORCID 0000-0001-6547-9663
Jaehyung ChoDivision of Hematology, Department of Medicine (V.J., T.K., G.B., J.W., J.L., J.G., L.A., T.L., J.C.), Washington University School of Medicine, St. Louis, MO.ORCID 0000-0003-2404-3446
Washington University in St. Louis · USBoston Children's Hospital · USIllinois College · USJikei University School of Medicine · JPJohn Brown University · USKorea Institute of Oriental Medicine · KRKorea Research Institute of Bioscience and Biotechnology · KRUniversity of Pittsburgh · USWuhan University · CN

Funding

Washington University Center for Cellular ImagingP30CA091842 · NCI · WASHINGTON UNIVERSITY · PI AIMEE S JAMES · 2001 to 2026
$128.0M
WU INSTITUTE OF CLINICAL AND TRANSLATIONAL SCIENCESUL1TR002345 · NCATS · WASHINGTON UNIVERSITY · PI William G. Powderly · 2017 to 2026
$97.8M
Washington University Institute of Clinical and Translational SciencesUL1TR000448 · NCATS · WASHINGTON UNIVERSITY · PI EVANOFF, BRADLEY A · 2012 to 2016
$41.4M
TrainingP41GM103422 · NIGMS · WASHINGTON UNIVERSITY · PI YARASHESKI, KEVIN E · 2012 to 2019
$12.0M
Mechanisms of integrin signaling and a new anti-platelet/anti-inflammatory approachR35HL150797 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI Xiaoping Du · 2020 to 2026
$6.8M
The Centrosome as a master controller of platelet production.R35HL161175 · NHLBI · BOSTON CHILDREN'S HOSPITAL · PI JOSEPH E ITALIANO · 2022 to 2026
$5.3M
THE ROLE OF MACROPHAGE LYSOSOMAL BIOGENESIS IN ATHEROSCLEROSISR01HL125838 · NHLBI · WASHINGTON UNIVERSITY · PI RAZANI, BABAK · 2015 to 2025
$4.6M
Thiol isomerases in neutrophil recruitment and thromboinflammatory diseaseR01HL130028 · NHLBI · WASHINGTON UNIVERSITY · PI CHO, JAEHYUNG · 2016 to 2024
$3.6M
Dissecting the Impact of Dietary Protein on Macrophage mTOR Signaling and AtherosclerosisR01HL159461 · NHLBI · WASHINGTON UNIVERSITY · PI Bettina Mittendorfer, Babak Razani · 2022 to 2026
$3.3M
Harnessing macrophage lysosomal lipid metabolism in obesity-associated diseasesR01DK131188 · NIDDK · WASHINGTON UNIVERSITY · PI MITTENDORFER, BETTINA, RAZANI, BABAK · 2022 to 2025
$2.6M
A Biomedical Mass Spectrometry Resource: Ongoing Driving Biomedical ProjectsR24GM136766 · NIGMS · WASHINGTON UNIVERSITY · PI GROSS, MICHAEL L · 2020 to 2022
$2.3M
Thiol isomerases and ERO1α in sickle cell vaso-occlusionR01HL148280 · NHLBI · WASHINGTON UNIVERSITY · PI CHO, JAEHYUNG · 2019 to 2022
$1.9M
BLRD VA I01 BX003415NCATS NIH HHS UL1 TR000448NCATS NIH HHS UL1 TR002345NCI NIH HHS P30 CA091842NHLBI NIH HHS R01 HL125838NHLBI NIH HHS R01 HL130028NHLBI NIH HHS R01 HL146559NHLBI NIH HHS R01 HL148280NHLBI NIH HHS R01 HL153047NHLBI NIH HHS R01 HL159461NHLBI NIH HHS R35 HL150797NHLBI NIH HHS R35 HL161175NIDDK NIH HHS R01 DK131188NIGMS NIH HHS P41 GM103422NIGMS NIH HHS R24 GM136766
6 · The paper itself

Abstract

backgroundPlatelet adhesion and aggregation play a crucial role in arterial thrombosis and ischemic stroke. Here, we identify platelet ERO1α (endoplasmic reticulum oxidoreductase 1α) as a novel regulator of Ca

methodsIntravital microscopy, animal disease models, and a wide range of cell biological studies were utilized to demonstrate the pathophysiological role of ERO1α in arteriolar and arterial thrombosis and to prove the importance of platelet ERO1α in platelet activation and aggregation. Mass spectrometry, electron microscopy, and biochemical studies were used to investigate the molecular mechanism. We used novel blocking antibodies and small-molecule inhibitors to study whether ERO1α can be targeted to attenuate thrombotic conditions.

resultsMegakaryocyte-specific or global deletion of Ero1α in mice similarly reduced platelet thrombus formation in arteriolar and arterial thrombosis without affecting tail bleeding times and blood loss following vascular injury. We observed that platelet ERO1α localized exclusively in the dense tubular system and promoted Ca

conclusionsOur results suggest that ERO1α acts as a thiol oxidase for Ca

Indexed as

Ischemic StrokeThrombosisAnimalsBlood PlateletsCalcium SignalingDisulfidesMiceOxidoreductasesPlatelet ActivationDisulfidesEro1a protein, mouseOxidoreductasescalcium signalingischemic strokeplatelet activationthrombosis

Identifiers

PMID37132383
PMCPMC10213138
OpenAlexW4367834490

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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.