Evidence map›Paper›PMID 36591786›Full record

ArticleCirculation2023

Targeting Epsins to Inhibit Fibroblast Growth Factor Signaling While Potentiating Transforming Growth Factor-β Signaling Constrains Endothelial-to-Mesenchymal Transition in Atherosclerosis.

Yunzhou Dong, Beibei Wang, Mulong Du, Bo Zhu, Kui Cui, Kathryn Li, Ke Yuan, Douglas B Cowan, Sudarshan Bhattacharjee, Scott Wong and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in Circulation, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
8.9field-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

44 citing papers in PubMed, 54 citations in OpenAlex.

  1. Article
  2. Article
  3. Endothelial Elavl1 Fine-Tunes Immune Responses in Atherosclerosis.Arteriosclerosis, thrombosis, and vascular biology · 2026
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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

16 authors at 5 institutions in 1 country.

Yunzhou Dong *Vascular Biology Program (Y.D., B.W., B.Z., K. Cui, K.L., D.B.C., S.B., S.W., J.B., H.C.), Boston Children's Hospital, MA.
Beibei Wang *Vascular Biology Program (Y.D., B.W., B.Z., K. Cui, K.L., D.B.C., S.B., S.W., J.B., H.C.), Boston Children's Hospital, MA.
Mulong Du *Department of Environmental Health, Harvard T.H. Chan School of Public Health, Boston, MA (M.D.).
Bo ZhuVascular Biology Program (Y.D., B.W., B.Z., K. Cui, K.L., D.B.C., S.B., S.W., J.B., H.C.), Boston Children's Hospital, MA.
Kui CuiVascular Biology Program (Y.D., B.W., B.Z., K. Cui, K.L., D.B.C., S.B., S.W., J.B., H.C.), Boston Children's Hospital, MA.ORCID 0000-0003-2615-4932
Kathryn LiVascular Biology Program (Y.D., B.W., B.Z., K. Cui, K.L., D.B.C., S.B., S.W., J.B., H.C.), Boston Children's Hospital, MA.
Ke YuanDepartment of Medicine (K.Y.), Boston Children's Hospital, MA.
Douglas B CowanVascular Biology Program (Y.D., B.W., B.Z., K. Cui, K.L., D.B.C., S.B., S.W., J.B., H.C.), Boston Children's Hospital, MA.ORCID 0000-0002-6309-2737
Sudarshan BhattacharjeeVascular Biology Program (Y.D., B.W., B.Z., K. Cui, K.L., D.B.C., S.B., S.W., J.B., H.C.), Boston Children's Hospital, MA.
Scott WongVascular Biology Program (Y.D., B.W., B.Z., K. Cui, K.L., D.B.C., S.B., S.W., J.B., H.C.), Boston Children's Hospital, MA.
Jinjun ShiDepartment of Anesthesia (J.S.), Harvard Medical School, Boston, MA.ORCID 0000-0001-9200-5068
Da-Zhi WangUSF Heart Institute, Center for Regenerative Medicine, University of South Florida, Tampa (D.-Z.W.).
Kaifu ChenDepartment of Cardiology (K. Chen), Boston Children's Hospital, MA.ORCID 0000-0003-1009-4357
Joyce BischoffVascular Biology Program (Y.D., B.W., B.Z., K. Cui, K.L., D.B.C., S.B., S.W., J.B., H.C.), Boston Children's Hospital, MA.ORCID 0000-0002-6367-1974
MacRae F LintonDepartment of Medicine, Vanderbilt University Medical Center, Nashville, TN (M.F.L.).ORCID 0000-0002-9277-0453
Hong ChenVascular Biology Program (Y.D., B.W., B.Z., K. Cui, K.L., D.B.C., S.B., S.W., J.B., H.C.), Boston Children's Hospital, MA.ORCID 0000-0002-1906-6611
Boston Children's Hospital · USBrigham and Women's Hospital · USCalifornia Institute for Regenerative Medicine · USHarvard University · USVanderbilt University Medical Center · US

Funding

Epsin in Angiogenesis and Vascular RemodelingR01HL093242 · NHLBI · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI CHEN, HONG, WANG, DA-ZHI · 2009 to 2021
$7.3M
Molecular Mechanisms Controlling Lymphatic Vascular Function in Health and DiseaseR01HL133216 · NHLBI · BOSTON CHILDREN'S HOSPITAL · PI CHEN, HONG, DIXON, JAMES BRANDON · 2016 to 2025
$6.7M
Mechanisms regulating VEGF receptors in diabetic angiogenesisR01HL130845 · NHLBI · BOSTON CHILDREN'S HOSPITAL · PI CHEN, HONG, XU, JIAN · 2016 to 2023
$4.9M
Molecular Regulation of AtherosclerosisR01HL146134 · NHLBI · BOSTON CHILDREN'S HOSPITAL · PI CHEN, HONG, SRIVASTAVA, SANJAY · 2019 to 2022
$3.3M
CD45-mediated endothelial-to-mesenchymal transition in cardiovascular diseaseR01HL141853 · NHLBI · BOSTON CHILDREN'S HOSPITAL · PI CHEN, HONG, WANG, DA-ZHI · 2020 to 2023
$3.3M
The role of signaling adaptor protein epsin in atherosclerosisR01HL156362 · NHLBI · BOSTON CHILDREN'S HOSPITAL · PI CHEN, HONG, SHI, JINJUN · 2021 to 2024
$3.1M
Molecular Mechanisms Regulating Neuropilin 2 in LymphangiogenesisR01HL141858 · NHLBI · BOSTON CHILDREN'S HOSPITAL · PI BIELENBERG, DIANE RENEE, CHEN, HONG · 2019 to 2022
$3.1M
The Role of Adaptor Protein Disabled-2 in Maintaining Endothelial Cell Function in AtherosclerosisR01HL162367 · NHLBI · BOSTON CHILDREN'S HOSPITAL · PI CHEN, HONG, SHI, JINJUN · 2022 to 2025
$3.0M
Molecular Mechanisms Governing Vascular Cell Function and Phenotype in Health and DiseaseR01HL158097 · NHLBI · BOSTON CHILDREN'S HOSPITAL · PI CHEN, HONG, CHEN, YABING · 2021 to 2024
$3.0M
Reversal of Heart Failure: Role of Vascular RecoveryR01HL148338 · NHLBI · METHODIST HOSPITAL RESEARCH INSTITUTE · PI CHEN, KAIFU, COOKE, JOHN P · 2020 to 2023
$2.8M
Role of PXR in drug-elicited cardiovascular diseaseR01HL167206 · NHLBI · UNIVERSITY OF CALIFORNIA RIVERSIDE · PI Hong Chen, Changcheng Zhou · 2023 to 2026
$2.8M
Molecular Mechanisms Regulating Endothelial DysfunctionR01HL137229 · NHLBI · BOSTON CHILDREN'S HOSPITAL · PI CHEN, HONG, SRIVASTAVA, SANJAY · 2017 to 2020
$2.7M
BLRD VA I01 BX004426NHLBI NIH HHS R01 HL093242NHLBI NIH HHS R01 HL118676NHLBI NIH HHS R01 HL130845NHLBI NIH HHS R01 HL133216NHLBI NIH HHS R01 HL133254NHLBI NIH HHS R01 HL137229NHLBI NIH HHS R01 HL141853NHLBI NIH HHS R01 HL146134NHLBI NIH HHS R01 HL148338NHLBI NIH HHS R01 HL150106NHLBI NIH HHS R01 HL156362NHLBI NIH HHS R01 HL158097NHLBI NIH HHS R01 HL162367NHLBI NIH HHS R01 HL167206NIGMS NIH HHS R01 GM125632NIGMS NIH HHS R01 GM138407
6 · The paper itself

Abstract

backgroundEpsin endocytic adaptor proteins are implicated in the progression of atherosclerosis; however, the underlying molecular mechanisms have not yet been fully defined. In this study, we determined how epsins enhance endothelial-to-mesenchymal transition (EndoMT) in atherosclerosis and assessed the efficacy of a therapeutic peptide in a preclinical model of this disease.

methodsUsing single-cell RNA sequencing combined with molecular, cellular, and biochemical analyses, we investigated the role of epsins in stimulating EndoMT using knockout in

resultsSingle-cell RNA sequencing and lineage tracing revealed that epsins 1 and 2 promote EndoMT and that the loss of endothelial epsins inhibits EndoMT marker expression and transforming growth factor-β signaling in vitro and in atherosclerotic mice, which is associated with smaller lesions in the

conclusionsWe conclude that epsins potentiate EndoMT during atherogenesis by increasing transforming growth factor-β signaling through fibroblast growth factor receptor-1 internalization and degradation. Inhibition of EndoMT by reducing epsin-fibroblast growth factor receptor-1 interaction with a therapeutic peptide may represent a novel treatment strategy for atherosclerosis.

Indexed as

AtherosclerosisTransforming Growth Factor betaAdaptor Proteins, Vesicular TransportAnimalsApolipoproteins EFibroblast Growth FactorsMiceReceptors, Fibroblast Growth FactorTransforming Growth FactorsUbiquitinsAdaptor Proteins, Vesicular TransportApolipoproteins EepsinFibroblast Growth FactorsReceptors, Fibroblast Growth FactorTransforming Growth Factor betaTransforming Growth FactorsUbiquitinsadaptor proteins, signal transducingatherosclerosisendocytosisEndoMTepsinpeptidesreceptor, fibroblast growth factor, type 1single-cell gene expression analysistransforming growth factor betavascular diseases

Identifiers

PMID36591786
PMCPMC10136057
OpenAlexW4313424550

What OpenQuestion holds

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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.