Evidence map›Paper›PMID 30295643›Full record

ArticleThe Journal of clinical investigation2018

Angiopoietin-2 exacerbates cardiac hypoxia and inflammation after myocardial infarction.

Seung-Jun Lee, Choong-Kun Lee, Seok Kang, Intae Park, Yoo Hyung Kim, Seo Ki Kim, Seon Pyo Hong, Hosung Bae, Yulong He, Yoshiaki Kubota and 1 more

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 103 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
103citing papers in PubMed, 1 pooled it
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

103 citing papers in PubMed, 1 synthesis or guideline pooled it, 153 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Molecular Mechanisms Governing Vascular Function in Heart Failure.Arteriosclerosis, thrombosis, and vascular biology · 2026
    Review
  4. Review
  5. Review
  6. Review
  7. LncRNAiScience · 2026
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Cellular and molecular signals of cardiac wound healing after myocardial infarction.American journal of physiology. Heart and circulatory physiology · 2026
    Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Article

43 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 3 institutions in 3 countries.

Seung-Jun LeeCenter for Vascular Research, Institute for Basic Science, Daejeon, South Korea.
Choong-Kun LeeCenter for Vascular Research, Institute for Basic Science, Daejeon, South Korea.
Seok KangCenter for Vascular Research, Institute for Basic Science, Daejeon, South Korea.
Intae ParkCenter for Vascular Research, Institute for Basic Science, Daejeon, South Korea.
Yoo Hyung KimCenter for Vascular Research, Institute for Basic Science, Daejeon, South Korea.
Seo Ki KimCenter for Vascular Research, Institute for Basic Science, Daejeon, South Korea.
Seon Pyo HongCenter for Vascular Research, Institute for Basic Science, Daejeon, South Korea.
Hosung BaeCenter for Vascular Research, Institute for Basic Science, Daejeon, South Korea.
Yulong HeCyrus Tang Hematology Center, Soochow University, Suzhou, China.
Yoshiaki KubotaThe Laboratory of Vascular Biology, School of Medicine, Keio University, Tokyo, Japan.
Gou Young KohCenter for Vascular Research, Institute for Basic Science, Daejeon, South Korea.
Korea Advanced Institute of Science and Technology · KRInstitute for Basic Science · KRKeio University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Emerging evidence indicates that angiopoietin-2 (Angpt2), a well-recognized vascular destabilizing factor, is a biomarker of poor outcome in ischemic heart disease. However, its precise role in postischemic cardiovascular remodeling is poorly understood. Here, we show that Angpt2 plays multifaceted roles in the exacerbation of cardiac hypoxia and inflammation after myocardial ischemia. Angpt2 was highly expressed in endothelial cells at the infarct border zone after myocardial infarction (MI) or ischemia/reperfusion injury in mice. In the acute phase of MI, endothelial-derived Angpt2 antagonized Angpt1/Tie2 signaling, which was greatly involved in pericyte detachment, vascular leakage, increased adhesion molecular expression, degradation of the glycocalyx and extracellular matrix, and enhanced neutrophil infiltration and hypoxia in the infarct border area. In the chronic remodeling phase after MI, endothelial- and macrophage-derived Angpt2 continuously promoted abnormal vascular remodeling and proinflammatory macrophage polarization through integrin α5β1 signaling, worsening cardiac hypoxia and inflammation. Accordingly, inhibition of Angpt2 either by gene deletion or using an anti-Angpt2 blocking antibody substantially alleviated these pathological findings and ameliorated postischemic cardiovascular remodeling. Blockade of Angpt2 thus has potential as a therapeutic option for ischemic heart failure.

Indexed as

Signal TransductionAngiopoietin-1Angiopoietin-2AnimalsAntibodies, BlockingEndothelial CellsInflammationMacrophagesMaleMiceMice, KnockoutMyocardial InfarctionReceptors, VitronectinReceptor, TIE-2Vascular RemodelingAngiopoietin-1Angiopoietin-2Angpt1 protein, mouseAntibodies, Blockingintegrin alphavbeta1Receptors, VitronectinReceptor, TIE-2Tek protein, mouseCardiologyCardiovascular diseaseendothelial cellsPericytesVascular Biology

Identifiers

PMID30295643
PMCPMC6205384
OpenAlexW2894621368

What OpenQuestion holds

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Read underepoch 390

Registered trials

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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.