Evidence map›Paper›PMID 30150707›Full record

ArticleNature communications2018

NCK-dependent pericyte migration promotes pathological neovascularization in ischemic retinopathy.

Alexandre Dubrac, Steffen E Künzel, Sandrine H Künzel, Jinyu Li, Rachana Radhamani Chandran, Kathleen Martin, Daniel M Greif, Ralf H Adams, Anne Eichmann

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
3.5field-weighted citation impact, top 6% 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

57 citing papers in PubMed, 81 citations in OpenAlex.

  1. Article
  2. Proangiogenic effect and molecular mechanism of a new cytosporin derivative from the marine fungus Eutypella sp. D-1.Medicinal chemistry research : an international journal for rapid communications on design and mechanisms of action of biologically active agents · 2026
    Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. Eppur si muove: the dynamic brain pericyte.Fluids and barriers of the CNS · 2025
    Review
  8. Article
  9. Review
  10. Review
  11. Biglycan stimulates retinal pathological angiogenesis via up-regulation of CXCL12 expression in pericytes.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Pericytes in the disease spotlight.Trends in cell biology · 2024
    Review
  17. Impaired pericyte-Müller glia interactionInternational journal of ophthalmology · 2024
    Article
  18. Review
  19. Article
  20. Article
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 3 institutions in 3 countries.

Alexandre DubracDepartment of Internal Medicine, Yale Cardiovascular Research Center, Yale University School of Medicine, New Haven, CT, 06511, USA. alexandre.dubrac@yale.edu.ORCID http://orcid.org/0000-0002-3829-2577
Steffen E KünzelDepartment of Internal Medicine, Yale Cardiovascular Research Center, Yale University School of Medicine, New Haven, CT, 06511, USA.
Sandrine H KünzelDepartment of Internal Medicine, Yale Cardiovascular Research Center, Yale University School of Medicine, New Haven, CT, 06511, USA.
Jinyu LiDepartment of Internal Medicine, Yale Cardiovascular Research Center, Yale University School of Medicine, New Haven, CT, 06511, USA.
Rachana Radhamani ChandranDepartment of Internal Medicine, Yale Cardiovascular Research Center, Yale University School of Medicine, New Haven, CT, 06511, USA.
Kathleen MartinDepartment of Internal Medicine, Yale Cardiovascular Research Center, Yale University School of Medicine, New Haven, CT, 06511, USA.
Daniel M GreifDepartment of Internal Medicine, Yale Cardiovascular Research Center, Yale University School of Medicine, New Haven, CT, 06511, USA.
Ralf H AdamsDepartment of Tissue Morphogenesis and University of Münster, Faculty of Medicine, Max Planck Institute for Molecular Biomedicine, 48149, Münster, Germany.ORCID http://orcid.org/0000-0003-3031-7677
Anne EichmannDepartment of Internal Medicine, Yale Cardiovascular Research Center, Yale University School of Medicine, New Haven, CT, 06511, USA. anne.eichmann@yale.edu.
Yale University · USInserm · FRUniversity of Münster · DE

Funding

Yale Core Grant for Vision ResearchP30EY026878 · NEI · YALE UNIVERSITY · PI In-Jung Kim · 2016 to 2026
$7.1M
Novel targets of rapamycin and Akt in vascular smooth muscle cell differentiationR01HL091013 · NHLBI · YALE UNIVERSITY · PI MARTIN, KATHLEEN ANN · 2008 to 2017
$4.1M
Targeting endothelial migration to prevent neovascularizationR01HL125811 · NHLBI · YALE UNIVERSITY · PI EICHMANN, ANNE CHRISTINE · 2015 to 2025
$4.1M
Novel insights into intimal hyperplasia in cardiac allograft vasculopathyR01HL142090 · NHLBI · YALE UNIVERSITY · PI MARTIN, KATHLEEN ANN · 2018 to 2021
$2.4M
Novel approaches to manipulate sprouting angiogenesisR01EY025979 · NEI · YALE UNIVERSITY · PI EICHMANN, ANNE CHRISTINE · 2015 to 2019
$1.9M
Smooth muscle progenitors in vascular remodelingR01HL133016 · NHLBI · YALE UNIVERSITY · PI GREIF, DANIEL · 2016 to 2019
$1.7M
Pathological arterial muscularization and the role of integrinsR01HL125815 · NHLBI · YALE UNIVERSITY · PI GREIF, DANIEL · 2015 to 2018
$1.7M
Regulation of vascular smooth muscle cell plasticityR01HL118430 · NHLBI · YALE UNIVERSITY · PI MARTIN, KATHLEEN ANN · 2014 to 2017
$1.7M
Epigenetic control of vascular smooth muscle in cardiovascular diseaseR01HL119529 · NHLBI · YALE UNIVERSITY · PI MARTIN, KATHLEEN ANN · 2014 to 2017
$1.7M
Mural cell TGF-beta-mediated signaling and neonatal intracerebral hemorrhageR21NS088854 · NINDS · YALE UNIVERSITY · PI GREIF, DANIEL · 2014 to 2015
$458k
Agence Nationale de la Recherche (French National Research Agency) ANR Gandhi, BrainwashAmerican Heart Association (American Heart Association, Inc.) 17SDG33700124NEI NIH HHS P30 EY026878NEI NIH HHS R01 EY025979NHLBI NIH HHS R01 HL091013NHLBI NIH HHS R01 HL118430NHLBI NIH HHS R01 HL119529NHLBI NIH HHS R01 HL125811NHLBI NIH HHS R01 HL125815NHLBI NIH HHS R01 HL133016NHLBI NIH HHS R01 HL142090NINDS NIH HHS R21 NS088854U.S. Department of Health & Human Services | NIH | National Eye Institute (NEI) 5R01EY025979U.S. Department of Health & Human Services | NIH | National Heart, Lung, and Blood Institute (NHLBI) 1R01HL125815U.S. Department of Health & Human Services | NIH | National Heart, Lung, and Blood Institute (NHLBI) 1R01HL133016U.S. Department of Health & Human Services | NIH | National Heart, Lung, and Blood Institute (NHLBI) 5R01HL125811U.S. Department of Health & Human Services | NIH | National Institute of Neurological Disorders and Stroke (NINDS) R21NS088854
6 · The paper itself

Abstract

Pericytes are mural cells that surround capillaries and control angiogenesis and capillary barrier function. During sprouting angiogenesis, endothelial cell-derived platelet-derived growth factor-B (PDGF-B) regulates pericyte proliferation and migration via the platelet-derived growth factor receptor-β (PDGFRβ). PDGF-B overexpression has been associated with proliferative retinopathy, but the underlying mechanisms remain poorly understood. Here we show that abnormal, α-SMA-expressing pericytes cover angiogenic sprouts and pathological neovascular tufts (NVTs) in a mouse model of oxygen-induced retinopathy. Genetic lineage tracing demonstrates that pericytes acquire α-SMA expression during NVT formation. Pericyte depletion through inducible endothelial-specific knockout of Pdgf-b decreases NVT formation and impairs revascularization. Inactivation of the NCK1 and NCK2 adaptor proteins inhibits pericyte migration by preventing PDGF-B-induced phosphorylation of PDGFRβ at Y1009 and PAK activation. Loss of Nck1 and Nck2 in mural cells prevents NVT formation and vascular leakage and promotes revascularization, suggesting PDGFRβ-Y1009/NCK signaling as a potential target for the treatment of retinopathies.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsCell MovementDiabetic RetinopathyIschemiaMiceNeovascularization, PathologicOncogene ProteinsPericytesProto-Oncogene Proteins c-sisReceptor, Platelet-Derived Growth Factor betaSignal TransductionAdaptor Proteins, Signal TransducingNck2 protein, mouseNck proteinOncogene ProteinsProto-Oncogene Proteins c-sisReceptor, Platelet-Derived Growth Factor beta

Identifiers

PMID30150707
PMCPMC6110853
OpenAlexW2888429607

What OpenQuestion holds

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LicenceCC BY
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.