Evidence map›Paper›PMID 30297530›Full record

ArticleThe EMBO journal2018

Distinct roles of VE-cadherin for development and maintenance of specific lymph vessel beds.

René Hägerling, Esther Hoppe, Cathrin Dierkes, Martin Stehling, Taija Makinen, Stefan Butz, Dietmar Vestweber, Friedemann Kiefer

Open access · bronzeAbstract read
In one paragraph

Article in The EMBO journal, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed
3.9field-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

61 citing papers in PubMed, 79 citations in OpenAlex.

  1. Article
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  3. Role of neutrophils in regulating vascular permeability in inflammatory and autoimmune diseases.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
    Review
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  8. Transport functions of intestinal lymphatic vessels.Nature reviews. Gastroenterology & hepatology · 2025
    Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Heliyon · 2024
    Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Developmental progression of lymphatic valve morphology and function.Frontiers in cell and developmental biology · 2024
    Article

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

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

8 authors at 3 institutions in 2 countries.

René HägerlingMammalian Cell Signaling Laboratory, Max Planck Institute for Molecular Biomedicine, Münster, Germany.
Esther HoppeMammalian Cell Signaling Laboratory, Max Planck Institute for Molecular Biomedicine, Münster, Germany.ORCID 0000-0001-7630-4535
Cathrin DierkesMammalian Cell Signaling Laboratory, Max Planck Institute for Molecular Biomedicine, Münster, Germany.
Martin StehlingFlow Cytometry Unit, Max Planck Institute for Molecular Biomedicine, Münster, Germany.
Taija MakinenDepartment of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.
Stefan ButzDepartment Vascular Cell Biology, Max Planck Institute for Molecular Biomedicine, Münster, Germany.
Dietmar VestweberDepartment Vascular Cell Biology, Max Planck Institute for Molecular Biomedicine, Münster, Germany.
Friedemann KieferMammalian Cell Signaling Laboratory, Max Planck Institute for Molecular Biomedicine, Münster, Germany fkiefer@gwdg.de.ORCID 0000-0002-3002-8237
Max Planck Institute for Molecular Biomedicine · DEUniversity of Münster · DEUppsala University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Endothelial cells line blood and lymphatic vessels and form intercellular junctions, which preserve vessel structure and integrity. The vascular endothelial cadherin, VE-cadherin, mediates endothelial adhesion and is indispensible for blood vessel development and permeability regulation. However, its requirement for lymphatic vessels has not been addressed. During development, VE-cadherin deletion in lymphatic endothelial cells resulted in abortive lymphangiogenesis, edema, and prenatal death. Unexpectedly, inducible postnatal or adult deletion elicited vessel bed-specific responses. Mature dermal lymph vessels resisted VE-cadherin loss and maintained button junctions, which was associated with an upregulation of junctional molecules. Very different, mesenteric lymphatic collectors deteriorated and formed a strongly hyperplastic layer of lymphatic endothelial cells on the mesothelium. This massive hyperproliferation may have been favored by high mesenteric VEGF-C expression and was associated with VEGFR-3 phosphorylation and upregulation of the transcriptional activator TAZ Finally, intestinal lacteals fragmented into cysts or became highly distended possibly as a consequence of the mesenteric defects. Taken together, we demonstrate here the importance of VE-cadherin for lymphatic vessel development and maintenance, which is however remarkably vessel bed-specific.

Indexed as

Gene Expression Regulation, DevelopmentalLymphangiogenesisAnimalsAntigens, CDCadherin 5CadherinsDermisEndothelial CellsGene DeletionLymphatic VesselsMesenteryMiceVascular Endothelial Growth Factor CVascular Endothelial Growth Factor Receptor-3Antigens, CDCadherin 5CadherinsVascular Endothelial Growth Factor Cvascular endothelial growth factor C, mouseVascular Endothelial Growth Factor Receptor-3lymphatic valveslymph vesselsvascular heterogeneityVE‐cadherinYAP/TAZ

Identifiers

PMID30297530
PMCPMC6236332
OpenAlexW2897748929

What OpenQuestion holds

Textmetadata
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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.