Evidence map›Paper›PMID 20716773›Full record

ArticleBlood2010

Podoplanin-Fc reduces lymphatic vessel formation in vitro and in vivo and causes disseminated intravascular coagulation when transgenically expressed in the skin.

Leah N Cueni, Lu Chen, Hui Zhang, Daniela Marino, Reto Huggenberger, Annamari Alitalo, Roberta Bianchi, Michael Detmar

Abstract read
In one paragraph

Article in Blood, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
–field-weighted citation impact
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

29 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Podoplanin in Inflammation and Cancer.International journal of molecular sciences · 2019
    Review
  11. Phenotypic transformation of intimal and adventitial lymphatics in atherosclerosis: a regulatory role for soluble VEGF receptor 2.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2016
    Article
  12. Article
  13. Article
  14. Podoplanin - a small glycoprotein with many faces.American journal of cancer research · 2016
    Review
  15. Article
  16. Podoplanin--a novel marker in oral carcinogenesis.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2014
    Review
  17. Article
  18. Article
  19. Investigation of biomarker in laryngeal carcinomas.Journal of clinical laboratory analysis · 2014
    Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Leah N CueniInstitute of Pharmaceutical Sciences, Swiss Federal Institute of Technology, ETH Zurich, Zurich, Switzerland.
Lu Chen
Hui Zhang
Daniela Marino
Reto Huggenberger
Annamari Alitalo
Roberta Bianchi
Michael Detmar

Funding

Molecular Regulation of Lymphangiogenesis in Corneal AlloimmunityR01EY017392 · NEI · UNIVERSITY OF CALIFORNIA BERKELEY · PI CHEN, LU · 2007 to 2020
$5.7M
VPF/VEGF IN NORMAL AND NEOPLASTIC SKIN ANGIOGENESISR01CA069184 · NCI · SWISS FEDERAL INST OF TECH (ETH ZURICH) · PI DETMAR, MICHAEL J. · 1996 to 2008
$1.6M
NCI NIH HHS CA69184NCI NIH HHS R01 CA069184NEI NIH HHS EY17392NEI NIH HHS R01 EY017392
6 · The paper itself

Abstract

Podoplanin is a small transmembrane protein required for development and function of the lymphatic vascular system. To investigate the effects of interfering with its function, we produced an Fc fusion protein of its ectodomain. We found that podoplanin-Fc inhibited several functions of cultured lymphatic endothelial cells and also specifically suppressed lymphatic vessel growth, but not blood vessel growth, in mouse embryoid bodies in vitro and in mouse corneas in vivo. Using a keratin 14 expression cassette, we created transgenic mice that overexpressed podoplanin-Fc in the skin. No obvious outward phenotype was identified in these mice, but surprisingly, podoplanin-Fc-although produced specifically in the skin-entered the blood circulation and induced disseminated intravascular coagulation, characterized by microthrombi in most organs and by thrombocytopenia, occasionally leading to fatal hemorrhage. These findings reveal an important role of podoplanin in lymphatic vessel formation and indicate the potential of podoplanin-Fc as an inhibitor of lymphangiogenesis. These results also demonstrate the ability of podoplanin to induce platelet aggregation in vivo, which likely represents a major function of lymphatic endothelium. Finally, keratin 14 podoplanin-Fc mice represent a novel genetic animal model of disseminated intravascular coagulation.

Indexed as

AnimalsBlood CoagulationBlood PlateletsCell AdhesionCell LineCell MovementCorneaDisseminated Intravascular CoagulationEmbryoid BodiesEndothelial CellsHumansInflammationKeratin-14LymphangiogenesisLymphatic VesselsMembrane GlycoproteinsKeratin-14Membrane GlycoproteinsPDPN protein, humanPodoplaninReceptors, FcRecombinant Fusion Proteins

Identifiers

PMID20716773
PMCPMC2993634

What OpenQuestion holds

Textmetadata
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.