Evidence map›Paper›PMID 25909848›Full record

ArticlePloS one2015

BMP9 Crosstalk with the Hippo Pathway Regulates Endothelial Cell Matricellular and Chemokine Responses.

Kira Young, Eric Tweedie, Barbara Conley, Jacquelyn Ames, MaryLynn FitzSimons, Peter Brooks, Lucy Liaw, Calvin P H Vary

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

28 citing papers in PubMed, 40 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. The effect of BMP9 on inflammation in the early stage of pulpitis.Journal of applied oral science : revista FOB · 2023
    Article
  5. Review
  6. The diverse functions of FAT1 in cancer progression: good, bad, or ugly?Journal of experimental & clinical cancer research : CR · 2022
    Review
  7. Article
  8. Endoglin in the Spotlight to Treat Cancer.International journal of molecular sciences · 2021
    Review
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Role of Hippo-YAP1/TAZ pathway and its crosstalk in cardiac biology.International journal of biological sciences · 2020
    Review
  17. Elevated BMP and Mechanical Signaling Through YAP1/RhoA Poises FOP Mesenchymal Progenitors for Osteogenesis.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2019
    Article
  18. Article
  19. Article
  20. Review
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 2 institutions in 1 country.

Kira YoungCenter for Molecular Medicine, Maine Medical Center Research Institute, Scarborough, Maine 04074, United States of America; Graduate School of Biomedical Sciences and Engineering, University of Maine, Orono, Maine 04469, United States of America.
Eric TweedieCenter for Molecular Medicine, Maine Medical Center Research Institute, Scarborough, Maine 04074, United States of America.
Barbara ConleyCenter for Molecular Medicine, Maine Medical Center Research Institute, Scarborough, Maine 04074, United States of America.
Jacquelyn AmesCenter for Molecular Medicine, Maine Medical Center Research Institute, Scarborough, Maine 04074, United States of America; Graduate School of Biomedical Sciences and Engineering, University of Maine, Orono, Maine 04469, United States of America.
MaryLynn FitzSimonsGraduate School of Biomedical Sciences and Engineering, University of Maine, Orono, Maine 04469, United States of America.
Peter BrooksCenter for Molecular Medicine, Maine Medical Center Research Institute, Scarborough, Maine 04074, United States of America; Graduate School of Biomedical Sciences and Engineering, University of Maine, Orono, Maine 04469, United States of America.
Lucy LiawCenter for Molecular Medicine, Maine Medical Center Research Institute, Scarborough, Maine 04074, United States of America; Graduate School of Biomedical Sciences and Engineering, University of Maine, Orono, Maine 04469, United States of America.
Calvin P H VaryCenter for Molecular Medicine, Maine Medical Center Research Institute, Scarborough, Maine 04074, United States of America; Graduate School of Biomedical Sciences and Engineering, University of Maine, Orono, Maine 04469, United States of America.
Maine Medical Center Research Institute · USUniversity of Maine · US

Funding

Progenitor Cell Analysis CoreP30GM106391 · NIGMS · MAINEHEALTH · PI WOJCHOWSKI, DON MICHAEL · 2013 to 2017
$5.7M
Phase III COBRE in Vascular BiologyP30GM103392 · NIGMS · MAINEHEALTH · PI ST. GERMAIN, DONALD L. · 2012 to 2016
$4.7M
Contribution of Notch Signaling to Vascular RemodelingR01HL070865 · NHLBI · MAINE MEDICAL CENTER · PI LIAW, LUCY · 2003 to 2017
$4.6M
CRYPTIC DOMAINS OF COLLAGEN IV IN TUMOR GROWTHR01CA091645 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI BROOKS, PETER C. · 2000 to 2011
$3.3M
Regulation of TGF-beta Receptor-dependent Vascular DiseaseR01HL083151 · NHLBI · MAINEHEALTH · PI VARY, CALVIN PARDEE HULL · 2007 to 2011
$2.0M
Smooth muscle cell integration of differentiation signalsR01HL109652 · NHLBI · MAINEHEALTH · PI LIAW, LUCY · 2012 to 2015
$1.5M
NCI NIH HHS CA91645NCI NIH HHS R01 CA091645NHLBI NIH HHS HL070865NHLBI NIH HHS HL083151NHLBI NIH HHS HL109652NHLBI NIH HHS R01 HL070865NHLBI NIH HHS R01 HL083151NHLBI NIH HHS R01 HL109652NIGMS NIH HHS 1P30 GM106391NIGMS NIH HHS P30 GM103392NIGMS NIH HHS P30GM103392NIGMS NIH HHS P30 GM106391
6 · The paper itself

Abstract

Endoglin is a type III TGFβ auxiliary receptor that is upregulated in endothelial cells during angiogenesis and, when mutated in humans, results in the vascular disease hereditary hemorrhagic telangiectasia (HHT). Though endoglin has been implicated in cell adhesion, the underlying molecular mechanisms are still poorly understood. Here we show endoglin expression in endothelial cells regulates subcellular localization of zyxin in focal adhesions in response to BMP9. RNA knockdown of endoglin resulted in mislocalization of zyxin and altered formation of focal adhesions. The mechanotransduction role of focal adhesions and their ability to transmit regulatory signals through binding of the extracellular matrix are altered by endoglin deficiency. BMP/TGFβ transcription factors, SMADs, and zyxin have recently been implicated in a newly emerging signaling cascade, the Hippo pathway. The Hippo transcription coactivator, YAP1 (yes-associated protein 1), has been suggested to play a crucial role in mechanotransduction and cell-cell contact. Identification of BMP9-dependent nuclear localization of YAP1 in response to endoglin expression suggests a mechanism of crosstalk between the two pathways. Suppression of endoglin and YAP1 alters BMP9-dependent expression of YAP1 target genes CCN1 (cysteine-rich 61, CYR61) and CCN2 (connective tissue growth factor, CTGF) as well as the chemokine CCL2 (monocyte chemotactic protein 1, MCP-1). These results suggest a coordinate effect of endoglin deficiency on cell matrix remodeling and local inflammatory responses. Identification of a direct link between the Hippo pathway and endoglin may reveal novel mechanisms in the etiology of HHT.

Indexed as

Signal TransductionAdaptor Proteins, Signal TransducingAnimalsAntigens, CDChemokine CCL2ChemokinesConnective Tissue Growth FactorCysteine-Rich Protein 61EndoglinEndothelial CellsExtracellular MatrixFocal AdhesionsGrowth Differentiation Factor 2Growth Differentiation FactorsHippo Signaling PathwayHumansAdaptor Proteins, Signal TransducingAntigens, CDCCN2 protein, humanCCR2 protein, humanChemokine CCL2ChemokinesConnective Tissue Growth FactorCysteine-Rich Protein 61EndoglinENG protein, humanGDF2 protein, humanGrowth Differentiation Factor 2Growth Differentiation FactorsPhosphoproteinsProtein Serine-Threonine KinasesReceptors, CCR2Receptors, Cell SurfaceSmad ProteinsTranscription FactorsYAP1 protein, humanYAP-Signaling ProteinsZyxin

Identifiers

PMID25909848
PMCPMC4409298
OpenAlexW2023404925

What OpenQuestion holds

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LicenceCC BY
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.