Evidence map›Paper›PMID 19674970›Full record

ArticleThe Journal of biological chemistry2009

Critical role for GATA3 in mediating Tie2 expression and function in large vessel endothelial cells.

Haihua Song, Jun-ichi Suehiro, Yasuharu Kanki, Yoshiko Kawai, Kenji Inoue, Hiroyuki Daida, Kiichiro Yano, Toshio Ohhashi, Peter Oettgen, William C Aird and 2 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed, 3 pooled it
2.2field-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

47 citing papers in PubMed, 3 syntheses or guidelines pooled it, 78 citations in OpenAlex.

  1. Pooled it
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    Pooled it
  3. Pooled it
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  12. Transcription factors regulating vasculogenesis and angiogenesis.Developmental dynamics : an official publication of the American Association of Anatomists · 2024
    Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
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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

12 authors at 5 institutions in 2 countries.

Haihua SongResearch Center for Advanced Science and Technology, The University of Tokyo, Tokyo 153-8904, Japan.
Jun-ichi Suehiro
Yasuharu Kanki
Yoshiko Kawai
Kenji Inoue
Hiroyuki Daida
Kiichiro Yano
Toshio Ohhashi
Peter Oettgen
William C Aird
Tatsuhiko Kodama
Takashi Minami
The University of Tokyo · JPBeth Israel Deaconess Medical Center · USJuntendo University · JPShinshu University · JPHarvard University · US

Funding

VASCULAR TOPOGRAPHY OF CD39/NTPDASESP01HL076540 · NHLBI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI MARSDEN, PHILIP · 2004 to 2014
$20.3M
VEGF, Transcriptional Networks and Vascular InflammationR01HL082927 · NHLBI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI AIRD, WILLIAM C · 2007 to 2010
$1.5M
NHLBI NIH HHS P01 HL076540NHLBI NIH HHS P01 HL76540NHLBI NIH HHS R01 HL082927NHLBI NIH HHS R01HL082927
6 · The paper itself

Abstract

Endothelial phenotypes are highly regulated in space and time by both transcriptional and post-transcriptional mechanisms. There is increasing evidence that the GATA family of transcription factors function as signal transducers, coupling changes in the extracellular environment to changes in downstream target gene expression. Here we show that human primary endothelial cells derived from large blood vessels express GATA2, -3, and -6. Of these factors, GATA3 was expressed at the highest levels. In DNA microarrays of human umbilical vein endothelial cells (HUVEC), small interfering RNA-mediated knockdown of GATA3 resulted in reduced expression of genes associated with angiogenesis, including Tie2. At a functional level, GATA3 knockdown inhibited angiopoietin (Ang)-1-mediated but not vascular endothelial cell growth factor (VEGF)-mediated AKT signaling, cell migration, survival, and tube formation. In electrophoretic gel mobility shift assays and chromatin immunoprecipitation, GATA3 was shown to bind to regulatory regions within the 5'-untranslated region of the Tie2 gene. In co-immunoprecipitation and co-transfection assays, GATA3 and the Ets transcription factor, ELF1, physically interacted and synergized to transactivate the Tie2 promoter. GATA3 knockdown blocked the ability of Ang-1 to attenuate vascular endothelial cell growth factor stimulation of vascular cell adhesion molecule-1 expression and monocytic cell adhesion. Moreover, exposure of human umbilical vein endothelial cells to tumor necrosis factor-alpha resulted in marked down-regulation of GATA3 expression and reduction in Tie2 expression. Together, these findings suggest that GATA3 is indispensable for Ang-1-Tie2-mediated signaling in large vessel endothelial cells.

Indexed as

Gene Expression RegulationAngiopoietin-1Endothelial CellsEndothelium, VascularGATA3 Transcription FactorHumansImmunoprecipitationOligonucleotide Array Sequence AnalysisPhenotypePromoter Regions, GeneticReceptor, TIE-2RNA, Small InterferingTumor Necrosis Factor-alphaUmbilical VeinsVascular Endothelial Growth Factor AAngiopoietin-1GATA3 protein, humanGATA3 Transcription FactorReceptor, TIE-2RNA, Small InterferingTumor Necrosis Factor-alphaVascular Endothelial Growth Factor A

Identifiers

PMID19674970
PMCPMC2781456
OpenAlexW2017165199

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.