Evidence map›Paper›PMID 26024305›Full record

ArticleScientific reports2015

A novel inhibitory mechanism of MRTF-A/B on the ICAM-1 gene expression in vascular endothelial cells.

Ken'ichiro Hayashi, Toshiyuki Murai, Hiroki Oikawa, Tomoyuki Masuda, Kazuhiro Kimura, Susanne Muehlich, Ron Prywes, Tsuyoshi Morita

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
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

17 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. SARS-CoV-2 and the Nucleus.International journal of biological sciences · 2022
    Review
  6. Nuclear Actin Dynamics in Gene Expression, DNA Repair, and Cancer.Results and problems in cell differentiation · 2022
    Article
  7. Article
  8. Effects of forces on chromatin.APL bioengineering · 2021
    Review
  9. Article
  10. MRTF: Basic Biology and Role in Kidney Disease.International journal of molecular sciences · 2021
    Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. 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

8 authors at 5 institutions in 3 countries.

Ken'ichiro HayashiDepartment of RNA Biology and Neuroscience, Osaka University Graduate School of Medicine, Suita, Osaka 565-0871, Japan.
Toshiyuki MuraiDepartment of RNA Biology and Neuroscience, Osaka University Graduate School of Medicine, Suita, Osaka 565-0871, Japan.
Hiroki OikawaDepartment of Pathology, School of Medicine, Iwate Medical University, Yahaba-Cho, Shiwa-Gun, Iwate 028-3694, Japan.
Tomoyuki MasudaDepartment of Pathology, School of Medicine, Iwate Medical University, Yahaba-Cho, Shiwa-Gun, Iwate 028-3694, Japan.
Kazuhiro KimuraDepartment of Ophthalmology, Yamaguchi University Graduate School of Medicine, Ube, Yamaguchi, 755-8505, Japan.
Susanne MuehlichWalther Straub Institute of Pharmacology and Toxicology, Ludwig-Maximilians-University, Munich, Germany.
Ron PrywesDepartment of Biological Sciences, Columbia University, New York, USA.
Tsuyoshi MoritaDepartment of RNA Biology and Neuroscience, Osaka University Graduate School of Medicine, Suita, Osaka 565-0871, Japan.
Osaka University · JPIwate Medical University · JPColumbia University · USLudwig-Maximilians-Universität München · DEYamaguchi University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The roles of myocardin-related transcription factor A (MRTF-A) and MRTF-B in vascular endothelial cells are not completely understood. Here, we found a novel regulatory mechanism for MRTF-A/B function. MRTF-A/B tend to accumulate in the nucleus in arterial endothelial cells in vivo and human aortic endothelial cells (HAoECs) in vitro. In HAoECs, nuclear localization of MRTF-A/B was not significantly affected by Y27632 or latrunculin B, primarily due to the reduced binding of MRTF-A/B to G-actin and in part, to the low level of MRTF-A phosphorylation by ERK. MRTF-A/B downregulation by serum depletion or transfection of siRNA against MRTF-A and/or MRTF-B induced ICAM-1 expression in HAoECs. It is known that nuclear import of nuclear factor-κB (NF-κB) plays a key role in ICAM-1 gene transcription. However, nuclear accumulation of NF-κB p65 was not observed in MRTF-A/B-depleted HAoECs. Our present findings suggest that MRTF-A/B inhibit ICAM-1 mRNA expression by forming a complex with NF-κB p65 in the nucleus. Conversely, downregulation of MRTF-A/B alleviates this negative regulation without further translocation of NF-κB p65 into the nucleus. These results reveal the novel roles of MRTF-A/B in the homeostasis of vascular endothelium.

Indexed as

Gene Expression RegulationAmidesAnimalsCell CommunicationCell LineCell NucleusEndothelial CellsExtracellular Signal-Regulated MAP KinasesHumansIntercellular Adhesion Molecule-1Intracellular SpaceLeukocytesLipopolysaccharidesMiceModels, BiologicalNF-kappa BAmidesExtracellular Signal-Regulated MAP KinasesIntercellular Adhesion Molecule-1LipopolysaccharidesMrtfa protein, mousemyocardin-related transcription factor B, mouseNF-kappa BPyridinesTrans-ActivatorsTranscription FactorsTumor Necrosis Factor-alphaY 27632

Identifiers

PMID26024305
PMCPMC4448521
OpenAlexW2271598438

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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.