Evidence map›Paper›PMID 27088725›Full record

ArticlePloS one2016

Redox-Sensitive Regulation of Myocardin-Related Transcription Factor (MRTF-A) Phosphorylation via Palladin in Vascular Smooth Muscle Cell Differentiation Marker Gene Expression.

Minyoung Lee, Alejandra San Martín, Alejandra Valdivia, Abel Martin-Garrido, Kathy K Griendling

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

16 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Nox4 Maintains Blood Pressure during Low Sodium Diet.Antioxidants (Basel, Switzerland) · 2021
    Article
  8. MRTF: Basic Biology and Role in Kidney Disease.International journal of molecular sciences · 2021
    Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. 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

5 authors at 1 institution in 1 country.

Minyoung LeeDepartment of Medicine, Division of Cardiology, Emory University, Atlanta, Georgia, United Sates of America.
Alejandra San MartínDepartment of Medicine, Division of Cardiology, Emory University, Atlanta, Georgia, United Sates of America.
Alejandra ValdiviaDepartment of Medicine, Division of Cardiology, Emory University, Atlanta, Georgia, United Sates of America.
Abel Martin-GarridoDepartment of Medicine, Division of Cardiology, Emory University, Atlanta, Georgia, United Sates of America.
Kathy K GriendlingDepartment of Medicine, Division of Cardiology, Emory University, Atlanta, Georgia, United Sates of America.
Emory University · US

Funding

T cell triggering events and hypertensionP01HL095070 · NHLBI · EMORY UNIVERSITY · PI JO, HANJOONG · 2009 to 2019
$20.5M
NOX4 and vascular smooth muscle differentiationR37HL038206 · NHLBI · EMORY UNIVERSITY · PI GRIENDLING, KATHY K · 2006 to 2015
$3.8M
VASCULAR SMOOTH MUSCLE PHOSPHOLIPASE DR01HL038206 · NHLBI · EMORY UNIVERSITY · PI GRIENDLING, KATHY K · 1993 to 2005
$2.1M
Mechanically Stressed VSMC: A Role for Slingshot Phosphatase in InflammationR01HL113167 · NHLBI · EMORY UNIVERSITY · PI SAN MARTIN, ALEJANDRA · 2013 to 2017
$1.9M
NHLBI NIH HHS P01 HL095070NHLBI NIH HHS P01HL095070NHLBI NIH HHS R01 HL038206NHLBI NIH HHS R01 HL113167NHLBI NIH HHS R01HL113167NHLBI NIH HHS R01HL38206NHLBI NIH HHS R37 HL038206
6 · The paper itself

Abstract

Vascular smooth muscle cells (VSMCs) undergo a phenotypic switch from a differentiated to synthetic phenotype in cardiovascular diseases such as atherosclerosis and restenosis. Our previous studies indicate that transforming growth factor-β (TGF-β) helps to maintain the differentiated phenotype by regulating expression of pro-differentiation genes such as smooth muscle α-actin (SMA) and Calponin (CNN) through reactive oxygen species (ROS) derived from NADPH oxidase 4 (Nox4) in VSMCs. In this study, we investigated the relationship between Nox4 and myocardin-related transcription factor-A (MRTF-A), a transcription factor known to be important in expression of smooth muscle marker genes. Previous work has shown that MRTF-A interacts with the actin-binding protein, palladin, although how this interaction affects MRTF-A function is unclear, as is the role of phosphorylation in MRTF-A activity. We found that Rho kinase (ROCK)-mediated phosphorylation of MRTF-A is a key event in the regulation of SMA and CNN in VSMCs and that this phosphorylation depends upon Nox4-mediated palladin expression. Knockdown of Nox4 using siRNA decreases TGF-β -induced palladin expression and MRTF-A phosphorylation, suggesting redox-sensitive regulation of this signaling pathway. Knockdown of palladin also decreases MRTF-A phosphorylation. These data suggest that Nox4-dependent palladin expression and ROCK regulate phosphorylation of MRTF-A, a critical factor in the regulation of SRF responsive gene expression.

Indexed as

ActinsCalcium-Binding ProteinsCalponinsCell DifferentiationCells, CulturedCytoskeletal ProteinsGene Expression RegulationGenetic MarkersHumansMicrofilament ProteinsMuscle, Smooth, VascularNADPH Oxidase 4NADPH OxidasesOxidation-ReductionPhosphoproteinsPhosphorylationACTA2 protein, humanActinsCalcium-Binding ProteinsCalponinsCytoskeletal ProteinsGenetic MarkersMicrofilament ProteinsMRTFA protein, humanNADPH Oxidase 4NADPH OxidasesNOX4 protein, humanPALLD protein, humanPhosphoproteinsrho-Associated KinasesTrans-ActivatorsTransforming Growth Factor beta

Identifiers

PMID27088725
PMCPMC4835087
OpenAlexW2340544421

What OpenQuestion holds

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LicenceCC BY
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.