Evidence map›Paper›PMID 23603512›Full record

ArticleCirculation research2013

Regulation of vascular smooth muscle cell turnover by endothelial cell-secreted microRNA-126: role of shear stress.

Jing Zhou, Yi-Shuan Li, Phu Nguyen, Kuei-Chun Wang, Anna Weiss, Yi-Chun Kuo, Jeng-Jiann Chiu, John Y Shyy, Shu Chien

Open access · bronzeAbstract read
In one paragraph

Article in Circulation research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 138 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
138citing papers in PubMed, 2 pooled it
10.3field-weighted citation impact, top 1% 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

138 citing papers in PubMed, 2 syntheses or guidelines pooled it, 251 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
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  12. MicroRNA-126 (MiR-126): key roles in related diseases.Journal of physiology and biochemistry · 2024
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Endothelial mechanobiology in atherosclerosis.Cardiovascular research · 2023
    Review
  19. Roles of non-coding RNAs in intercellular crosstalk in cardiovascular diseases.The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2023
    Review
  20. Article

78 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 1 institution in 2 countries.

Jing ZhouDepartment of Bioengineering and Institute of Engineering in Medicine, University of California, San Diego, La Jolla, CA 92093, USA.
Yi-Shuan Li
Phu Nguyen
Kuei-Chun Wang
Anna Weiss
Yi-Chun Kuo
Jeng-Jiann Chiu
John Y Shyy
Shu Chien
National Yang Ming Chiao Tung University · TW

Funding

Systems Biology Analyses for Hemodynamic Regulation of Vascular HomeostasisR01HL108735 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI CHIEN, SHU, SHYY, JOHN YJ · 2012 to 2024
$13.4M
Shear Regulation of MicroRNA Transportomes and Targetomes in Vascular HomeostasisR01HL106579 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI CHIEN, SHU, SHYY, JOHN YJ · 2011 to 2022
$8.3M
Shear Stress, AMPK, and Endothelial FunctionsR01HL089940 · NHLBI · UNIVERSITY OF CALIFORNIA RIVERSIDE · PI SHYY, JOHN YJ · 2009 to 2013
$1.9M
NHLBI NIH HHS HL106579NHLBI NIH HHS HL108735NHLBI NIH HHS HL89940NHLBI NIH HHS R01 HL089940NHLBI NIH HHS R01 HL106579NHLBI NIH HHS R01 HL108735
6 · The paper itself

Abstract

rationaleEndothelial microRNA-126 (miR-126) modulates vascular development and angiogenesis. However, its role in the regulation of smooth muscle cell (SMC) function is unknown.

objectiveTo elucidate the role of miR-126 secreted by endothelial cells (ECs) in regulating SMC turnover in vitro and in vivo, as well as the effects of shear stress on the regulation. METHODS AND

resultsCoculture of SMCs with ECs or treatment of SMCs with conditioned media from static EC monoculture (EC-CM) increased SMC miR-126 level and SMC turnover; these effects were abolished by inhibition of endothelial miR-126 and by the application of laminar shear stress to ECs. SMC miR-126 did not increase when treated with EC-CM from ECs subjected to inhibition of miR biogenesis, or with CM from sheared ECs. Depletion of extracellular/secreted vesicles in EC-CM did not affect the increase of SMC miR-126 by EC-CM. Biotinylated miR-126 or FLAG (DYKDDDDK epitope)-tagged Argonaute2 transfected into ECs was detected in the cocultured or EC-CM-treated SMCs, indicating a direct EC-to-SMC transmission of miR-126 and Argonaute2. Endothelial miR-126 represses forkhead box O3, B-cell lymphoma 2, and insulin receptor substrate 1 mRNAs in the cocultured SMCs, suggesting the functional roles of the transmitted miR-126. Systemic depletion of miR-126 in mice inhibited neointimal lesion formation of carotid arteries induced by cessation of blood flow. Administration of EC-CM or miR-126 mitigated the inhibitory effect.

conclusionsEndothelial miR-126 acts as a key intercellular mediator to increase SMC turnover, and its release is reduced by atheroprotective laminar shear stress.

Indexed as

Gene Expression RegulationAnimalsArgonaute ProteinsCarotid Artery, CommonCell Culture TechniquesCell LineCoculture TechniquesCulture Media, ConditionedEndothelial CellsForkhead Box Protein O3Forkhead Transcription FactorsGenes, bcl-2Gene SilencingHemorheologyHumansHuman Umbilical Vein Endothelial CellsAGO2 protein, humanArgonaute ProteinsCulture Media, ConditionedForkhead Box Protein O3Forkhead Transcription FactorsFOXO3 protein, humanInsulin Receptor Substrate ProteinsIRS1 protein, humanMicroRNAsMIRN126 microRNA, humanMIRN126 microRNA, mouseProto-Oncogene Proteins c-bcl-2Recombinant Fusion Proteinsatherosclerosisendothelial cellextracellular miR-126shear stresssmooth muscle cell

Identifiers

PMID23603512
PMCPMC3772783
OpenAlexW2110973939

What OpenQuestion holds

Textmetadata
LicenceTDM
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.