Evidence map›Paper›PMID 26065992›Full record

ArticleJournal of the American College of Cardiology2015

An Endocrine Genetic Signal Between Blood Cells and Vascular Smooth Muscle Cells: Role of MicroRNA-223 in Smooth Muscle Function and Atherogenesis.

Zhen Shan, Shanshan Qin, Wen Li, Weibin Wu, Jian Yang, Maoping Chu, Xiaokun Li, Yuqing Huo, Gary L Schaer, Shenming Wang and 1 more

Open access · greenAbstract read
In one paragraph

Article in Journal of the American College of Cardiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed, 1 pooled it
4.2field-weighted citation impact, top 5% 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

68 citing papers in PubMed, 1 synthesis or guideline pooled it, 125 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Review
  6. Review
  7. Observational
  8. Review
  9. The effect of miR-223-3p on endothelial cells in coronary artery disease.In vitro cellular & developmental biology. Animal · 2024
    Article
  10. Review
  11. Review
  12. Circulating and Cardiac Tissue miRNAs in Children with Dilated Cardiomyopathy.Journal of cardiovascular development and disease · 2023
    Article
  13. Article
  14. Review
  15. Platelet-Derived Extracellular Vesicles in Arterial Thrombosis.Advances in experimental medicine and biology · 2023
    Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Review

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 4 institutions in 2 countries.

Zhen ShanRush University Cardiovascular Research Center and Department of Pharmacology, Rush University Medical Center, Chicago, Illinois.
Shanshan QinRush University Cardiovascular Research Center and Department of Pharmacology, Rush University Medical Center, Chicago, Illinois.
Wen LiDivision of Vascular Surgery and the Laboratory of General Surgery, First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Weibin WuDivision of Vascular Surgery and the Laboratory of General Surgery, First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Jian YangRush University Cardiovascular Research Center and Department of Pharmacology, Rush University Medical Center, Chicago, Illinois.
Maoping ChuWenzhou Medical University, Second Affiliated Hospital, Wenzhou, China.
Xiaokun LiWenzhou Medical University, Second Affiliated Hospital, Wenzhou, China.
Yuqing HuoVascular Biology Center, Medical College of Georgia, Georgia Health Sciences University, Augusta, Georgia.
Gary L SchaerRush University Cardiovascular Research Center and Department of Pharmacology, Rush University Medical Center, Chicago, Illinois.
Shenming WangDivision of Vascular Surgery and the Laboratory of General Surgery, First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China. Electronic address: shenmingwang@hotmail.com.
Chunxiang ZhangRush University Cardiovascular Research Center and Department of Pharmacology, Rush University Medical Center, Chicago, Illinois. Electronic address: chunxiang_zhang@rush.edu.
Rush University Medical Center · USSun Yat-sen University · CNWenzhou Medical University · CNAugusta University Health · US

Funding

Role of miR-145 in Vascular Smooth Muscle Cell BiologyRole ofR01HL095707 · NHLBI · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI ZHANG, CHUNXIANG · 2010 to 2013
$1.5M
The role of adenosine kinase in atherosclerosisR01HL095556 · NHLBI · UNIVERSITY OF MINNESOTA · PI HUO, YUQING · 2011 to 2015
$1.5M
Circulating cell-free microRNAs in atherogenesisR21HL109656 · NHLBI · RUSH UNIVERSITY MEDICAL CENTER · PI ZHANG, CHUNXIANG · 2012 to 2013
$410k
MicroRNA mechanism and therapeutics of impaired wound healingR21NR013876 · NINR · RUSH UNIVERSITY MEDICAL CENTER · PI ZHANG, CHUNXIANG · 2012 to 2013
$409k
NHLBI NIH HHS HL095707NHLBI NIH HHS HL109656NHLBI NIH HHS R01 HL095556NHLBI NIH HHS R01 HL095707NHLBI NIH HHS R21 HL109656NINR NIH HHS NR013876NINR NIH HHS R21 NR013876
6 · The paper itself

Abstract

backgroundMicroRNA-223 (miR-223) is a hematopoietic lineage cell-specific microRNA. However, a significant amount of miR-223 has been identified in vascular smooth muscle cells (VSMCs) and vascular walls that should not have endogenous miR-223.

objectivesThis study sought to determine the sources of miR-223 in normal and atherosclerotic arteries and the role of miR-223 in atherogenesis.

methodsThe levels and sources of miR-223 in blood cells (leukocytes and platelets), serum, blood microparticles, VSMCs, and vascular walls were determined. Both in vivo and in vitro studies were conducted to evaluate miR-223 secretion by blood cells and the ability of miR-223 to enter VSMCs and vascular walls. Subsequent changes in and the effects of miR-223 levels on serum and arteries in atherosclerotic animals and patients were investigated.

resultsBlood cells were able to secrete miR-223 into serum. MicroRNA-223 from blood cells was the most abundant cell-free miRNA in blood. Blood cell-secreted miR-223 could enter VSMCs and vascular walls, which produced strong biological effects via its target genes. In both atherosclerotic apolipoprotein-E knockout mice and patients with atherosclerosis, miR-223 levels were significantly increased in serum and atherosclerotic vascular walls. The atherosclerotic lesions in apolipoprotein-E knockout mice were exacerbated by miR-223 knockdown. The effect of miR-223 on atherogenesis was verified using miR-223 knockout mice.

conclusionsBlood cell-secreted miR-223 enters vascular cells and walls, and appears to play important roles in VSMC function and atherogenesis. As a novel endocrine genetic signal between blood cells and vascular cells, miR-223 may provide a novel mechanism and new therapeutic target for atherosclerosis.

Indexed as

AnimalsAtherosclerosisBlood CellsCells, CulturedMaleMiceMice, Inbred C57BLMice, KnockoutMicroRNAsMuscle, Smooth, VascularMyocytes, Smooth MuscleRatsRats, Sprague-DawleyMicroRNAsMIRN223 microRNA, mouseatherosclerosisbone marrowinsulin-like growth factor 1 receptormicroRNAs

Identifiers

PMID26065992
PMCPMC4498487
OpenAlexW624690144

What OpenQuestion holds

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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.