Evidence map›Paper›PMID 24743945›Full record

ArticlePloS one2014

MiR-142-3p attenuates the migration of CD4⁺ T cells through regulating actin cytoskeleton via RAC1 and ROCK2 in arteriosclerosis obliterans.

Jiawei Liu, Wen Li, Siwen Wang, Yidan Wu, Zilun Li, Wenjian Wang, Ruiming Liu, Jingsong Ou, Chunxiang Zhang, Shenming Wang

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

25 citing papers in PubMed, 44 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. MicroRNA profile of circulating CD4BMC cardiovascular disorders · 2022
    Article
  5. Rho Kinases in Embryonic Development and Stem Cell Research.Archivum immunologiae et therapiae experimentalis · 2022
    Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. Artesunate promotes Th1 differentiation from CD4+ T cells to enhance cell apoptosis in ovarian cancer via miR-142.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2019
    Article
  18. Article
  19. 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

10 authors at 2 institutions in 2 countries.

Jiawei LiuDepartment of Vascular Surgery, the First Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong, China.
Wen LiLaboratory of General Surgery, the First Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong, China.
Siwen WangDepartment of Vascular Surgery, the First Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong, China.
Yidan WuDepartment of Vascular Surgery, the First Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong, China.
Zilun LiDepartment of Vascular Surgery, the First Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong, China.
Wenjian WangDepartment of Vascular Surgery, the First Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong, China.
Ruiming LiuDepartment of Vascular Surgery, the First Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong, China.
Jingsong OuDepartment of Vascular Surgery, the First Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong, China.
Chunxiang ZhangCardiovascular Research Center, Department of Pharmacology, Rush Medical College, Rush University, Chicago, Illinois, United States of America.
Shenming WangDepartment of Vascular Surgery, the First Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong, China.
Sun Yat-sen University · CNRush University Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The migration of CD4+ T cells plays an important role in arteriosclerosis obliterans (ASO). However, the molecular mechanisms involved in CD4+ T cell migration are still unclear. The current study is aimed to determine the expression change of miR-142-3p in CD4+ T cells from patients with ASO and investigate its role in CD4+ T cell migration as well the potential mechanisms involved. We identified by qRT-PCR and in situ hybridization that the expression of miR-142-3p in CD4+ T cells was significantly down-regulated in patients with ASO. Chemokine (C-X-C motif) ligand 12 (CXCL12), a common inflammatory chemokine under the ASO condition, was able to down-regulate the expression of miR-142-3p in cultured CD4+ T cells. Up-regulation of miR-142-3p by lentivirus-mediated gene transfer had a strong inhibitory effect on CD4+ T cell migration both in cultured human cells in vitro and in mouse aortas and spleens in vivo. RAC1 and ROCK2 were identified to be the direct target genes in human CD4+ T cells, which are further confirmed by dual luciferase assay. MiR-142-3p had strong regulatory effects on actin cytoskeleton as shown by the actin staining in CD4+ T cells. The results suggest that the expression of miR-142-3p is down-regulated in CD4+ T cells from patients with ASO. The down-regulation of miR-142-3p could increase the migration of CD4+ T cells to the vascular walls by regulation of actin cytoskeleton via its target genes, RAC1 and ROCK2.

Indexed as

Actin CytoskeletonAgedAnimalsArteriosclerosis ObliteransCD4-Positive T-LymphocytesCell MovementCells, CulturedFemaleHumansIn Situ HybridizationMaleMiceMicroRNAsrac1 GTP-Binding Proteinrho-Associated KinasesMicroRNAsMIRN142 microRNA, humanrac1 GTP-Binding ProteinRAC1 protein, humanrho-Associated KinasesROCK2 protein, human

Identifiers

PMID24743945
PMCPMC3990671
OpenAlexW2048860926

What OpenQuestion holds

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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.