Evidence map›Paper›PMID 32770080›Full record

ArticleExperimental & molecular medicine2020

NF-κB-dependent miR-31/155 biogenesis is essential for TNF-α-induced impairment of endothelial progenitor cell function.

Ji-Hee Kim, Ji-Yoon Kim, Minsik Park, Suji Kim, Taesam Kim, Joohwan Kim, Seunghwan Choi, Wonjin Park, Jong Yun Hwang, Jongseon Choe and 5 more

Open access · goldAbstract read
In one paragraph

Article in Experimental & molecular medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
0.8field-weighted citation impact, top 22% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 16 citations in OpenAlex.

  1. Changes in microRNA expression associated with preeclampsia: a systematic review.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2025
    Pooled it
  2. Article
  3. Article
  4. The pharmaco-epigenetics of hypertension: a focus on microRNA.Molecular and cellular biochemistry · 2024
    Review
  5. Review
  6. Article
  7. Endothelial progenitor cells in pregnancy-related diseases.Clinical science (London, England : 1979) · 2023
    Review
  8. Article
  9. TrimethylamineInternational journal of molecular sciences · 2021
    Article
  10. Review
  11. Regulation of Osteoclastogenesis and Bone Resorption by miRNAs.Frontiers in cell and developmental biology · 2021
    Review
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

15 authors at 2 institutions in 1 country.

Ji-Hee Kim *Department of Molecular and Cellular Biochemistry, Kangwon National University School of Medicine, Chuncheon, Gangwon-do, 24341, South Korea.
Ji-Yoon Kim *Department of Anesthesiology and Pain Medicine, Hanyang University Hospital, Seoul, 04763, South Korea.
Minsik ParkDepartment of Molecular and Cellular Biochemistry, Kangwon National University School of Medicine, Chuncheon, Gangwon-do, 24341, South Korea.
Suji KimDepartment of Molecular and Cellular Biochemistry, Kangwon National University School of Medicine, Chuncheon, Gangwon-do, 24341, South Korea.
Taesam KimDepartment of Molecular and Cellular Biochemistry, Kangwon National University School of Medicine, Chuncheon, Gangwon-do, 24341, South Korea.
Joohwan KimDepartment of Molecular and Cellular Biochemistry, Kangwon National University School of Medicine, Chuncheon, Gangwon-do, 24341, South Korea.
Seunghwan ChoiDepartment of Molecular and Cellular Biochemistry, Kangwon National University School of Medicine, Chuncheon, Gangwon-do, 24341, South Korea.
Wonjin ParkDepartment of Molecular and Cellular Biochemistry, Kangwon National University School of Medicine, Chuncheon, Gangwon-do, 24341, South Korea.
Jong Yun HwangDepartment of Obstetrics and Gynecology, Kangwon National University School of Medicine, Chuncheon, Gangwon-do, 24341, South Korea.
Jongseon ChoeDepartment of Immunology, Kangwon National University School of Medicine, Chuncheon, Gangwon-do, 24341, South Korea.
Kwon-Soo HaDepartment of Molecular and Cellular Biochemistry, Kangwon National University School of Medicine, Chuncheon, Gangwon-do, 24341, South Korea.ORCID http://orcid.org/0000-0002-4219-1787
Moo-Ho WonDepartment of Neurobiology, Kangwon National University School of Medicine, Chuncheon, Gangwon-do, 24341, South Korea.ORCID http://orcid.org/0000-0002-2038-2160
Sungwoo RyooDepartment of Life Sciences, College of Natural Sciences, Kangwon National University, Chuncheon, Gangwon-do, South Korea.
Young-Guen KwonDepartment of Biochemistry, College of Life Science and Biotechnology, Yonsei University, Seoul, 03722, South Korea.
Young-Myeong KimDepartment of Molecular and Cellular Biochemistry, Kangwon National University School of Medicine, Chuncheon, Gangwon-do, 24341, South Korea. ymkim@kangwon.ac.kr.
Kangwon National University · KRYonsei University · KR

Funding

National Research Foundation of Korea (NRF) 2016M3A9B6903103National Research Foundation of Korea (NRF) 2017R1A2B3004565
6 · The paper itself

Abstract

Endothelial progenitor cell (EPC) dysfunction impairs vascular function and remodeling in inflammation-associated diseases, including preeclampsia. However, the underlying mechanism of this inflammation-induced dysfunction remains unclear. In the present study, we found increases in TNF-α and miR-31/155 levels and reduced numbers of circulating EPCs in patients with preeclampsia. Patient-derived mononuclear cells (MNCs) cultured in autologous serum had decreased endothelial nitric oxide synthase (eNOS) expression, nitric oxide production, and differentiation into EPCs with angiogenic potential, and these effects were inhibited by a TNF-α-neutralizing antibody and miR-31/155 inhibitors. Moreover, TNF-α treatment of normal MNCs increased miR-31/155 biogenesis, decreased eNOS expression, reduced EPC differentiation, and impaired angiogenic potential. The TNF-α-induced impairment of EPC differentiation and function was rescued by NF-κB p65 knockdown or miR-31/155 inhibitors. In addition, treatment of MNCs with synthetic miR-31/155 or an eNOS inhibitor mimicked the inhibitory effects of TNF-α on eNOS expression and EPC functions. Moreover, transplantation of EPCs that had been differentiated from TNF-α-treated MNCs decreased neovascularization and blood perfusion in ischemic mouse hindlimbs compared with those of normally differentiated EPCs. These findings suggest that NF-κB activation is required for TNF-α-induced impairment of EPC mobilization, differentiation, and function via miR-31/155 biogenesis and eNOS downregulation. Our data provide a new role for NF-κB-dependent miR-31/155 in EPC dysfunction under the pathogenic conditions of inflammation-associated vascular diseases, including preeclampsia.

Indexed as

AnimalsCell DifferentiationDown-RegulationEndothelial Progenitor CellsFemaleHindlimbHumansIschemiaMaleMice, NudeMicroRNAsNeovascularization, PhysiologicNF-kappa BNitric Oxide Synthase Type IIIPre-EclampsiaPregnancyMicroRNAsMIRN155 microRNA, humanMIRN31 microRNA, humanNF-kappa BNitric Oxide Synthase Type IIITumor Necrosis Factor-alpha

Identifiers

PMID32770080
PMCPMC8080610
OpenAlexW3047654961

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.