Evidence map›Paper›PMID 26402437›Full record

ArticleJournal of biomedical materials research. Part A2016

Biphasic responses of human vascular smooth muscle cells to magnesium ion.

Jun Ma, Nan Zhao, Donghui Zhu

Open access · greenAbstract read
In one paragraph

Article in Journal of biomedical materials research. Part A, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
4.1field-weighted citation impact, top 6% 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

27 citing papers in PubMed, 80 citations in OpenAlex.

  1. Article
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  6. Micro-Gel Ensembles for Accelerated Healing of Chronic Wound via pH Regulation.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2022
    Article
  7. Leptin and its relationship with magnesium biomarkers in women with obesity.Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine · 2022
    Article
  8. Review
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  15. Review
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  18. Magnesium Regulates Endothelial Barrier Functions through TRPM7, MagT1, and S1P1.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2019
    Article
  19. Article
  20. 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

3 authors at 1 institution in 1 country.

Jun MaDepartment of Chemical, Biological and Bio-Engineering, North Carolina Agricultural and Technical State University, Greensboro, North Carolina, 27411.
Nan ZhaoDepartment of Chemical, Biological and Bio-Engineering, North Carolina Agricultural and Technical State University, Greensboro, North Carolina, 27411.
Donghui ZhuDepartment of Chemical, Biological and Bio-Engineering, North Carolina Agricultural and Technical State University, Greensboro, North Carolina, 27411.
North Carolina Agricultural and Technical State University · US

Funding

Magnesium and alloying elements on vascular cells healthSC3GM113762 · NIGMS · NORTH CAROLINA AGRI & TECH ST UNIV · PI ZHU, DONGHUI · 2015 to 2016
$108k
NIGMS NIH HHS SC3 GM113762NIGMS NIH HHS SC3GM113762
6 · The paper itself

Abstract

Magnesium-based alloys are promising in biodegradable cardiovascular stent applications. The degradation products of magnesium stents may have significant impacts on the surrounding vascular cells. However, knowledge on the interactions between magnesium ion and vascular cells at the molecular and cellular levels is still largely missing. Vascular smooth muscle cell (SMC) plays an important role in the pathogenesis of restenosis and wound healing after stent implantation. This study evaluated the short-term effects of extracellular magnesium ion (Mg(2+)) on the cellular behaviors of SMCs. Cellular responses to Mg(2+) were biphasic and in a concentration-dependent manner. Low concentrations (10 mM) of Mg(2+) increased cell viability, cell proliferation rate, cell adhesion, cell spreading, cell migration rate, and actin expression. In contrast, higher concentrations (40-60 mM) of Mg(2+) had deleterious effects on cells. Gene expression analysis revealed that Mg(2+) altered the expressions of genes mostly related to cell adhesion, cell injury, angiogenesis, inflammation, coagulation, and cell growth. Finding from this study provides some valuable information on SMC responses toward magnesium ions at the cellular and molecular levels, and guidance for future controlled release of magnesium from the stent material.

Indexed as

Cell AdhesionCell MovementCell ProliferationCell SurvivalDose-Response Relationship, DrugGene Expression RegulationHumansMagnesiumMuscle, Smooth, VascularMyocytes, Smooth MuscleMagnesiumcardiovascular stentcell migrationcell morphologymagnesium ionsmooth muscle cell

Identifiers

PMID26402437
PMCPMC4873954
OpenAlexW2126058729

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.