Evidence map›Paper›PMID 25848249›Full record

ArticleInternational journal of nanomedicine2015

Silica nanoparticles increase human adipose tissue-derived stem cell proliferation through ERK1/2 activation.

Ki Joo Kim, Young Ae Joe, Min Kyoung Kim, Su Jin Lee, Yeon Hee Ryu, Dong-Woo Cho, Jong Won Rhie

Open access · goldAbstract read
In one paragraph

Article in International journal of nanomedicine, 2015. 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
4.5field-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

25 citing papers in PubMed, 64 citations in OpenAlex.

  1. Review
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  4. Silica-Based Advanced Nanoparticles For Treating Ischemic Disease.Tissue engineering and regenerative medicine · 2023
    Review
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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

7 authors at 3 institutions in 2 countries.

Ki Joo KimDepartment of Plastic Surgery, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea ; Department of Molecular Biomedicine, The Catholic University of Korea, Seoul, Republic of Korea.
Young Ae JoeCancer Research Institute and Department of Medical Lifescience, The Catholic University of Korea, Seoul, Republic of Korea.
Min Kyoung KimDepartment of Plastic Surgery, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea ; Department of Molecular Biomedicine, The Catholic University of Korea, Seoul, Republic of Korea.
Su Jin LeeDepartment of Plastic Surgery, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Yeon Hee RyuDepartment of Plastic Surgery, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea ; Department of Molecular Biomedicine, The Catholic University of Korea, Seoul, Republic of Korea.
Dong-Woo ChoDepartment of Mechanical Engineering, Pohang University of Science and Technology, Gyeongbuk, Republic of Korea ; Department of Integrative Bioscience and Bioengineering, Pohang University of Science and Technology, Gyeongbuk, Republic of Korea.
Jong Won RhieDepartment of Plastic Surgery, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea ; Department of Molecular Biomedicine, The Catholic University of Korea, Seoul, Republic of Korea.
Max Planck Institute for Molecular Biomedicine · DECatholic University of Korea · KRPohang University of Science and Technology · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSilicon dioxide composites have been found to enhance the mechanical properties of scaffolds and to support growth of human adipose tissue-derived stem cells (hADSCs) both in vitro and in vivo. Silica (silicon dioxide alone) exists as differently sized particles when suspended in culture medium, but it is not clear whether particle size influences the beneficial effect of silicon dioxide on hADSCs. In this study, we examined the effect of different sized particles on growth and mitogen-activated protein kinase signaling in hADSCs.

methodsSilica gel was prepared by a chemical reaction using hydrochloric acid and sodium silicate, washed, sterilized, and suspended in serum-free culture medium for 48 hours, and then sequentially filtered through a 0.22 μm filter (filtrate containing nanoparticles smaller than 220 nm; silica NPs). hADSCs were incubated with silica NPs or 3 μm silica microparticles (MPs), examined by transmission electron microscopy, and assayed for cell proliferation, apoptosis, and mitogen-activated protein kinase signaling.

resultsEighty-nine percent of the silica NPs were around 50-120 nm in size. When hADSCs were treated with the study particles, silica NPs were observed in endocytosed vacuoles in the cytosol of hADSCs, but silica MPs showed no cell entry. Silica NPs increased the proliferation of hADSCs, but silica MPs had no significant effect in this regard. Instead, silica MPs induced slight apoptosis. Silica NPs increased phosphorylation of extracellular signal-related kinase (ERK)1/2, while silica MPs increased phosphorylation of p38. Silica NPs had no effect on phosphorylation of Janus kinase or p38. Pretreatment with PD98059, a MEK inhibitor, prevented the ERK1/2 phosphorylation and proliferation induced by silica NPs.

conclusionScaffolds containing silicon dioxide for tissue engineering may enhance cell growth through ERK1/2 activation only when NPs around 50-120 nm in size are included, and single component silica-derived NPs could be useful for bioscaffolds in stem cell therapy.

Indexed as

NanoparticlesAdipose TissueApoptosisCell ProliferationCells, CulturedFlavonoidsHumansMAP Kinase Signaling SystemMicroscopy, Electron, TransmissionMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3Particle SizePhosphorylationSignal TransductionSilicon DioxideStem Cells2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-oneFlavonoidsMAPK1 protein, humanMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3Silicon DioxidebiomaterialceramicERKmesenchymal stem cellsparticle

Identifiers

PMID25848249
PMCPMC4378289
OpenAlexW2015537367

What OpenQuestion holds

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LicenceCC BY-NC
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.