Evidence map›Paper›PMID 28796831›Full record

ArticlePloS one2017

The species origin of the serum in the culture medium influences the in vitro toxicity of silica nanoparticles to HepG2 cells.

Cédric Pisani, Estelle Rascol, Christophe Dorandeu, Jean-Charles Gaillard, Clarence Charnay, Yannick Guari, Joël Chopineau, Jean Armengaud, Jean-Marie Devoisselle, Odette Prat

Abstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–field-weighted citation impact
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

16 citing papers in PubMed.

  1. Article
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  10. Review
  11. Machine learning predicts the functional composition of the protein corona and the cellular recognition of nanoparticles.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  12. Review
  13. 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.

Cédric PisaniInstitut Charles Gerhardt de Montpellier, MACS, UMR 5253 CNRS-ENSCM-UM, Place Eugène Bataillon, Montpellier, France.
Estelle RascolInstitut Charles Gerhardt de Montpellier, MACS, UMR 5253 CNRS-ENSCM-UM, Place Eugène Bataillon, Montpellier, France.
Christophe DorandeuInstitut Charles Gerhardt de Montpellier, MACS, UMR 5253 CNRS-ENSCM-UM, Place Eugène Bataillon, Montpellier, France.
Jean-Charles GaillardCEA, Direction de la Recherche Fondamentale-IBITECS, Site de Marcoule, Bagnols-sur-Cèze, France.
Clarence CharnayInstitut Charles Gerhardt de Montpellier, IMNO, UMR 5253 CNRS-ENSCM-UM, 1701, Place Eugène Bataillon, Montpellier, France.
Yannick GuariInstitut Charles Gerhardt de Montpellier, IMNO, UMR 5253 CNRS-ENSCM-UM, 1701, Place Eugène Bataillon, Montpellier, France.
Joël ChopineauInstitut Charles Gerhardt de Montpellier, MACS, UMR 5253 CNRS-ENSCM-UM, Place Eugène Bataillon, Montpellier, France.
Jean ArmengaudCEA, Direction de la Recherche Fondamentale-IBITECS, Site de Marcoule, Bagnols-sur-Cèze, France.
Jean-Marie DevoisselleInstitut Charles Gerhardt de Montpellier, MACS, UMR 5253 CNRS-ENSCM-UM, Place Eugène Bataillon, Montpellier, France.
Odette PratCEA, Direction de la Recherche Fondamentale-BIAM, Site de Marcoule, Bagnols-sur-Cèze, France.ORCID http://orcid.org/0000-0002-8710-3525

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The formation of a protein corona around nanoparticles can influence their toxicity, triggering cellular responses that may be totally different from those elicited by pristine nanoparticles. The main objective of this study was to investigate whether the species origin of the serum proteins forming the corona influences the in vitro toxicity assessment of silica nanoparticles. Coronas were preformed around nanoparticles before cell exposures by incubation in fetal bovine (FBS) or human (HS) serum. The compositions of these protein coronas were assessed by nano-LC MS/MS. The effects of these protein-coated nanoparticles on HepG2 cells were monitored using real-time cell impedance technology. The nanoparticle coronas formed in human or fetal bovine serum comprised many homologous proteins. Using human compared with fetal bovine serum, nanoparticle toxicity in HepG2 cells decreased by 4-fold and 1.5-fold, when used at 50 and 10μg/mL, respectively. It is likely that "markers of self" are present in the serum and are recognized by human cell receptors. Preforming a corona with human serum seems to be more appropriate for in vitro toxicity testing of potential nanocarriers using human cells. In vitro cytotoxicity assays must reflect in vivo conditions as closely as possible to provide solid and useful results.

Indexed as

Metal NanoparticlesSilicon DioxideAnimalsBlood ProteinsCattleCulture MediaHep G2 CellsHumansSpecies SpecificityTandem Mass SpectrometryBlood ProteinsCulture MediaSilicon Dioxide

Identifiers

PMID28796831
PMCPMC5552166

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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.