Evidence map›Paper›PMID 25326241›Full record

ArticleToxicological sciences : an official journal of the Society of Toxicology2015

Formation of a protein corona on silver nanoparticles mediates cellular toxicity via scavenger receptors.

Jonathan H Shannahan, Ramakrishna Podila, Abdullah A Aldossari, Hilary Emerson, Brian A Powell, Pu Chun Ke, Apparao M Rao, Jared M Brown

Open access · bronzeAbstract read
In one paragraph

Article in Toxicological sciences : an official journal of the Society of Toxicology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 74 papers.

0numbers the graph read from it
0cells of the map it votes in
74citing papers in PubMed
7.3field-weighted citation impact, top 2% 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

74 citing papers in PubMed, 157 citations in OpenAlex.

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14 more citing papers are in PubMed but not listed here.

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

8 authors at 1 institution in 1 country.

Jonathan H Shannahan*Department of Pharmaceutical Sciences, Skaggs School of Pharmacy and Pharmaceutical Sciences, The University of Colorado Anschutz Medical Campus, Aurora, Colorado 80045, Department of Physics and Astronomy, Clemson University, Clemson, South Carolina 29634, Clemson Nanomaterials Center and COMSET, Clemson University, Anderson, South Carolina 29625, and Department of Environmental Engineering and Earth Sciences, Clemson University, Anderson, South Carolina 29625.
Ramakrishna Podila*Department of Pharmaceutical Sciences, Skaggs School of Pharmacy and Pharmaceutical Sciences, The University of Colorado Anschutz Medical Campus, Aurora, Colorado 80045, Department of Physics and Astronomy, Clemson University, Clemson, South Carolina 29634, Clemson Nanomaterials Center and COMSET, Clemson University, Anderson, South Carolina 29625, and Department of Environmental Engineering and Earth Sciences, Clemson University, Anderson, South Carolina 29625 *Department of Pharmaceutical Sciences, Skaggs School of Pharmacy and Pharmaceutical Sciences, The University of Colorado Anschutz Medical Campus, Aurora, Colorado 80045, Department of Physics and Astronomy, Clemson University, Clemson, South Carolina 29634, Clemson Nanomaterials Center and COMSET, Clemson University, Anderson, South Carolina 29625, and Department of Environmental Engineering and Earth Sciences, Clemson University, Anderson, South Carolina 29625.
Abdullah A Aldossari*Department of Pharmaceutical Sciences, Skaggs School of Pharmacy and Pharmaceutical Sciences, The University of Colorado Anschutz Medical Campus, Aurora, Colorado 80045, Department of Physics and Astronomy, Clemson University, Clemson, South Carolina 29634, Clemson Nanomaterials Center and COMSET, Clemson University, Anderson, South Carolina 29625, and Department of Environmental Engineering and Earth Sciences, Clemson University, Anderson, South Carolina 29625.
Hilary Emerson*Department of Pharmaceutical Sciences, Skaggs School of Pharmacy and Pharmaceutical Sciences, The University of Colorado Anschutz Medical Campus, Aurora, Colorado 80045, Department of Physics and Astronomy, Clemson University, Clemson, South Carolina 29634, Clemson Nanomaterials Center and COMSET, Clemson University, Anderson, South Carolina 29625, and Department of Environmental Engineering and Earth Sciences, Clemson University, Anderson, South Carolina 29625.
Brian A Powell*Department of Pharmaceutical Sciences, Skaggs School of Pharmacy and Pharmaceutical Sciences, The University of Colorado Anschutz Medical Campus, Aurora, Colorado 80045, Department of Physics and Astronomy, Clemson University, Clemson, South Carolina 29634, Clemson Nanomaterials Center and COMSET, Clemson University, Anderson, South Carolina 29625, and Department of Environmental Engineering and Earth Sciences, Clemson University, Anderson, South Carolina 29625.
Pu Chun Ke*Department of Pharmaceutical Sciences, Skaggs School of Pharmacy and Pharmaceutical Sciences, The University of Colorado Anschutz Medical Campus, Aurora, Colorado 80045, Department of Physics and Astronomy, Clemson University, Clemson, South Carolina 29634, Clemson Nanomaterials Center and COMSET, Clemson University, Anderson, South Carolina 29625, and Department of Environmental Engineering and Earth Sciences, Clemson University, Anderson, South Carolina 29625.
Apparao M Rao*Department of Pharmaceutical Sciences, Skaggs School of Pharmacy and Pharmaceutical Sciences, The University of Colorado Anschutz Medical Campus, Aurora, Colorado 80045, Department of Physics and Astronomy, Clemson University, Clemson, South Carolina 29634, Clemson Nanomaterials Center and COMSET, Clemson University, Anderson, South Carolina 29625, and Department of Environmental Engineering and Earth Sciences, Clemson University, Anderson, South Carolina 29625 *Department of Pharmaceutical Sciences, Skaggs School of Pharmacy and Pharmaceutical Sciences, The University of Colorado Anschutz Medical Campus, Aurora, Colorado 80045, Department of Physics and Astronomy, Clemson University, Clemson, South Carolina 29634, Clemson Nanomaterials Center and COMSET, Clemson University, Anderson, South Carolina 29625, and Department of Environmental Engineering and Earth Sciences, Clemson University, Anderson, South Carolina 29625.
Jared M Brown*Department of Pharmaceutical Sciences, Skaggs School of Pharmacy and Pharmaceutical Sciences, The University of Colorado Anschutz Medical Campus, Aurora, Colorado 80045, Department of Physics and Astronomy, Clemson University, Clemson, South Carolina 29634, Clemson Nanomaterials Center and COMSET, Clemson University, Anderson, South Carolina 29625, and Department of Environmental Engineering and Earth Sciences, Clemson University, Anderson, South Carolina 29625 jared.brown@ucdenver.edu.
University of Montana · US

Funding

Mechanisms of non-IgE Mast Cell Activation by Environmental ParticulatesR01ES019311 · NIEHS · UNIVERSITY OF COLORADO DENVER · PI BROWN, JARED MICHAEL · 2010 to 2024
$7.0M
Synthesis and Characterization CoreU19ES019525 · NIEHS · RESEARCH TRIANGLE INSTITUTE · PI FENNELL, TIMOTHY RAYMOND · 2010 to 2014
$6.3M
NIEHS NIH HHS R01 ES019311NIEHS NIH HHS U19 ES019525
6 · The paper itself

Abstract

Addition of a protein corona (PC) or protein adsorption layer on the surface of nanomaterials following their introduction into physiological environments may modify their activity, bio-distribution, cellular uptake, clearance, and toxicity. We hypothesize that silver nanoparticles (AgNPs) will associate with proteins common to human serum and cell culture media forming a PC that will impact cell activation and cytotoxicity. Furthermore, the role of scavenger receptor BI (SR-BI) in mediating this toxicity was evaluated. Citrate-suspended 20 nm AgNPs were incubated with human serum albumin (HSA), bovine serum albumin (BSA), high-density lipoprotein (HDL), or water (control) to form a PC. AgNPs associated with each protein (HSA, BSA, and HDL) forming PCs as assessed by electron microscopy, hyperspectral analysis, ζ-potential, and hydrodynamic size. Addition of the PC decreased uptake of AgNPs by rat lung epithelial and rat aortic endothelial cells. Hyperspectral analysis demonstrated a loss of the AgNP PC following internalization. Cells demonstrated concentration-dependent cytotoxicity following exposure to AgNPs with or without PCs (0, 6.25, 12.5, 25 or 50 μg/ml). All PC-coated AgNPs were found to activate cells by inducing IL-6 mRNA expression. A small molecule SR-BI inhibitor was utilized to determine the role of SR-BI in the observed effects. Pretreatment with the SR-BI inhibitor decreased internalization of AgNPs with or without PCs, and reduced both cytotoxicity and IL-6 mRNA expression. This study characterizes the formation of a PC on AgNPs and demonstrates its influence on cytotoxicity and cell activation through a cell surface receptor.

Indexed as

AdsorptionAnimalsAortaCells, CulturedCell SurvivalDose-Response Relationship, DrugEndothelial CellsEpithelial CellsInterleukin-6Lipoproteins, HDLLungMetal NanoparticlesParticle SizeProtein ConformationProtein CoronaRatsALB protein, humanInterleukin-6Lipoproteins, HDLProtein CoronaRNA, MessengerScarb1 protein, ratScavenger Receptors, Class BSerum AlbuminSerum Albumin, BovineSerum Albumin, HumanSilverdarkfield microscopyendothelial cellsepithelial cellshyperspectral microscopyin vitro toxicitynanotoxicology

Identifiers

PMID25326241
PMCPMC4274384
OpenAlexW2078757591

What OpenQuestion holds

Textmetadata
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.