How Reversible Are the Effects of Fumed Silica on Macrophages? A Proteomics-Informed View

Synthetic amorphous silica is one of the most used nanomaterials, and numerous toxicological studies have studied its effects. Most of these studies have used an acute exposure mode to investigate the effects immediately after exposure. However, this exposure modality does not allow the investigation of the persistence of the effects, which is a crucial aspect of silica toxicology, as exemplified by crystalline silica. In this paper, we extended the investigations by studying not only the responses immediately after exposure but also after a 72 h post-exposure recovery phase. We used a pyrolytic silica as the test nanomaterial, as this variant of synthetic amorphous silica has been shown to induce a more persistent inflammation in vivo than precipitated silica. To investigate macrophage responses to pyrolytic silica, we used a combination of proteomics and targeted experiments, which allowed us to show that most of the cellular functions that were altered immediately after exposure to pyrolytic silica at a subtoxic dose, such as energy metabolism and cell morphology, returned to normal at the end of the recovery period. However, some alterations, such as the inflammatory responses and some aldehyde detoxification proteins, were persistent. At the proteomic level, other alterations, such as proteins implicated in the endosomal/lysosomal pathway, were also persistent but resulted in normal function, thus suggesting cellular adaptation.

[1]  S. Cianférani,et al.  The longer the worse: a combined proteomic and targeted study of the long-termversusshort-term effects of silver nanoparticles on macrophages , 2020 .

[2]  T. Rabilloud,et al.  Repeated vs. Acute Exposure of RAW264.7 Mouse Macrophages to Silica Nanoparticles: A Bioaccumulation and Functional Change Study , 2020, Nanomaterials.

[3]  S. Ravanel,et al.  How reversible are the effects of silver nanoparticles on macrophages? A proteomic-instructed view , 2019, Environmental Science: Nano.

[4]  T. Rabilloud,et al.  A toxicology-informed, safer by design approach for the fabrication of transparent electrodes based on silver nanowires , 2019, Environmental Science: Nano.

[5]  M. Berchtold,et al.  ALG-2 participates in recovery of cells after plasma membrane damage by electroporation and digitonin treatment , 2018, PloS one.

[6]  Y. Liu,et al.  An autophagy assay reveals the ESCRT-III component CHMP2A as a regulator of phagophore closure , 2018, Nature Communications.

[7]  C. Bain,et al.  Barrier-tissue macrophages: functional adaptation to environmental challenges , 2017, Nature Medicine.

[8]  G. Schoehn,et al.  Differential proteomics highlights macrophage-specific responses to amorphous silica nanoparticles. , 2017, Nanoscale.

[9]  E. Filippi-Chiela,et al.  Ratiometric analysis of Acridine Orange staining in the study of acidic organelles and autophagy , 2016, Journal of Cell Science.

[10]  C. Brinker,et al.  Repetitive Dosing of Fumed Silica Leads to Profibrogenic Effects through Unique Structure-Activity Relationships and Biopersistence in the Lung. , 2016, ACS nano.

[11]  N. Herlin‐Boime,et al.  Different in vitro exposure regimens of murine primary macrophages to silver nanoparticles induce different fates of nanoparticles and different toxicological and functional consequences , 2016, Nanotoxicology.

[12]  A. P. Bell,et al.  Proinflammatory Effects of Pyrogenic and Precipitated Amorphous Silica Nanoparticles in Innate Immunity Cells. , 2016, Toxicological sciences : an official journal of the Society of Toxicology.

[13]  J. Ravanat,et al.  A combined proteomic and targeted analysis unravels new toxic mechanisms for zinc oxide nanoparticles in macrophages. , 2016, Journal of proteomics.

[14]  D. Lison,et al.  Revisiting the paradigm of silica pathogenicity with synthetic quartz crystals: the role of crystallinity and surface disorder , 2015, Particle and Fibre Toxicology.

[15]  A. van Dorsselaer,et al.  Comparative Proteomic Analysis of the Molecular Responses of Mouse Macrophages to Titanium Dioxide and Copper Oxide Nanoparticles Unravels Some Toxic Mechanisms for Copper Oxide Nanoparticles in Macrophages , 2015, PloS one.

[16]  J. Sallenave,et al.  Acute exposure to silica nanoparticles enhances mortality and increases lung permeability in a mouse model of Pseudomonas aeruginosa pneumonia , 2015, Particle and Fibre Toxicology.

[17]  C. Vulpe,et al.  Short versus long silver nanowires: a comparison of in vivo pulmonary effects post instillation , 2014, Particle and Fibre Toxicology.

[18]  T. Homma,et al.  Reductive detoxification of acrolein as a potential role for aldehyde reductase (AKR1A) in mammals. , 2014, Biochemical and biophysical research communications.

[19]  James C. Kirkpatrick,et al.  The protein corona protects against size- and dose-dependent toxicity of amorphous silica nanoparticles , 2014, Beilstein journal of nanotechnology.

[20]  Alan R. Boobis,et al.  Elucidation of Toxicity Pathways in Lung Epithelial Cells Induced by Silicon Dioxide Nanoparticles , 2013, PloS one.

[21]  Joel G. Pounds,et al.  Dysregulation of macrophage activation profiles by engineered nanoparticles. , 2013, ACS nano.

[22]  S. Retterer,et al.  Dynamic development of the protein corona on silica nanoparticles: composition and role in toxicity. , 2013, Nanoscale.

[23]  Tian Xia,et al.  Processing pathway dependence of amorphous silica nanoparticle toxicity: colloidal vs pyrolytic. , 2012, Journal of the American Chemical Society.

[24]  G. Mazzucco,et al.  Physicochemical determinants in the cellular responses to nanostructured amorphous silicas. , 2012, Toxicological sciences : an official journal of the Society of Toxicology.

[25]  Richard C Zangar,et al.  Cellular recognition and trafficking of amorphous silica nanoparticles by macrophage scavenger receptor A , 2011, Nanotoxicology.

[26]  Yi Shen,et al.  Human aldo-keto reductases 1B1 and 1B10: a comparative study on their enzyme activity toward electrophilic carbonyl compounds. , 2011, Chemico-biological interactions.

[27]  M. Poidevin,et al.  Inner‐membrane proteins PMI/TMEM11 regulate mitochondrial morphogenesis independently of the DRP1/MFN fission/fusion pathways , 2011, EMBO reports.

[28]  P. Boya,et al.  Tumor suppressor p27Kip1 undergoes endolysosomal degradation through its interaction with sorting nexin 6 , 2010, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[29]  Mara Ghiazza,et al.  Does vitreous silica contradict the toxicity of the crystalline silica paradigm? , 2010, Chemical research in toxicology.

[30]  Håkan Wallin,et al.  Protracted elimination of gold nanoparticles from mouse liver. , 2009, Nanomedicine : nanotechnology, biology, and medicine.

[31]  S. Gygi,et al.  An FTS/Hook/p107(FHIP) complex interacts with and promotes endosomal clustering by the homotypic vacuolar protein sorting complex. , 2008, Molecular biology of the cell.

[32]  R. Hamilton,et al.  Silica binding and toxicity in alveolar macrophages. , 2008, Free radical biology & medicine.

[33]  J. Arts,et al.  Five-day inhalation toxicity study of three types of synthetic amorphous silicas in Wistar rats and post-exposure evaluations for up to 3 months. , 2007, Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association.

[34]  David B Warheit,et al.  Assessing toxicity of fine and nanoparticles: comparing in vitro measurements to in vivo pulmonary toxicity profiles. , 2007, Toxicological sciences : an official journal of the Society of Toxicology.

[35]  H. Krämer,et al.  The Microtubule-binding Protein Hook3 Interacts with a Cytoplasmic Domain of Scavenger Receptor A* , 2007, Journal of Biological Chemistry.

[36]  E. Krieger,et al.  The human Vps29 retromer component is a metallo-phosphoesterase for a cation-independent mannose 6-phosphate receptor substrate peptide. , 2006, The Biochemical journal.

[37]  A. Hamvas,et al.  Surfactant Composition and Function in Patients with ABCA3 Mutations , 2006, Pediatric Research.

[38]  C. Giardina,et al.  Silica-induced apoptosis in mouse alveolar macrophages is initiated by lysosomal enzyme activity. , 2004, Toxicological sciences : an official journal of the Society of Toxicology.

[39]  D. V. Vander Jagt,et al.  Metabolism of the 2-oxoaldehyde methylglyoxal by aldose reductase and by glyoxalase-I: roles for glutathione in both enzymes and implications for diabetic complications. , 2001, Chemico-biological interactions.

[40]  G. Rastelli,et al.  Aldose reductase does catalyse the reduction of glyceraldehyde through a stoichiometric oxidation of NADPH. , 2000, Experimental eye research.

[41]  C Hermans,et al.  Human bronchoalveolar lavage fluid protein two‐dimensional database: Study of interstitial lung diseases , 2000, Electrophoresis.

[42]  D. Harrison,et al.  Major differences exist in the function and tissue-specific expression of human aflatoxin B1 aldehyde reductase and the principal human aldo-keto reductase AKR1 family members. , 1999, The Biochemical journal.

[43]  S. Bottomley,et al.  The intracellular serpin proteinase inhibitor 6 is expressed in monocytes and granulocytes and is a potent inhibitor of the azurophilic granule protease, cathepsin G. , 1999, Blood.

[44]  R. Iyer,et al.  Silica-induced apoptosis mediated via scavenger receptor in human alveolar macrophages. , 1996, Toxicology and applied pharmacology.

[45]  M. Maines,et al.  Detection of 10 variants of biliverdin reductase in rat liver by two-dimensional gel electrophoresis. , 1989, The Journal of biological chemistry.

[46]  F. Kwok,et al.  Brain pyridoxal kinase. Purification and characterization. , 1986, European journal of biochemistry.

[47]  Liping Tang,et al.  A simple method to visualize and assess the integrity of lysosomal membrane in mammalian cells using a fluorescent dye. , 2013, Methods in molecular biology.

[48]  T. Langer,et al.  Prohibitin function within mitochondria: essential roles for cell proliferation and cristae morphogenesis. , 2009, Biochimica et biophysica acta.

[49]  R. Wattiez,et al.  Sample preparation of bronchoalveolar lavage fluid. , 2008, Methods in molecular biology.

[50]  Brad T. Sherman,et al.  Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources , 2008, Nature Protocols.

[51]  W. Krietsch,et al.  [18] Phosphoglycerate kinase from animal tissue , 1982 .

[52]  G. Valentini,et al.  AMP- and fructose 1,6-bisphosphate-activated pyruvate kinases from Escherichia coli. , 1982, Methods in enzymology.

[53]  W. Krietsch,et al.  Phosphoglycerate kinase from animal tissue. , 1982, Methods in enzymology.