Literature DB >> 30838431

The protein corona suppresses the cytotoxic and pro-inflammatory response in lung epithelial cells and macrophages upon exposure to nanosilica.

Regina Leibe1, I-Lun Hsiao1,2, Susanne Fritsch-Decker1, Ulrike Kielmeier1, Ane Marit Wagbo1, Benjamin Voss1, Annemarie Schmidt1, Sarah Dorothea Hessman1, Albert Duschl3, Gertie Janneke Oostingh4, Silvia Diabaté5, Carsten Weiss6.   

Abstract

Engineered amorphous silica nanoparticles (nanosilica) are one of the most abundant nanomaterials and are widely used in industry. Furthermore, novel nanosilica materials are promising theranostic tools for biomedicine. However, hazardous effects of nanosilica especially after inhalation into the lung have been documented. Therefore, the safe development of nanosilica materials urgently requires predictive assays to monitor toxicity. Here, we further investigate the impact of the protein corona on the biological activity of two different types of nanosilica (colloidal and pyrogenic) in lung cells. As previously described, adsorption of serum proteins to the nanosilica surface suppresses cytotoxicity in macrophages and lung epithelial cells. As the increase of pro-inflammatory mediators is a hallmark of inflammation in the lung upon nanosilica exposure, we studied the potential coupling of the cytotoxic and pro-inflammatory response in A549 human lung epithelial cells and RAW264.7 mouse macrophages. Indeed, cytotoxicity precedes the onset of pro-inflammatory gene expression and cytokine release as exemplified for IL-8 in A549 cells and TNF-alpha in RAW264.7 macrophages after exposure to 0-100 µg/mL nanosilica in medium without serum. Formation of a protein corona not only inhibited cellular toxicity, but also the pro-inflammatory response. Of note, uptake of nanosilica into cells was negligible in the absence, but enhanced in the presence of a protein corona. Hence, the prevailing explanation that the protein corona simply interferes with cellular uptake thus preventing adverse effects needs to be revisited. In conclusion, for the reliable prediction of adverse effects of nanosilica in the lung, in vitro assays should be performed in media not complemented with complete serum. However, in case of different exposure routes, e.g., injection into the blood stream as intended for biomedicine, the protein corona prevents acute toxic actions of nanosilica.

Entities:  

Keywords:  Cell death; Inflammation; Lung cells; Nanoparticle; Nano–bio-interface; Protein corona; Silica

Mesh:

Substances:

Year:  2019        PMID: 30838431     DOI: 10.1007/s00204-019-02422-9

Source DB:  PubMed          Journal:  Arch Toxicol        ISSN: 0340-5761            Impact factor:   5.153


  14 in total

1.  Surface Treatment With Hydrophobic Coating Reagents (Organosilanes) Strongly Reduces the Bioactivity of Synthetic Amorphous Silica in vitro.

Authors:  Martin Wiemann; Antje Vennemann; Tobias B Schuster; Jürgen Nolde; Nils Krueger
Journal:  Front Public Health       Date:  2022-06-21

2.  Comparing α-Quartz-Induced Cytotoxicity and Interleukin-8 Release in Pulmonary Mono- and Co-Cultures Exposed under Submerged and Air-Liquid Interface Conditions.

Authors:  Alexandra Friesen; Susanne Fritsch-Decker; Matthias Hufnagel; Sonja Mülhopt; Dieter Stapf; Andrea Hartwig; Carsten Weiss
Journal:  Int J Mol Sci       Date:  2022-06-08       Impact factor: 6.208

3.  A novel TEM grid sampler for airborne particles to measure the cell culture surface dose.

Authors:  Sonja Mülhopt; Christoph Schlager; Markus Berger; Sivakumar Murugadoss; Peter H Hoet; Tobias Krebs; Hanns-Rudolf Paur; Dieter Stapf
Journal:  Sci Rep       Date:  2020-05-21       Impact factor: 4.379

4.  Cytotoxicity of fractured quartz on THP-1 human macrophages: role of the membranolytic activity of quartz and phagolysosome destabilization.

Authors:  Riccardo Leinardi; Cristina Pavan; Harita Yedavally; Maura Tomatis; Anna Salvati; Francesco Turci
Journal:  Arch Toxicol       Date:  2020-06-26       Impact factor: 5.153

5.  Silica Nanoparticles Provoke Cell Death Independent of p53 and BAX in Human Colon Cancer Cells.

Authors:  Susanne Fritsch-Decker; Zhen An; Jin Yan; Iris Hansjosten; Marco Al-Rawi; Ravindra Peravali; Silvia Diabaté; Carsten Weiss
Journal:  Nanomaterials (Basel)       Date:  2019-08-16       Impact factor: 5.076

6.  p62/SQSTM1 accumulation due to degradation inhibition and transcriptional activation plays a critical role in silica nanoparticle-induced airway inflammation via NF-κB activation.

Authors:  Yifan Wu; Yang Jin; Tianyu Sun; Piaoyu Zhu; Jinlong Li; Qinglin Zhang; Xiaoke Wang; Junkang Jiang; Gang Chen; Xinyuan Zhao
Journal:  J Nanobiotechnology       Date:  2020-05-19       Impact factor: 10.435

Review 7.  A Low-Serum Culture System for Prolonged in Vitro Toxicology Experiments on a Macrophage System.

Authors:  Bastien Dalzon; Anaelle Torres; Julie Devcic; Daphna Fenel; Jacques-Aurélien Sergent; Thierry Rabilloud
Journal:  Front Toxicol       Date:  2021-12-06

Review 8.  Cytotoxicity of Metal-Based Nanoparticles: From Mechanisms and Methods of Evaluation to Pathological Manifestations.

Authors:  Peizheng Xiong; Xiangming Huang; Naijing Ye; Qunwen Lu; Gang Zhang; Shunlin Peng; Hongbo Wang; Yiyao Liu
Journal:  Adv Sci (Weinh)       Date:  2022-03-27       Impact factor: 17.521

9.  The Size-dependent Cytotoxicity of Amorphous Silica Nanoparticles: A Systematic Review of in vitro Studies.

Authors:  Xuemeng Dong; Zehao Wu; Xiuping Li; Liyan Xiao; Man Yang; Yang Li; Junchao Duan; Zhiwei Sun
Journal:  Int J Nanomedicine       Date:  2020-11-18

10.  Serum Lowers Bioactivity and Uptake of Synthetic Amorphous Silica by Alveolar Macrophages in a Particle Specific Manner.

Authors:  Martin Wiemann; Antje Vennemann; Cornel Venzago; Gottlieb-Georg Lindner; Tobias B Schuster; Nils Krueger
Journal:  Nanomaterials (Basel)       Date:  2021-03-03       Impact factor: 5.076

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