In vitro toxicity screening of amorphous silica nanoparticles using mitochondrial fraction exposure followed by MS-based proteomic analysis. Issue 16 (18th July 2022)

• Record Type: Journal Article
• Authors: Kumarathasan, Premkumari; Nazemof, Nazila; Breznan, Dalibor; Blais, Erica; Aoki, Hiroyuki; Gomes, James; Vincent, Renaud; Phanse, Sadhna; Babu, Mohan
• Is Part Of: Analyst. Volume 147:Issue 16(2022)
• Page Start: 3692
• Page End: 3708
• Publication Date: 2022-07-18
• Subjects: Chemistry, Analytic -- Periodicals; 543
• DOI: 10.1039/d2an00569g
• Languages: English
• ISSNs: 0003-2654

Abstract

Abstract : Application of mitochondrial proteomic analysis in toxicity screening of amorphous silica nanoforms. Concordance between SiNP exposure-related perturbations in mitochondrial proteins and cellular ATP responses. Abstract : Silica nanoparticles (SiNPs) are used in consumer products, engineering and medical technologies. Attractive properties of SiNPs ( e.g. size/surface-modification) enhance usage and thus the likelihood of environmental/human exposures. The assessment of health risks associated with exposures to SiNPs requires information on their relative potencies and toxicity mechanisms. In this work, phagocytic J774 cells were exposed to amorphous pristine (15, 30, 75 nm) and surface-modified (–NH2, –C3COOH, –C11COOH, –PEG) SiNP variants, and internalization was assessed by transmission electron microscopy (TEM), while cellular ATP was measured as a cytotoxicity endpoint. Furthermore, mitochondrial fractions from J774 cells were exposed to these SiNP variants (5, 15 μg mL −1 ), as well as two reference particles (SiNP 12 nm and TiO2 ), and proteomic changes were analyzed by mass spectrometry. Ingenuity Pathway Analysis was used to identify toxicity pathways. TEM analyses showed SiNP internalization and distribution along with some changes in mitochondrial structure. SiNP size- and surface-modification and chemical composition-related changes in mitochondrial proteins, including key proteins of the respiratory complex and oxidative stress, were evident based on high content mass spectrometry data. In addition, the dose-related decrease in cellular ATP levels in SiNP-exposed cells was consistent with related mitochondrial protein profiles. These findings suggest that physicochemical properties can be determinants of SiNP exposure-related mitochondrial effects, and mitochondrial exposures combined with proteomic analysis can be valuable as a new approach methodology in the toxicity screening of SiNPs for risk assessment, with added insight into related toxicity mechanisms.