Zinc ferrite nanoparticles activate IL-1b, NFKB1, CCL21 and NOS2 signaling to induce mitochondrial dependent intrinsic apoptotic pathway in WISH cells

• Published in: Toxicology and applied pharmacology Vol. 273; no. 2; pp. 289 - 297
• Main Authors: Saquib, Quaiser, Al-Khedhairy, Abdulaziz A., Ahmad, Javed, Siddiqui, Maqsood A., Dwivedi, Sourabh, Khan, Shams T., Musarrat, Javed
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.12.2013
• Subjects: 60 APPLIED LIFE SCIENCES; Amnion - drug effects; Amnion - metabolism; Amnion - pathology; APOPTOSIS; Apoptosis - drug effects; Apoptosis - physiology; CELL CYCLE; Chemokine CCL21 - metabolism; CYTOPLASM; Cytotoxicity; DNA; DNA damage; Dose-Response Relationship, Drug; Epithelial Cells - drug effects; Epithelial Cells - metabolism; Epithelial Cells - pathology; Ferric Compounds - toxicity; FERRITE; FETAL MEMBRANES; GENES; Humans; INFLAMMATION; Interleukin-1beta - metabolism; MESSENGER-RNA; Metal Nanoparticles - toxicity; MITOCHONDRIA; Mitochondria - drug effects; Mitochondria - metabolism; Mitochondria - pathology; Nanoparticles; NANOSTRUCTURES; NF-kappa B p50 Subunit - metabolism; Nitric Oxide Synthase Type II - metabolism; OXIDATION; Oxidative stress; Particle Size; Reactive Oxygen Species - metabolism; STRAND BREAKS; STRESSES; TOXICITY; ZINC; Zinc - toxicity; Zinc ferrite; Nanoparticles; Oxidative stress; Cytotoxicity; Zinc ferrite; DNA damage; Apoptosis
• ISSN: 0041-008X; 1096-0333
• DOI: 10.1016/j.taap.2013.09.001

The present study has demonstrated the translocation of zinc ferrite nanoparticles (ZnFe2O4-NPs) into the cytoplasm of human amnion epithelial (WISH) cells, and the ensuing cytotoxicity and genetic damage. The results suggested that in situ NPs induced oxidative stress, alterations in cellular membrane and DNA strand breaks. The [3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide] (MTT) and neutral red uptake (NRU) cytotoxicity assays indicated 64.48±1.6% and 50.73±2.1% reduction in cell viability with 100μg/ml of ZnFe2O4-NPs exposure. The treated WISH cells exhibited 1.2-fold higher ROS level with 0.9-fold decline in membrane potential (ΔΨm) and 7.4-fold higher DNA damage after 48h of ZnFe2O4-NPs treatment. Real-time PCR (qPCR) analysis of p53, CASP 3 (caspase-3), and bax genes revealed 5.3, 1.6, and 14.9-fold upregulation, and 0.18-fold down regulation of bcl 2 gene vis-à-vis untreated control. RT2 Profiler™ PCR array data elucidated differential up-regulation of mRNA transcripts of IL-1b, NFKB1, NOS2 and CCL21 genes in the range of 1.5 to 3.7-folds. The flow cytometry based cell cycle analysis suggested the transfer of 15.2±2.1% (p<0.01) population of ZnFe2O4-NPs (100μg/ml) treated cells into apoptotic phase through intrinsic pathway. Over all, the data revealed the potential of ZnFe2O4-NPs to induce cellular and genetic toxicity in cells of placental origin. Thus, the significant ROS production, reduction in ΔΨm, DNA damage, and activation of genes linked to inflammation, oxidative stress, proliferation, DNA damage and repair could serve as the predictive toxicity and stress markers for ecotoxicological assessment of ZnFe2O4-NPs induced cellular and genetic damage. •First report on the molecular toxicity of ZnFe2O4-NPs in cells of placental origin•WISH cells treated with ZnFe2O4-NPs exhibited cytoplasmic localization of NPs.•ZnFe2O4-NPs induce DNA damage and mitochondrial dysfunction in WISH cells.•ZnFe2O4-NPs activate inflammatory and oxidative stress signaling in WISH cells.•Elevation of p53, CASP 3, bax and bcl 2 genes affirms intrinsic apoptotic pathway.