2018
DOI: 10.3390/ijms19113618
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Cytotoxicity and Transcriptomic Analysis of Silver Nanoparticles in Mouse Embryonic Fibroblast Cells

Abstract: The rapid development of nanotechnology has led to the use of silver nanoparticles (AgNPs) in biomedical applications, including antibacterial, antiviral, anti-inflammatory, and anticancer therapies. The molecular mechanism of AgNPs-induced cytotoxicity has not been studied thoroughly using a combination of cellular assays and RNA sequencing (RNA-Seq) analysis. In this study, we prepared AgNPs using myricetin, an anti-oxidant polyphenol, and studied their effects on NIH3T3 mouse embryonic fibroblasts as an in … Show more

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Cited by 72 publications
(60 citation statements)
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References 83 publications
(110 reference statements)
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“…Silver nanoparticles (AgNPs) are used as antiviral, antibacterial, anti-inflammatory, anti-angiogenesis, antiplatelet, antifungal and anticancer agents due to their unique physiochemical properties and superior biological functions [54,68,69]. Synthesis of AgNPs is carried out by various physical, chemical and biological methods.…”
Section: Silver Nanoparticlesmentioning
confidence: 99%
“…Silver nanoparticles (AgNPs) are used as antiviral, antibacterial, anti-inflammatory, anti-angiogenesis, antiplatelet, antifungal and anticancer agents due to their unique physiochemical properties and superior biological functions [54,68,69]. Synthesis of AgNPs is carried out by various physical, chemical and biological methods.…”
Section: Silver Nanoparticlesmentioning
confidence: 99%
“…Combined effects of melatonin and all-trans retinoic acid or somatostatin caused a marked reduction in mitochondrial membrane potential and intracellular ATP production, inducing necrotic cell death [52]. Several metal nanoparticles are known to impair ATP synthesis in mouse embryonic fibroblast cells and human colon cancer cells [80,81], while platinum decreased ATP levels in human alveolar basal epithelial cells [36]. Zhao et al [82] reported that titanium dioxide nanoparticles induced mitochondrial dynamic imbalance in HT22 cells, eventually causing mitochondrial dysfunctions and decreased level of ATP synthesis.…”
Section: Pdnps + Mlt Caused Mitochondrial Dysfunctionsmentioning
confidence: 99%
“…Cells exposed to PdNPs and MLT separately and cells exposed to PdNPs + MLT exhibited severe oxidative damage to both DNA and RNA through the accumulation of 8-OHdG and 8-OHG. Similarly, silver nanoparticles caused severe oxidative damage to DNA and accumulation of 8-OHdG and 8-OHG in embryonic fibroblast cells of mice [80], while TiO 2 NP induced ROS-mediated oxidative stress, the activation of p53, Bax, and caspase-3, and caused oxidative DNA damage in HEK-293 cells [93]. Likewise, human hepatocyte and embryonic kidney cells exposed to zinc oxide NPs (ZnONPs) showed altered cell morphology, mitochondrial dysfunction, increase of oxidative stress markers, and oxidative DNA damage [94].…”
Section: Pdnps + Mlt Induced Apoptosis and Oxidative Dna Damagementioning
confidence: 99%
“…13 A lower level of ROS is involved in the regulation of various cellular functions, while cell death is induced by higher levels of ROS. [14][15][16] Viability of Lemna gibba plant cells reduces after silver NP treatment, which is also significantly correlated with intracellular ROS induction. 16 RNA degradation can be rapidly triggered by cell death.…”
Section: Influence Of Nanoparticle Treatment On H Perforatummentioning
confidence: 97%