Mechanisms of silver nanoparticle-induced toxicity and important role of autophagy

Bin Hsu Mao, Jui-Chen Tsai, Chun Wan Chen, Shian-Jang Yan, Ying-Jan Wang

Research output: Contribution to journalReview article

42 Citations (Scopus)

Abstract

Safety concerns have been raised over the extensive applications of silver nanoparticles (AgNPs) because nano dimensions make them highly bioactive, being potentially harmful to the exposed humans. Surface physico-chemistry (shape, surface charge, chemical composition, etc.) that mainly dictates nano-bio interactions is relevant for influencing their biocompatibility and toxicity. Although the hazardousness of AgNPs has been demonstrated in vitro and in vivo, mechanistic understanding of the toxicity particularly at the molecular and organismal levels, in addition to oxidative stress and silver ion dissolution, has remained unclear. A growing body of research has elucidated that autophagy, being activated in response to exposure to various nanomaterials, may serve as a cellular defense mechanism against nanotoxicity. Recently, autophagy activation was shown to correlate with AgNPs exposure; however, the subsequent autophagosome–lysosome fusion was defective. As autophagy plays a crucial role in selective removal of stress-mediated protein aggregates and injured organelles, AgNPs-induced autophagic flux defect may consequently lead to aggravated cytotoxic responses. Furthermore, we suggest that p62 accumulation resulting from defective autophagy may also potentially account for AgNPs cytotoxicity. Intriguingly, AgNPs have been shown to interfere with ubiquitin modifications, either via upregulating levels of enzymes participating in ubiquitination, or through impairing the biological reactivity of ubiquitin (due to formation of AgNPs-ubiquitin corona). Ubiquitination both confers selectivity to autophagy as well as modulates stabilization, activation, and trafficking of proteins involved in autophagic clearance pathways. In this regard, we offer a new perspective that interference of AgNPs with ubiquitination may account for AgNPs-induced defective autophagy and cytotoxic effects.

Original languageEnglish
Pages (from-to)1021-1040
Number of pages20
JournalNanotoxicology
Volume10
Issue number8
DOIs
Publication statusPublished - 2016 Sep 13

Fingerprint

Autophagy
Ubiquitin
Silver
Nanoparticles
Toxicity
Chemical activation
Proteins
Oxidative stress
Ubiquitination
Cytotoxicity
Surface charge
Surface chemistry
Biocompatibility
Nanostructured materials
Dissolution
Fusion reactions
Enzymes
Stabilization
Fluxes
Defects

All Science Journal Classification (ASJC) codes

  • Biomedical Engineering
  • Toxicology

Cite this

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abstract = "Safety concerns have been raised over the extensive applications of silver nanoparticles (AgNPs) because nano dimensions make them highly bioactive, being potentially harmful to the exposed humans. Surface physico-chemistry (shape, surface charge, chemical composition, etc.) that mainly dictates nano-bio interactions is relevant for influencing their biocompatibility and toxicity. Although the hazardousness of AgNPs has been demonstrated in vitro and in vivo, mechanistic understanding of the toxicity particularly at the molecular and organismal levels, in addition to oxidative stress and silver ion dissolution, has remained unclear. A growing body of research has elucidated that autophagy, being activated in response to exposure to various nanomaterials, may serve as a cellular defense mechanism against nanotoxicity. Recently, autophagy activation was shown to correlate with AgNPs exposure; however, the subsequent autophagosome–lysosome fusion was defective. As autophagy plays a crucial role in selective removal of stress-mediated protein aggregates and injured organelles, AgNPs-induced autophagic flux defect may consequently lead to aggravated cytotoxic responses. Furthermore, we suggest that p62 accumulation resulting from defective autophagy may also potentially account for AgNPs cytotoxicity. Intriguingly, AgNPs have been shown to interfere with ubiquitin modifications, either via upregulating levels of enzymes participating in ubiquitination, or through impairing the biological reactivity of ubiquitin (due to formation of AgNPs-ubiquitin corona). Ubiquitination both confers selectivity to autophagy as well as modulates stabilization, activation, and trafficking of proteins involved in autophagic clearance pathways. In this regard, we offer a new perspective that interference of AgNPs with ubiquitination may account for AgNPs-induced defective autophagy and cytotoxic effects.",
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Mechanisms of silver nanoparticle-induced toxicity and important role of autophagy. / Mao, Bin Hsu; Tsai, Jui-Chen; Chen, Chun Wan; Yan, Shian-Jang; Wang, Ying-Jan.

In: Nanotoxicology, Vol. 10, No. 8, 13.09.2016, p. 1021-1040.

Research output: Contribution to journalReview article

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AU - Mao, Bin Hsu

AU - Tsai, Jui-Chen

AU - Chen, Chun Wan

AU - Yan, Shian-Jang

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