Interactions of Zinc Oxide Nanostructures with Mammalian Cells: Cytotoxicity and Photocatalytic Toxicity.
Chengzhu LiaoYuming JinYu-Chao LiSie Chin TjongPublished in: International journal of molecular sciences (2020)
This article presents a state-of-the-art review and analysis of literature studies on the morphological structure, fabrication, cytotoxicity, and photocatalytic toxicity of zinc oxide nanostructures (nZnO) of mammalian cells. nZnO with different morphologies, e.g., quantum dots, nanoparticles, nanorods, and nanotetrapods are toxic to a wide variety of mammalian cell lines due to in vitro cell-material interactions. Several mechanisms responsible for in vitro cytotoxicity have been proposed. These include the penetration of nZnO into the cytoplasm, generating reactive oxygen species (ROS) that degrade mitochondrial function, induce endoplasmic reticulum stress, and damage deoxyribonucleic acid (DNA), lipid, and protein molecules. Otherwise, nZnO dissolve extracellularly into zinc ions and the subsequent diffusion of ions into the cytoplasm can create ROS. Furthermore, internalization of nZnO and localization in acidic lysosomes result in their dissolution into zinc ions, producing ROS too in cytoplasm. These ROS-mediated responses induce caspase-dependent apoptosis via the activation of B-cell lymphoma 2 (Bcl2), Bcl2-associated X protein (Bax), CCAAT/enhancer-binding protein homologous protein (chop), and phosphoprotein p53 gene expressions. In vivo studies on a mouse model reveal the adverse impacts of nZnO on internal organs through different administration routes. The administration of ZnO nanoparticles into mice via intraperitoneal instillation and intravenous injection facilitates their accumulation in target organs, such as the liver, spleen, and lung. ZnO is a semiconductor with a large bandgap showing photocatalytic behavior under ultraviolet (UV) light irradiation. As such, photogenerated electron-hole pairs react with adsorbed oxygen and water molecules to produce ROS. So, the ROS-mediated selective killing for human tumor cells is beneficial for cancer treatment in photodynamic therapy. The photoinduced effects of noble metal doped nZnO for creating ROS under UV and visible light for killing cancer cells are also addressed.
Keyphrases
- reactive oxygen species
- visible light
- quantum dots
- cell death
- dna damage
- endoplasmic reticulum stress
- binding protein
- oxide nanoparticles
- oxidative stress
- induced apoptosis
- photodynamic therapy
- reduced graphene oxide
- mouse model
- cell cycle arrest
- systematic review
- single cell
- type diabetes
- sensitive detection
- room temperature
- amino acid
- diffuse large b cell lymphoma
- dna repair
- genome wide
- highly efficient
- circulating tumor
- adipose tissue
- radiation therapy
- signaling pathway
- transcription factor
- radiation induced
- endothelial cells
- small molecule
- ionic liquid
- water soluble
- skeletal muscle
- gold nanoparticles
- insulin resistance
- cell proliferation
- case control
- electron transfer
- ultrasound guided
- energy transfer
- high fat diet induced