Nanomaterial-induced cell death in pulmonary and hepatic cells following exposure to three different metallic materials: The role of autophagy and apoptosis
Allbwn ymchwil: Cyfraniad at gyfnodolyn › Erthygl › adolygiad gan gymheiriaid
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Yn: Nanotoxicology, Cyfrol 11, Rhif 2, 03.2017, t. 184-200.
Allbwn ymchwil: Cyfraniad at gyfnodolyn › Erthygl › adolygiad gan gymheiriaid
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T1 - Nanomaterial-induced cell death in pulmonary and hepatic cells following exposure to three different metallic materials
T2 - The role of autophagy and apoptosis
AU - Kermanizadeh, Ali
AU - Jantzen, Kim
AU - Ward, Michael B
AU - Durhuus, Jon Ambæk
AU - Juel Rasmussen, Lene
AU - Loft, Steffen
AU - Møller, Peter
PY - 2017/3
Y1 - 2017/3
N2 - Autophagy is the catabolic process involving the sequestration of the cytoplasm within double-membrane vesicles, which fuse with lysosomes to form autolysosomes in which autophagic targets are degraded. Since most endocytic routes of nanomaterial uptake converge upon the lysosome and the possibility that autophagy induction by NMs may be an attempt by the cell to self-preserve following the external challenge, this study investigated the role of autophagy following exposure to a panel of widely used metal-based NMs with high toxicity (Ag and ZnO) or low toxicity (TiO2) in a pulmonary (A549) and hepatic (HepG2) cell line. The in vitro exposure to the Ag and ZnO NMs resulted in the induction of both apoptosis and autophagy pathways in both cell types. However, the progression of autophagy was blocked in the formation of the autolysosome, which coincided with morphologic changes in the actin cytoskeleton. This response was not observed following the exposure to low-toxicity TiO2 NMs. Overall, the results show that high toxicity NMs can cause a dysfunction in the autophagy pathway which is associated with apoptotic cell death.
AB - Autophagy is the catabolic process involving the sequestration of the cytoplasm within double-membrane vesicles, which fuse with lysosomes to form autolysosomes in which autophagic targets are degraded. Since most endocytic routes of nanomaterial uptake converge upon the lysosome and the possibility that autophagy induction by NMs may be an attempt by the cell to self-preserve following the external challenge, this study investigated the role of autophagy following exposure to a panel of widely used metal-based NMs with high toxicity (Ag and ZnO) or low toxicity (TiO2) in a pulmonary (A549) and hepatic (HepG2) cell line. The in vitro exposure to the Ag and ZnO NMs resulted in the induction of both apoptosis and autophagy pathways in both cell types. However, the progression of autophagy was blocked in the formation of the autolysosome, which coincided with morphologic changes in the actin cytoskeleton. This response was not observed following the exposure to low-toxicity TiO2 NMs. Overall, the results show that high toxicity NMs can cause a dysfunction in the autophagy pathway which is associated with apoptotic cell death.
KW - A549 Cells
KW - Apoptosis/drug effects
KW - Autophagy/drug effects
KW - Cell Culture Techniques
KW - Hep G2 Cells
KW - Humans
KW - Liver/drug effects
KW - Lung/drug effects
KW - Lysosomes/drug effects
KW - Nanostructures/chemistry
KW - Particle Size
KW - Silver/chemistry
KW - Surface Properties
KW - Titanium/chemistry
KW - Zinc Oxide/chemistry
U2 - 10.1080/17435390.2017.1279359
DO - 10.1080/17435390.2017.1279359
M3 - Article
C2 - 28055265
VL - 11
SP - 184
EP - 200
JO - Nanotoxicology
JF - Nanotoxicology
SN - 1743-5390
IS - 2
ER -