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Environ Toxicol Pharmacol ; 86: 103654, 2021 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-33823299

RESUMO

The increasing use of metal oxide nanoparticles (MONPs) as TiO2 NPs or ZnO NPs has led to environmental release and human exposure. The respiratory system, effects on lamellar bodies and surfactant protein A (SP-A) of pneumocytes, can be importantly affected. Exposure of human alveolar epithelial cells (A549) induced differential responses; a higher persistence of TiO2 in cell surface and uptake (measured by Atomic Force Microscopy) and sustained inflammatory response (by means of TNF-α, IL-10, and IL-6 release) and ROS generation were observed, whereas ZnO showed a modest response and low numbers in cell surface. A reduction in SP-A levels at 24 h of exposure to TiO2 NPs (concentration-dependent) or ZnO NPs (the higher concentration) was also observed, reversed by blocking the inflammatory response (by the inhibition of IL-6). Loss of SP-A represents a relevant target of MONPs-induced inflammatory response that could contribute to cellular damage and loss of lung function.


Assuntos
Células Epiteliais Alveolares/efeitos dos fármacos , Nanopartículas/toxicidade , Proteína A Associada a Surfactante Pulmonar/antagonistas & inibidores , Titânio/toxicidade , Óxido de Zinco/toxicidade , Células A549 , Células Epiteliais Alveolares/metabolismo , Sobrevivência Celular/efeitos dos fármacos , Citocinas/metabolismo , Humanos , Inflamação/induzido quimicamente , Inflamação/metabolismo , Pulmão , Proteína A Associada a Surfactante Pulmonar/metabolismo , Espécies Reativas de Oxigênio/metabolismo
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