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Gold nanoparticles do not induce myotube cytotoxicity but increase the susceptibility to cell death.
Leite, Paulo Emílio Corrêa; Pereira, Mariana Rodrigues; do Nascimento Santos, Carlos Antonio; Campos, Andrea Porto Carreiro; Esteves, Ticiana Mota; Granjeiro, José Mauro.
Afiliación
  • Leite PE; Divisão de Biologia Celular e Bioengenharia, Diretoria de Metrologia Aplicada as Ciências da Vida (DIMAV), Brazil. Electronic address: leitepec@gmail.com.
  • Pereira MR; Instituto de Biologia, Universidade Federal Fluminense, Niterói, RJ, Brazil.
  • do Nascimento Santos CA; Divisão de Biologia Celular e Bioengenharia, Diretoria de Metrologia Aplicada as Ciências da Vida (DIMAV), Brazil.
  • Campos AP; Divisão de Metrologia de Materiais (DIMAT), Instituto Nacional de Metrologia, Qualidade e Tecnologia (INMETRO), 25250-020 Duque de Caxias, RJ, Brazil.
  • Esteves TM; Divisão de Biologia Celular e Bioengenharia, Diretoria de Metrologia Aplicada as Ciências da Vida (DIMAV), Brazil.
  • Granjeiro JM; Divisão de Biologia Celular e Bioengenharia, Diretoria de Metrologia Aplicada as Ciências da Vida (DIMAV), Brazil; Instituto de Biologia, Universidade Federal Fluminense, Niterói, RJ, Brazil.
Toxicol In Vitro ; 29(5): 819-27, 2015 Aug.
Article en En | MEDLINE | ID: mdl-25790728
Gold nanoparticles (AuNP) have been widely used for many applications, including as biological carriers. A better understanding concerning AuNP safety on muscle cells is crucial, since it could be a potential tool in the nanomedicine field. Here, we describe the impact of polyethylene glycol-coated gold nanoparticles (PEG-AuNP) interaction with differentiated skeletal muscle C2C12 cells on cell viability, mitochondria function, cell signaling related to survival, cytokine levels and susceptibility to apoptosis. Intracellular localization of 4.5 nm PEG-AuNP diameter size was evidenced by STEM-in-SEM in myotube cells. Methods for cytotoxicity analysis showed that PEG-AuNP did not affect cell viability, but intracellular ATP levels and mitochondrial membrane potential increased. Phosphorylation of ERK was not altered but p-AKT levels reduced (p<0.01). Pre-treatment of cells with PEG-AuNP followed by staurosporine induction increased the caspases-3/7 activity. Indeed, cytokines analysis revealed a sharp increase of IFN-γ and TGF-ß1 levels after PEG-AuNP treatment, suggesting that inflammatory and fibrotic phenotypes process were activated. These data demonstrate that PEG-AuNP affect the myotube physiology leading these cells to be more susceptible to death stimuli in the presence of staurosporine. Altogether, these results present evidence that PEG-AuNP affect the susceptibility to apoptosis of muscle cells, contributing to development of safer strategies for intramuscular delivery.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fibras Musculares Esqueléticas / Nanopartículas del Metal / Oro Límite: Animals Idioma: En Revista: Toxicol In Vitro Asunto de la revista: TOXICOLOGIA Año: 2015 Tipo del documento: Article Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fibras Musculares Esqueléticas / Nanopartículas del Metal / Oro Límite: Animals Idioma: En Revista: Toxicol In Vitro Asunto de la revista: TOXICOLOGIA Año: 2015 Tipo del documento: Article Pais de publicación: Reino Unido