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Modulation of pro-apoptotic effects and mitochondrial potential on B16F10 cells by DODAC/PHO-S liposomes.
Luna, Arthur Cássio de Lima; Santos Filho, José Roberto de Assis; Hesse, Henrique; Neto, Salvador Claro; Chierice, Gilberto Orivaldo; Maria, Durvanei Augusto.
Afiliação
  • Luna ACL; Biochemistry and Biophysical Laboratory, Butantan Institute, 1500, Vital Brasil Avenue, Sao Paulo, 05503-900, Brazil.
  • Santos Filho JRA; Department of Medical Sciences, Medical School, University of Sao Paulo, Sao Paulo, Brazil.
  • Hesse H; Biochemistry and Biophysical Laboratory, Butantan Institute, 1500, Vital Brasil Avenue, Sao Paulo, 05503-900, Brazil.
  • Neto SC; Biochemistry and Biophysical Laboratory, Butantan Institute, 1500, Vital Brasil Avenue, Sao Paulo, 05503-900, Brazil.
  • Chierice GO; Department of Chemistry and Molecular Physics, University of Sao Paulo, Sao Carlos, Brazil.
  • Maria DA; Department of Chemistry and Molecular Physics, University of Sao Paulo, Sao Carlos, Brazil.
BMC Res Notes ; 11(1): 126, 2018 Feb 14.
Article em En | MEDLINE | ID: mdl-29444697
OBJECTIVE: We aimed to evaluate the potential of DODAC/PHO-S liposomes on the modulation of the expression of pro-apoptotic proteins, loss of lysosomal integrity and the mitochondrial electrical potential, compared with phosphoethanolamine. RESULTS: The results of this study demonstrate that DODAC/PHO-S liposomes have exhibited broad cytotoxic potential in B16F10 murine melanoma cells, with significantly greater proportions than treatment with PHO-S. The treatment with the DODAC/PHO-S 2.0 mM liposomal formulation was more efficient in decreasing mitochondrial electrical potential at the same concentrations and treatment time than PHO-S The liposomal formulation DODAC/PHO-S (2.0 mM) was more efficient to promote morphological changes in the cells, without presenting intact lysosomes, at the same time of treatment and concentration as PHO-S Our results demonstrated that the liposomal formulation increased DR4 receptor expression and activated caspases 8 and 3, resulting in the release of cytochrome c in B16F10 tumour cells, when compared to treatment with PHO-S The data obtained prove that the use of DODAC as carrier can maximize the cytotoxic effects of PHO-S This was demonstrated by the translocation of cytochrome c to the cytoplasm and activation of caspase-3 and 8, decreasing the mitochondrial electrical potential and generating morphological changes, in B16F10 cells.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Melanoma Experimental / Adjuvantes Imunológicos / Apoptose / Citotoxinas / Etanolaminas / Compostos de Amônio Quaternário / Lipossomos / Mitocôndrias Limite: Animals Idioma: En Revista: BMC Res Notes Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Brasil País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Melanoma Experimental / Adjuvantes Imunológicos / Apoptose / Citotoxinas / Etanolaminas / Compostos de Amônio Quaternário / Lipossomos / Mitocôndrias Limite: Animals Idioma: En Revista: BMC Res Notes Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Brasil País de publicação: Reino Unido