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Biochim Biophys Acta Mol Cell Biol Lipids ; 1863(4): 379-387, 2018 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-29325722

RESUMO

The mitochondrial phospholipid cardiolipin (CL) has been implicated with mitochondrial morphology, function, and cell proliferation. Changes in CL are often paralleled by changes in the lipid environment of mitochondria that may contribute to mitochondrial function and proliferation. This study aimed to separate the effects of CL content and CL composition from cellular free fatty acid distribution on bioenergetics and proliferation in C6 glioma cells. To this end, cardiolipin synthase and the CL remodelling enzyme, tafazzin, were knocked-down by siRNA in C6 cells. After 72 h of cultivation, we analysed CL composition by means of LC/MS/MS, distribution of cellular fatty acids by means of gas chromatography, and determined oxygen consumption and proliferation. Knock-down of cardiolipin synthase affected the cellular CL content in the presence of linoleic acid (LA) in the culture medium. Knock-down of tafazzin had no consequence with respect to the pattern of cellular fatty acids but caused a decrease in cell proliferation. It significantly changed the distribution of molecular CL species, increased CL content, decreased oxygen consumption, and decreased cell proliferation when cultured in the presence of linoleic acid (LA). The addition of linoleic acid to the culture medium caused significant changes in the pattern of cellular fatty acids and the composition of molecular CL species. These data suggest that tafazzin is required for efficient bioenergetics and for proliferation of glioma cells. Supplementation of fatty acids can be a powerful tool to direct specific changes in these parameters.


Assuntos
Neoplasias Encefálicas/enzimologia , Neoplasias Encefálicas/patologia , Glioma/enzimologia , Glioma/patologia , Proteínas de Membrana/metabolismo , Mitocôndrias/metabolismo , RNA Interferente Pequeno/metabolismo , Fatores de Transcrição/metabolismo , Transferases (Outros Grupos de Fosfato Substituídos)/metabolismo , Aciltransferases , Animais , Cardiolipinas/metabolismo , Linhagem Celular Tumoral , Proliferação de Células , Citrato (si)-Sintase/metabolismo , Técnicas de Silenciamento de Genes , Ácido Linoleico/metabolismo , Proteínas de Membrana/genética , RNA Mensageiro/genética , RNA Mensageiro/metabolismo , Ratos , Transferases (Outros Grupos de Fosfato Substituídos)/genética
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