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Merck

mtDNA-depleted U937 cells are sensitive to TNF and Fas-mediated cytotoxicity.

FEBS letters (1995-11-27)
S Gamen, A Anel, J Montoya, I Marzo, A Piñeiro, J Naval
RESUMO

It has been proposed that TNF cytotoxicity is mediated by reactive oxygen intermediates generated by uncoupling of mitochondrial respiration. We have compared sensitive U937 cells and derived cell lines depleted of mtDNA for their ability to undergo TNF- and Fas-induced apoptosis. Cells lacking around 98% of mtDNA were still sensitive to TNF-induced apoptosis. U937 cells devoid of mtDNA (U937-rho degree) were resistant to TNF, but this was due to the loss of its 55 kDa receptor. U937-rho degree cells were also resistant to docosahexaenoic acid, which causes U937 cell death by lipid peroxidation. These cells were sensitive to anti-Fas toxicity. The results indicate that TNF and Fas-induced toxicity occurs by a mechanism mostly independent of mitochondrial free radical generation.

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Sigma-Aldrich
Anticorpo antiFas (humano, ativador), clone CH11, clone CH11, Upstate®, from mouse
Sigma-Aldrich
Monoclonal Anti-Rabbit Immunoglobulins–FITC antibody produced in mouse, clone RG-16, purified immunoglobulin, buffered aqueous solution