Research letter
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mtDNA‐depleted U937 cells are sensitive to TNF and Fas‐mediated cytototxicity

Susana Gamen

Departamento de Bioquímica y Biología Molecular, Facultad de Ciencias, Universidad de Zaragoza, 50009 Zaragoza, Spain

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Alberto Anel

Departamento de Bioquímica y Biología Molecular, Facultad de Ciencias, Universidad de Zaragoza, 50009 Zaragoza, Spain

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Julio Montoya

Facultad de Veterinaria, Universidad de Zaragoza, 50009 Zaragoza, Spain

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Isabel Marzo

Departamento de Bioquímica y Biología Molecular, Facultad de Ciencias, Universidad de Zaragoza, 50009 Zaragoza, Spain

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Andrés Piñeiro

Departamento de Bioquímica y Biología Molecular, Facultad de Ciencias, Universidad de Zaragoza, 50009 Zaragoza, Spain

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Javier Naval

E-mail address:jnaval@msf.unizar.es

Departamento de Bioquímica y Biología Molecular, Facultad de Ciencias, Universidad de Zaragoza, 50009 Zaragoza, Spain

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First published: November 27, 1995
Cited by: 19
Corresponding author. Fax: (34) (76) 76-1159.

Abstract

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‐ϱ°) were resistant to TNF, but this was due to the loss of its 55 kDa receptor. U937‐ϱ° 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.

Number of times cited: 19

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