4.7 Article

Coenzyme Q Protects Cells Against Serum Withdrawal-Induced Apoptosis by Inhibition of Ceramide Release and Caspase-3 Activation

Journal

ANTIOXIDANTS & REDOX SIGNALING
Volume 2, Issue 2, Pages 263-275

Publisher

MARY ANN LIEBERT, INC
DOI: 10.1089/ars.2000.2.2-263

Keywords

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Funding

  1. Spanish Direction General de Educacion Superior [PB98-0329-C02-01]
  2. Junta de Andalucia
  3. Spanish Government Ministerio de Educacion y Cultura

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Coenzyme Q(10) (CoQ(10)) is a component of the antioxidant machinery that protects cell membranes from oxidative damage and decreases apoptosis in leukemic cells cultured in serum-depleted media. Serum deprivation induced apoptosis in CEM-C7H2 (CEM) and to a lesser extent in CEM-9F3, a subline overexpressing Bcl-2. Addition of CoQ(10) to serum-free media decreased apoptosis in both cell lines. Serum withdrawal induced an early increase of neutral-sphingomyelinase activity, release of ceramide, and activation of caspase-3 in both cell lines, but this effect was more pronounced in C E M cells. CoQ(10) prevented activation of this cascade of events. Lipids extracted from serum-depleted cultures activated caspase-3 independently of the presence of mitochondria in cell-free in vitro assays. Activation of caspase-3 by lipid extracts or ceramide was prevented by okadaic acid, indicating the implication of a phosphatase in this process. Our results support the hypothesis that plasma membrane CoQ(10) regulate the initiation phase of serum withdrawal-induced apoptosis by preventing oxidative damage and thus avoiding activation of downstream effectors as neutral-sphingomyelinase and subsequent ceramide release and caspase activation pathways. Antiox. Redox Signal. 2, 263-275.

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