Literature DB >> 11853698

Modulation of apoptosis by mitochondrial uncouplers: apoptosis-delaying features despite intrinsic cytotoxicity.

Oliver J Stoetzer1, Alexei Pogrebniak, Renate Pelka-Fleischer, Max Hasmann, Wolfgang Hiddemann, Volkmar Nuessler.   

Abstract

Disruption of mitochondrial electron transport and opening of the so-called mitochondrial permeability transition pores (PTPs) are early events in apoptotic cell death and may be caused by the uncoupler of mitochondrial oxidation and phosphorylation, carbonyl cyanide p-trifluoromethoxyphenylhydrazone (FCCP). We investigated the cellular toxicity of FCCP in HL60 and CCRF-CEM cells alone or in combination with the known apoptosis inducers such as inhibitor of serine/threonine protein kinases staurosporine (Sts) and protein kinase C inhibitor chelerythrine. FCCP induced apoptotic cell death in both cell lines in a dose-dependent manner, and we were able to demonstrate an appearance of caspase-3-dependent PARP cleavage fragments with Western blot and the appearance of large (15-50 kb) DNA fragments using pulsed-field gel electrophoresis. After 2 hr of incubation with Che or Sts more than half of the cells had died by apoptosis. We observed a statistically significant delay in Sts- and Che-induced apoptotic cell death in CCRF-CEM cells when the cells were preincubated with FCCP but not with zVAD-FMK: about 50% more cells survived after pre-treatment with FCCP, as compared to 1 hr treatment with Che alone (P<0.05), and 25% more cells were alive after 6 hr of treatment, as compared to 6 hr exposure to Sts alone (P<0.05). The protective effect of FCCP was, however, transient and lasted only 6 hr. Treatment with aurintricarboxylic acid completely prevented Che- and Sts-induced apoptotic cell death in CCRF-CEM and HL60 cells. Incubation with Che resulted in a drop in the intracellular ATP content, predominantly distinctive in HL60, and in NAD(+) content in CCRF-CEM cells. Both ATP and NAD(+) drop were prevented with ATA, but not with FCCP or zVAD. Our data suggest that treatment with uncouplers of oxidative phosphorylation can induce apoptotic cell death in haematopoietic cell lines. However, when used in combination with serine/threonine protein kinase inhibitors FCCP can even prevent apoptosis.

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Year:  2002        PMID: 11853698     DOI: 10.1016/s0006-2952(01)00879-6

Source DB:  PubMed          Journal:  Biochem Pharmacol        ISSN: 0006-2952            Impact factor:   5.858


  3 in total

1.  Reduced mitochondrial coupling in vivo alters cellular energetics in aged mouse skeletal muscle.

Authors:  David J Marcinek; Kenneth A Schenkman; Wayne A Ciesielski; Donghoon Lee; Kevin E Conley
Journal:  J Physiol       Date:  2005-10-27       Impact factor: 5.182

2.  The mitochondrial respiratory chain is a modulator of apoptosis.

Authors:  Jennifer Q Kwong; Matthew S Henning; Anatoly A Starkov; Giovanni Manfredi
Journal:  J Cell Biol       Date:  2007-12-17       Impact factor: 10.539

3.  Ex Vivo Cardiotoxicity of Antineoplastic Casiopeinas Is Mediated through Energetic Dysfunction and Triggered Mitochondrial-Dependent Apoptosis.

Authors:  Christian Silva-Platas; César A Villegas; Yuriana Oropeza-Almazán; Mariana Carrancá; Alejandro Torres-Quintanilla; Omar Lozano; Javier Valero-Elizondo; Elena C Castillo; Judith Bernal-Ramírez; Evaristo Fernández-Sada; Luis F Vega; Niria Treviño-Saldaña; Héctor Chapoy-Villanueva; Lena Ruiz-Azuara; Carmen Hernández-Brenes; Leticia Elizondo-Montemayor; Carlos E Guerrero-Beltrán; Karla Carvajal; María E Bravo-Gómez; Gerardo García-Rivas
Journal:  Oxid Med Cell Longev       Date:  2018-03-25       Impact factor: 6.543

  3 in total

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