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Cytokinin-induced cell death is associated with elevated expression of alternative oxidase in tobacco BY-2 cells

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Abstract

N6-benzyladenine (BA) and N6-benzyladenosine ([9R]BA) induce massive production of reactive oxygen species (ROS) that is eventually followed by a loss of cell viability in tobacco BY-2 cells (Mlejnek et al. Plant Cell Environ 26:1723–1735, 2003, Plant Sci 168:389–395, 2005). Results presented in this work suggest that the main sources of ROS are likely mitochondria and that the maintenance of the mitochondrial transmembrane potential is crucial for ROS production in cytokinin-treaded BY-2 cells. Therefore, the possible involvement of alternative oxidase (AOX) in cell death process induced by BA and [9R]BA was studied. About three- to fourfold increase in mRNA levels of AOX1 was observed a few hours after the BA and [9R]BA addition into the growth medium. The elevated expression of AOX1 mRNA could be prevented by adding adenine and adenosine which simultaneously reduced the cytotoxic effects of BA and [9R]BA, respectively. N6-benzyladenine 7-β-d-glucoside ([7G]BA) which is a common non-toxic metabolite of BA and [9R]BA did not affect the AOX1 mRNA expression. Although AOX1 seemed to be involved in protection of BY-2 cells against the abiotic stress induced by BA and [9R]BA, the results do not support the idea that it protects cells from death exclusively by scavenging of reactive oxygen species. Indeed, N-propyl gallate, an inhibitor of AOX, decreased cell survival despite it concomitantly decreased the ROS production. This finding is in contrast to the effect of salicylhydroxamic acid, another well-known inhibitor of AOX, which also increased the number of dying cells while it increased the ROS production.

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References

  • Andrews FA, Beggs WH, Sarosi GA (1977) Influence of antioxidants on the bioactivity of amphotericin B. Antimicrob Agen Chemother 11:615–618

    Article  CAS  Google Scholar 

  • Apel K, Hirt H (2004) Reactive oxygen species: metabolism, oxidative stress, and signal transduction. Annu Rev Plant Biol 55:373–399

    Article  PubMed  CAS  Google Scholar 

  • Balk J, Leaver CJ, McCabe PF (1999) Translocation of cytochrome c from the mitochondria to the cytosol occurs during heat-induced programmed cell death in cucumber plants. FEBS Lett 463:151–154

    Article  PubMed  CAS  Google Scholar 

  • Chomczynski P, Sacchi N (1987) Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. Anal Biochem 162:156–159

    Article  PubMed  CAS  Google Scholar 

  • Clifton R, Millar AH, Whelan J (2006) Alternative oxidases in Arabidopsis: a comparative analysis of differential expression in the gene family provides new insights into function of non-phosphorylating bypasses. Biochim Biophys Acta 1757:730–741

    Article  PubMed  CAS  Google Scholar 

  • Ellis RE, Yuan JY, Horvitz HR (1991) Mechanisms and functions of cell death. Annu Rev Cell Biol 7:663–698

    Article  PubMed  CAS  Google Scholar 

  • Green D, Kroemer G (1998) The central executioners of apoptosis: caspases or mitochondria? Trends Cell Biol 8:267–271

    Article  PubMed  CAS  Google Scholar 

  • Greenberg JT (1996) Programmed cell death: a way of life for plants. Proc Natl Acad Sci U S A 93:12094–12097

    Article  PubMed  CAS  Google Scholar 

  • Hanqing F, Kun S, Mingquan L, Hongyu L, Xin L, Yan L, Yifeng W (2010) The expression, function and regulation of mitochondrial alternative oxidase under biotic stresses. Mol Plant Pathol 11:429–440

    Article  PubMed  Google Scholar 

  • LeBel CP, Ischiropoulos H, Bondy SC (1992) Evaluation of the probe 2′,7′-dichlorofluorescein as an indicator of reactive oxygen species formation and oxidative stress. Chem Res Toxicol 5:227–231

    Article  PubMed  CAS  Google Scholar 

  • Maxwell DP, Wang Y, McIntosh L (1999) Alternative oxidase: from gene to function. Lowers mitochondrial reactive oxygen production in plant cells. Proc Natl Acad Sci U S A 96:8271–8276

    Article  PubMed  CAS  Google Scholar 

  • Millar AH, Wiskich JT, Whelan J, Day DA (1993) Organic acid activation of the alternative oxidase of plant mitochondria. FEBS Lett 329:259–262

    Article  PubMed  CAS  Google Scholar 

  • Mitchell P, Moyle J (1967) Respiration-driven proton translocation in rat liver mitochondria. Biochem J 105:1147–1162

    PubMed  CAS  Google Scholar 

  • Mlejnek P, Prochazka S (2002) Caspase activation and isopentenyladenosine-induced apoptosis in tobacco BY-2 cells. Planta 215:158–166

    Article  PubMed  CAS  Google Scholar 

  • Mlejnek P, Dolezel P, Prochazka S (2003) Intracellular phosphorylation of benzyladenosine is related to apoptosis induction in tobacco BY-2 cells. Plant Cell Environ 26:1723–1735

    Article  CAS  Google Scholar 

  • Mlejnek P, Dolezel P, Prochazka S (2005) Intracellular conversion of cytokinin bases into corresponding mononucleotides is related to cell death induction in tobacco BY-2 cells. Plant Sci 168:389–395

    Article  CAS  Google Scholar 

  • Moller IM (2001) Plant mitochondria and oxidative stress: electron transport, NADPH turnover, and metabolism of reactive oxygen species. Annu Rev Plant Physiol Mol Biol 52:561–591

    Article  CAS  Google Scholar 

  • Moller IM, Berczi A, van der Plas LHW, Lambers H (1988) Measurement of the activity and capacity of the alternative pathway in intact plant tissues: identification of problems and possible solutions. Physiol Plant 72:642–649

    Article  CAS  Google Scholar 

  • Nagata T, Nemoto Y, Hasezawa S (1992) Tobacco BY-2 cell line as the “HeLa” cell line in the cell biology of higher plants. Int Rev Cytol 132:1–30

    Article  CAS  Google Scholar 

  • Noctor G, De Paepe R, Foyer CH (2007) Mitochondrial redox biology and homeostasis in plants. Trends Plant Sci 12:125–134

    Article  PubMed  CAS  Google Scholar 

  • Parrish DJ, Leopold AC (1978) Confounding of alternate respiration by lipoxygenase activity. Plant Physiol 62:470–472

    Article  PubMed  CAS  Google Scholar 

  • Parsons HL, Yip JY, Vanlerberghe GC (1999) Increased respiratory restriction during phosphate-limited growth in transgenic tobacco cells lacking alternative oxidase. Plant Physiol 121:1309–1320

    Article  PubMed  CAS  Google Scholar 

  • Rasmusson AG, Soole KL, Elthon TE (2004) Alternative NAD(P)H dehydrogenases of plant mitochondria. Annu Rev Plant Biol 55:23–39

    Article  PubMed  CAS  Google Scholar 

  • Reape TJ, McCabe PF (2010) Apoptotic-like regulation of programmed cell death in plants. Apoptosis 15:249–256

    Article  PubMed  CAS  Google Scholar 

  • Robson CA, Vanlerberghe GC (2002) Transgenic plant cells lacking mitochondrial alternative oxidase have increased susceptibility to mitochondria-dependent and -independent pathways of programmed cell death. Plant Physiol 129:1908–1920

    Article  PubMed  CAS  Google Scholar 

  • Ryerson DE, Heath MC (1996) Cleavage of nuclear DNA into oligonucleosomal fragments during cell death induced by fungal infection or by abiotic treatments. Plant Cell 8:393–402

    PubMed  CAS  Google Scholar 

  • Schonbaum GR, Bonner WD, Storey BT, Bahr JT (1971) Specific inhibition of the cyanide-insensitive respiratory pathway in plant mitochondria by hydroxamic acids. Plant Physiol 47:124–128

    Article  PubMed  CAS  Google Scholar 

  • Skulachev VP (1998) Uncoupling: new approaches to an old problem of bioenergetics. Biochim Biophys Acta 1363:100–124

    Article  PubMed  CAS  Google Scholar 

  • Van Aken O, Giraud E, Clifton R, Whelan J (2009) Alternative oxidase: a target and regulator of stress responses. Physiol Plant 137:354–361

    Article  PubMed  Google Scholar 

  • Van Breusegen F, Dat JF (2006) Reactive oxygen species in plant cell death. Plant Physiol 141:384–390

    Article  Google Scholar 

  • Vanlerberghe GC, McIntosh L (1997) Molecular biology of the alternative oxidase. Annu Rev Plant Physiol Plant Mol Biol 48:703–734

    Article  PubMed  CAS  Google Scholar 

  • Wojtaszek P (1997) Oxidative burst: an early plant response to pathogen infection. Biochem J 322:681–692

    PubMed  CAS  Google Scholar 

  • Yao N, Eisfelder BJ, Marvin J, Greenberg JT (2004) The mitochondrion—an organelle commonly involved in programmed cell death in Arabidopsis thaliana. Plant J 40:596–610

    Article  PubMed  CAS  Google Scholar 

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Acknowledgement

This work was supported by grant MSM 6198959216 (Ministry of Education, Youth and Sports). The technical help by Martina Juzova is greatly appreciated.

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The author declares that he has no conflict of interest.

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Correspondence to Petr Mlejnek.

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Handling Editor: Friedrich W. Bentrup

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Mlejnek, P. Cytokinin-induced cell death is associated with elevated expression of alternative oxidase in tobacco BY-2 cells. Protoplasma 250, 1195–1202 (2013). https://doi.org/10.1007/s00709-013-0501-3

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  • DOI: https://doi.org/10.1007/s00709-013-0501-3

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