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Biochemistry & Molecular Biology

Effects of extracellular ATP on local and systemic responses of bean (Phaseolus vulgaris L) leaves to wounding

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Pages 417-428 | Received 05 Jul 2018, Accepted 01 Nov 2018, Published online: 20 Nov 2018

References

  • Khakh BS, Burnstock G. The double life of ATP. Sci Am. 2009;301(6):84–92.
  • Choi J, Tanaka K, Cao Y, et al. Identification of a plant receptor for extracellular ATP. Science. 2014;343(6168):290–294.
  • Chivasa S, Simon WJ, Murphy AM, et al. The effects of extracellular adenosine 5ʹ-triphosphate on the tobacco proteome. Proteomics. 2010;10(2):235–244.
  • Demidchik V, Nichols C, Oliynyk M, et al. Is ATP a signaling agent in plants? Plant Physiol. 2003;133(2):456–461.
  • Demidchik V, Shang Z, Shin R, et al. Plant extracellular ATP signalling by plasma membrane NADPH oxidase and Ca2+ channels. Plant J. 2009;58(6):903–913.
  • Demidchik V, Cuin TA, Svistunenko D, et al. Arabidopsis root k+-efflux conductance activated by hydroxyl radicals: single-channel properties, genetic basis and involvement in stress–induced cell death. J Cell Sci. 2010;123(9):1468–1479.
  • Sun J, Zhang C, Zhang X, et al. Extracellular ATP signaling and homeostasis in plant cells. Plant Signal Behav. 2012;7(5):566–569.
  • Miller G, Schlauch K, Tam R, et al. The plant NADPH oxidase RBOHD mediates rapid systemic signaling in response to diverse stimuli. Sci Signal. 2009;2(84):ra45.
  • Suzuki N, Miller G, Salazar C, et al. Temporal-spatial interaction between reactive oxygen species and abscisic acid regulates rapid systemic acclimation in plants. Plant Cell. 2013;25(9):3553–3569.
  • Gilroy S, Suzuki N, Miller G, et al. A tidal wave of signals: calcium and ROS at the forefront of rapid systemic signaling. Trends Plant Sci. 2014;19(10):623–630.
  • Reymond P, Weber H, Damond M, et al. Differential gene expression in response to mechanical wounding and insect feeding in Arabidopsis. Plant Cell. 2000;12(5):707–720.
  • Bourtsala A, Farmaki T, Galanopoulou D. Phospholipases dα and δ are involved in local and systemic wound responses of cotton (g. hirsutum). Biochem Biophys Reports. 2017;9(C):133–139.
  • Constabel CP, Bergey DR, Ryan CA. Systemin activates synthesis of wound-inducible tomato leaf polyphenol oxidase via the octadecanoid defense signaling pathway. Proc Natl Acad Sci USA. 1995;92(2):407–411.
  • Constabel CP, Ryan CA. A survey of wound–and methyl jasmonate–induced leaf polyphenol oxidase in crop plants. Phytochemistry. 1998;47(4):507–511.
  • De Bruxelles GL, Roberts MR. Signals regulating multiple responses to wounding and herbivores. Crit Rev Plant Sci. 2001;20(5):487–521.
  • León J, Sánchez-Serrano JJ. Wound signalling in plants. J Exp Bot. 2001;52(354):1–9.
  • Ryan CA, Moura DS. Systemic wound signaling in plants: a new perception. Proc Natl Acad Sci USA. 2002;99(10):6519–6520.
  • Tanaka K, Gilroy S, Jones AM, et al. Extracellular ATP signaling in plants. Trends Cell Biol. 2010;20(10):601–608.
  • Tanaka K, Choi J, Cao Y, et al. Extracellular ATP acts as a damage–associated molecular pattern (damp) signal in plants. Front Plant Sci. 2014;5:446.
  • Chivasa S, Murphy AM, Hamilton JM, et al. Extracellular ATP is a regulator of pathogen defence in plants. Plant J. 2009;60(3):436–448.
  • Chivasa S, Ndimba B, Simon W. Extracellular ATP functions as an endogenous external metabolite regulating plant cell viability. Plant Cell. 2005;17(11):3019–3034.
  • Achary VMM, Panda BB. Aluminium–induced DNA damage and adaptive response to genotoxic stress in plant cells are mediated through reactive oxygen intermediates. Mutagenesis. 2010;25(2):201–209.
  • Zhou Q. The measurement of malondialdehyde in plants. In: Zhou Q, editor. Methods in plant physiol. Beijing: China Agricultural Press; 2001. p. 173–174.
  • Aebi H. Catalase. In: Bergmeyer HU, editor. Methods of enzymatic analysis. New York: Academic Press; 1974. p. 673–677.
  • Liu J, Tian S, Meng X, et al. Effects of chitosan on control of postharvest diseases and physiological responses of tomato fruit. Postharvest Biol Tec. 2007;44(3):300–306.
  • Wu S, Peiffer M, Luthe DS, et al. ATP hydrolyzing salivary enzymes of caterpillars suppress plant defenses. PLoS One. 2012;7(7):e41947.
  • Ayala A, Muñoz MF, Argüelles S. Lipid peroxidation: production, metabolism, and signaling mechanisms of malondialdehyde and 4–hydroxy–2–nonenal. Oxid Med Cell Longev. 2014;2014(6):360–438.
  • Hu ZH, Shen YB, Shen FY, et al. Effects of feeding Clostera anachoreta, on hydrogen peroxide accumulation and activities of peroxidase, catalase, and ascorbate peroxidase in populus simonii × P.pyramidalis,‘opera 8277ʹ leaves. Acta Physiol Plant. 2009;31(5):995–1002.
  • Orozco-Cárdenas M, Ryan CA. Hydrogen peroxide is generated systemically in plant leaves by wounding and systemin via the octadecanoid pathway. Proc Natl Acad Sci USA. 1999;96(11):6553–6557.
  • Orozcocárdenas ML, Narváezvásquez J, Ryan CA. Hydrogen peroxide acts as a second messenger for the induction of defense genes in tomato plants in response to wounding, systemin, and methyl jasmonate. Plant Cell. 2001;13(1):179–191.
  • Ślesak I, Ślesak H, Libik M, et al. Antioxidant response system in the short -term post-wounding effect in Mesembryanthemum crystallinum leaves. J Plant Physiol. 2008;165(2):127–137.
  • Kim SY, Sivaguru M, Stacey G. Extracellular ATP in plants. visualization, localization and analysis of physiological significance in growth and signaling. Plant Physiol. 2006;142(3):984–992.
  • Lim MH, Wu J, Yao J, et al. Apyrase suppression raises extracellular ATP levels and induces gene expression and cell wall changes characteristic of stress responses. Plant Physiol. 2014;164(4):2054–2067.
  • Song CJ, Roux SJ. Extracellular ATP induces the accumulation of superoxide via NADPH oxidases in Arabidopsis. Plant Physiol. 2006;140(4):1222–1232.
  • Rieder B, Neuhaus HE. Identification of an Arabidopsis plasma membrane -located ATP transporter important for anther development. Plant Cell. 2011;23(5):1932–1944.
  • Thomas C, Rajagopal A, Windsor B, et al. A role for ectophosphatase in xenobiotic resistance. Plant Cell. 2000;12(4):519–533.
  • Togo T, Krasieva TB, Steinhardt RA. A decrease in membrane tension precedes successful cell- membrane repair. Mol Biol Cell. 2000;11(12):4339–4346.
  • Sonnemann KJ, Bement WM. Wound repair: toward understanding and integration of single-cell and multicellular wound responses. Annu Rev Cell Dev Biol. 2011;27:237–263.
  • Maruta T, Inoue T, Tamoi M, et al. Arabidopsis NADPH oxidases, AtrbohD and AtrbohF, are essential for jasmonic acid-induced expression of genes regulated by MYC2 transcription factor. Plant Sci. 2011;180(4):655–660.
  • Thompson JE, Legge RL, Barber RF. The role of free radicals in senescence and wounding. New Phytol. 2010;105(3):317–344.
  • Liavonchanka A, Feussner I. Lipoxygenases: occurrence, functions and catalysis. J Plant Physiol. 2006;163(3):348–357.
  • Yang HR, Tang K, Liu HT, et al. Effect of salicylic acid on jasmonic acid–related defense response of pea seedlings to wounding. Sci Hortic. 2011;128(3):166–173.
  • Chandru HK, Kim E, Kuk Y, et al. Kinetics of wound–induced activation of antioxidative enzymes in Oryza sativa: differential activation at different growth stages. Plant Sci. 2003;164(6):935–941.
  • An Y, Shen YB, Zhang ZX. Effects of mechanical damage and herbivore wounding on H2O2, metabolism and antioxidant enzyme activities in hybrid poplar leaves. J Forestry Res. 2009;20(2):156–160.
  • Thipyapong P, Hunt MD, Steffens JC. Systemic wound induction of potato (Solanum tuberosum) polyphenol oxidase. Phytochemistry. 1995;40(3):673–676.
  • Shah J, Zeier J. Long–distance communication and signal amplification in systemic acquired resistance. Front Plant Sci. 2013;4(4):30.
  • Dempsey DA, Klessig DF. SOS–too many signals for systemic acquired resistance? Trends Plant Sci. 2012;17(9):538–545.
  • Wind S, Beuerlein K, Eucker T, et al. Comparative pharmacology of chemically distinct NADPH oxidase inhibitors. Br J Pharmacol. 2010;161(4):885–898.
  • Santos NA, Bezerra CS, Martins NM, et al. Hydroxyl radical scavenger ameliorates cisplatin-induced nephrotoxicity by preventing oxidative stress, redox state unbalance, impairment of energetic metabolism and apoptosis in rat kidney mitochondria. Cancer Chemother Pharmacol. 2008;61(1):145–155.
  • Mittler R, Vanderauwera S, Suzuki N, et al. Ros signaling: the new wave? Trends Plant Sci. 2011;16(6):300–309.
  • Erb M, Flors V, Karlen D, et al. Signal signature of aboveground-induced resistance upon belowground herbivory in maize. Plant J. 2009;59(2):292–302.
  • Kaplan I, Halitschke R, Kessler A, et al. Physiological integration of roots and shoots in plant defense strategies links above and belowground herbivory. Ecol Lett. 2010;11(8):841–851.
  • Mhamdi A, Chaouch S, Van Breusegem F, et al. Catalase function in plants: a focus on Arabidopsis mutants as stress-mimic models. J Exp Bot. 2010;61(15):4197–4220.
  • Taggar GK, Gill RS, Gupta AK, et al. Fluctuations in peroxidase and catalase activities of resistant and susceptible black gram (vigna mungo (L) hepper) genotypes elicited by Bemisia tabaci (gennadius) feeding. Plant Signal Behav. 2012;7(10):1321–1329.
  • Cohen MF, Gurung S, Fukuto JM, et al. Controlled free radical attack in the apoplast: a hypothesis for roles of O, N and S species in regulatory and polysaccharide cleavage events during rapid abscission by Azolla. Plant Sci. 2014;217–218(1):120–126.
  • Heil M, Ton J. Long–distance signalling in plant defence. Trends Plant Sci. 2008;13(6):264–272.
  • Heil M. Damaged–self recognition in plant herbivore defence. Trends Plant Sci. 2009;14(7):356–363.
  • Heil M, Ibarra-Laclette E, Adame-Álvarez RM, et al. How plants sense wounds: damaged-self recognition is based on plant-derived elicitors and induces octadecanoid signaling. PLoS One. 2012;7(2):e30537.

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