Extracellular ATP: an unexpected role as a signaler in plants

Trends in Plant Science

Volumn 12, Issue 11, 2007, Pages 522-527

  Roux, Stanley J ^a   Steinebrunner, Iris ^b  

^a UNIVERSITY OF TEXAS AT AUSTIN   (United States)

^b DRESDEN UNIVERSITY OF TECHNOLOGY   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATE; CALCIUM; PURINERGIC RECEPTOR;

CELL MEMBRANE; METABOLISM; PHYSIOLOGY; PLANT PHYSIOLOGY; PLANT ROOT; REVIEW; SIGNAL TRANSDUCTION;

ADENOSINE TRIPHOSPHATE; CALCIUM; CELL MEMBRANE; PLANT PHYSIOLOGY; PLANT ROOTS; RECEPTORS, PURINERGIC; SIGNAL TRANSDUCTION;

ANIMALIA;

EID: 35548964674     PISSN: 13601385     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tplants.2007.09.003     Document Type: Review

References (32)

1. Burnstock G., and Knight G.E. Cellular distribution and functions of P2 receptor subtypes in different systems. Int. Rev. Cytol. 240 (2004) 31-51
2. Lew R.R., and Dearnaley J.D.W. Extracellular nucleotide effects on the electrical properties of growing Arabidopsis thaliana root hairs. Plant Sci. 153 (2000) 1-6
3. Demidchik V., et al. Is ATP a signaling agent in plants?. Plant Physiol. 133 (2003) 456-461
4. Gout E., et al. Regulation of intracellular pH values in higher plants. Carbon-13 and phosphorus-31 nuclear magnetic resonance studies. J. Biol. Chem. 267 (1992) 13903-13909
5. Song C.J., et al. Extracellular ATP induces the accumulation of superoxide via NADPH oxidases in Arabidopsis. Plant Physiol. 140 (2006) 1222-1232
6. Yegutkin G.G., et al. The detection of micromolar pericellular ATP pool on lymphocyte surface by using lymphoid ecto-adenylate kinase as intrinsic ATP sensor. Mol. Biol. Cell 17 (2006) 3378-3385
7. Zimmermann H. Extracellular metabolism of ATP and other nucleotides. Naunyn Schmiedebergs Arch. Pharmacol. 362 (2000) 299-309
8. Abraham E.H., et al. The multidrug resistance (mdr1) gene-product functions as an ATP channel. Proc. Natl. Acad. Sci. U. S. A. 90 (1993) 312-316
9. Thomas C., et al. A role for ectophosphatase in xenobiotic resistance. Plant Cell 12 (2000) 519-533
10. 2+ waves are propagated via ATP release and purinergic receptor activation. Am. J. Physiol. Cell Physiol. 279 (2000) C295-C307
11. Jeter C.R., et al. Evidence of a novel cell signaling role for extracellular adenosine triphosphates and diphosphates in Arabidopsis. Plant Cell 16 (2004) 2652-2664
12. Lazarowski E.R., et al. Mechanisms of release of nucleotides and integration of their action as P2X- and P2Y-receptor activating molecules. Mol. Pharmacol. 64 (2003) 785-795
13. Kim S.Y., et al. Extracellular ATP in plants. Visualization, localization, and analysis of physiological significance in growth and signaling. Plant Physiol. 142 (2006) 984-992
14. Wu J., et al. Apyrases (nucleoside triphosphate-diphosphohydrolases) play key role in growth control in Arabidopsis. Plant Physiol. 144 (2007) 961-975
15. Jeter C., and Roux S.J. Plant responses to extracellular nucleotides: Cellular processes and biological effects. Purinergic Signal. 2 (2006) 443-449
16. Sagi M., et al. Plant respiratory burst oxidase homologs impinge on wound responsiveness and development in Lycopersicon esculentum. Plant Cell 16 (2004) 616-628
17. Bours M.J.L., et al. Adenosine 5′-triphosphate and adenosine as endogenous signaling molecules in immunity and inflammation. Pharmacol. Ther. 112 (2006) 358-404
18. Steinebrunner I., et al. Molecular and biochemical comparison of two different apyrases from Arabidopsis thaliana. Plant Physiol. Biochem. 38 (2000) 913-922
19. Thomas C., et al. Apyrase functions in plant phosphate nutrition and mobilizes phosphate from extracellular ATP. Plant Physiol. 119 (1999) 543-551
20. Steinebrunner I., et al. Disruption of apyrases inhibits pollen germination in Arabidopsis. Plant Physiol. 131 (2003) 1638-1647
21. Wolf C., et al. Developmental defects and seedling lethality in apyrase AtAPY1 and AtAPY2 double knockout mutants. Plant Mol. Biol. 64 (2007) 657-672
22. McAlvin C.B., and Stacey G. Transgenic expression of the soybean apyrase in Lotus japonicus enhances nodulation. Plant Physiol. 137 (2005) 1456-1462
23. Chivasa S., et al. Extracellular ATP functions as an endogenous external metabolite regulating plant cell viability. Plant Cell 17 (2005) 3019-3034
24. Roux S.J., et al. Regulation of plant growth and development by extracellular nucleotides. In: Baluska F., et al. (Ed). Communication in Plants (2006), Springer 221-234
25. Geisler M., and Murphy A.S. The ABC of auxin transport: the role of p-glycoproteins in plant development. FEBS Lett. 580 (2006) 1094-1102
26. Tang W.Q., et al. Extracellular ATP inhibits root gravitropism at concentrations that inhibit polar auxin transport. Plant Physiol. 131 (2003) 147-154
27. Koshimizu T., et al. Contributions of the C-terminal domain to the control of P2X receptor desensitization. J. Biol. Chem. 274 (1999) 37651-37657
28. Nejidat A., et al. Stomatal response to ATP mediated by phytochrome. Physiol. Plant. 57 (1983) 367-370
29. Kamizyo A., and Tanaka N. Studies on the generative nuclear division. III. Effect of exogenous ATP on the generative nuclear division in Lilium longiflorum. Cytologia (Tokyo) 47 (1982) 195-205
30. Williamson R.E. Cytoplasmic streaming in chara: a cell model activated by ATP and inhibited by cytochalasin B. J. Cell Sci. 17 (1975) 655-668
31. Jaffe M.J. The role of ATP in mechanically stimulated rapid closure of the Venus's flytrap. Plant Physiol. 51 (1973) 17-18
32. Udvardy J., and Farkas G.L. ATP stimulates the formation of nucleases in excised Avena leaves. Zeitschrift für Pflanzenphysiologie 69 (1973) 399-401