Extracellular ATP

Living organisms acquire or synthesize high energy molecules, which they frugally conserve and use to meet their cellular metabolic demands. Therefore, it is surprising that ATP, the most accessible and commonly utilized chemical energy carrier, is actively secreted to the extracellular matrix of cells. It is now becoming clear that in plants this extracellular ATP (eATP) is not wasted, but harnessed at the cell surface to signal across the plasma membrane of the secreting cell and neighboring cells to control gene expression and influence plant development. Identification of the gene/protein networks regulated by eATP-mediated signaling should provide insight into the physiological roles of eATP in plants. By disrupting eATP-mediated signaling, we have identified pathogen defense genes as part of the eATP-regulated gene circuitry, leading us to the discovery that eATP is a negative regulator of pathogen defense in plants.1 Previously, we reported that eATP is a key signal molecule that modulates programmed cell death in plants.2 A complex picture is now emerging, in which eATP-mediated signaling cross-talks with signaling mediated by the major plant defense hormone, salicylic acid, in the regulation of pathogen defense and cell death.

[1]  K. Lindsey,et al.  Extracellular ATP is a regulator of pathogen defence in plants. , 2009, The Plant journal : for cell and molecular biology.

[2]  Seiko F. Okada,et al.  Touch induces ATP release in Arabidopsis roots that is modulated by the heterotrimeric G‐protein complex , 2009, FEBS letters.

[3]  Sun-Hee Kim,et al.  Hypertonic Stress Increased Extracellular ATP Levels and the Expression of Stress-Responsive Genes in Arabidopsis thaliana Seedlings , 2009, Bioscience, biotechnology, and biochemistry.

[4]  J. Davies,et al.  Plant extracellular ATP signalling by plasma membrane NADPH oxidase and Ca2+ channels. , 2009, The Plant journal : for cell and molecular biology.

[5]  Shu-jing Wu,et al.  Extracellular ATP-induced NO production and its dependence on membrane Ca2+ flux in Salvia miltiorrhiza hairy roots , 2008, Journal of experimental botany.

[6]  Shu-jing Wu,et al.  The signaling role of extracellular ATP and its dependence on Ca2+ flux in elicitation of Salvia miltiorrhiza hairy root cultures. , 2008, Plant & cell physiology.

[7]  C. Casalongué,et al.  Extracellular ATP Induces Nitric Oxide Production in Tomato Cell Suspensions1 , 2007, Plant Physiology.

[8]  N. Dale,et al.  Purine-mediated signalling triggers eye development , 2007, Nature.

[9]  D. Arnold,et al.  Apyrases (Nucleoside Triphosphate-Diphosphohydrolases) Play a Key Role in Growth Control in Arabidopsis1[W][OA] , 2007, Plant Physiology.

[10]  G. Stacey,et al.  Extracellular ATP in Plants. Visualization, Localization, and Analysis of Physiological Significance in Growth and Signaling1[W] , 2006, Plant Physiology.

[11]  Elena P Ivanova,et al.  ATP level variations in heterotrophic bacteria during attachment on hydrophilic and hydrophobic surfaces. , 2006, International microbiology : the official journal of the Spanish Society for Microbiology.

[12]  Stephen C. Stout,et al.  Extracellular ATP Induces the Accumulation of Superoxide via NADPH Oxidases in Arabidopsis1 , 2006, Plant Physiology.

[13]  N. Yao,et al.  Arabidopsis ACCELERATED CELL DEATH2 Modulates Programmed Cell Death[W] , 2005, The Plant Cell Online.

[14]  K. Lindsey,et al.  Extracellular ATP Functions as an Endogenous External Metabolite Regulating Plant Cell Viability , 2005, The Plant Cell Online.

[15]  J. Davies,et al.  Is ATP a signalling agent in plants , 2005 .

[16]  Elizabeth Hénaff,et al.  Evidence of a Novel Cell Signaling Role for Extracellular Adenosine Triphosphates and Diphosphates in Arabidopsis , 2004, The Plant Cell Online.

[17]  Martin J. Mueller,et al.  Light conditions influence specific defence responses in incompatible plant–pathogen interactions: uncoupling systemic resistance from salicylic acid and PR-1 accumulation , 2004, Planta.

[18]  M. Roca,et al.  Chlorophyll breakdown: Pheophorbide a oxygenase is a Rieske-type iron–sulfur protein, encoded by the accelerated cell death 1 gene , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[19]  J. Davies,et al.  Is ATP a Signaling Agent in Plants?1 , 2003, Plant Physiology.

[20]  J. Greenberg,et al.  The Arabidopsis-accelerated cell death gene ACD2 encodes red chlorophyll catabolite reductase and suppresses the spread of disease symptoms. , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[21]  Collin Thomas,et al.  A Role for Ectophosphatase in Xenobiotic Resistance , 2000, Plant Cell.

[22]  S. Briggs,et al.  A Porphyrin Pathway Impairment Is Responsible for the Phenotype of a Dominant Disease Lesion Mimic Mutant of Maize , 1998, Plant Cell.

[23]  P. Saindrenan,et al.  Spatial and Temporal Induction of Cell Death, Defense Genes, and Accumulation of Salicylic Acid in Tobacco Leaves Reacting Hypersensitively to a Fungal Glycoprotein Elicitor , 1997 .

[24]  D F Klessig,et al.  Salicylic Acid: A Likely Endogenous Signal in the Resistance Response of Tobacco to Viral Infection , 1990, Science.

[25]  R. Parish,et al.  Extracellular ATP, ecto‐ATPase and calcium influx in Dictyostelium discoideum cells , 1980, FEBS letters.

[26]  P. Holton The liberation of adenosine triphosphate on antidromic stimulation of sensory nerves , 1959, The Journal of physiology.