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      Calcium Efflux Systems in Stress Signaling and Adaptation in Plants

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          Abstract

          Transient cytosolic calcium ([Ca 2+] cyt) elevation is an ubiquitous denominator of the signaling network when plants are exposed to literally every known abiotic and biotic stress. These stress-induced [Ca 2+] cyt elevations vary in magnitude, frequency, and shape, depending on the severity of the stress as well the type of stress experienced. This creates a unique stress-specific calcium “signature” that is then decoded by signal transduction networks. While most published papers have been focused predominantly on the role of Ca 2+ influx mechanisms to shaping [Ca 2+] cyt signatures, restoration of the basal [Ca 2+] cyt levels is impossible without both cytosolic Ca 2+ buffering and efficient Ca 2+ efflux mechanisms removing excess Ca 2+ from cytosol, to reload Ca 2+ stores and to terminate Ca 2+ signaling. This is the topic of the current review. The molecular identity of two major types of Ca 2+ efflux systems, Ca 2+-ATPase pumps and Ca 2+/H + exchangers, is described, and their regulatory modes are analyzed in detail. The spatial and temporal organization of calcium signaling networks is described, and the importance of existence of intracellular calcium microdomains is discussed. Experimental evidence for the role of Ca 2+ efflux systems in plant responses to a range of abiotic and biotic factors is summarized. Contribution of Ca 2+-ATPase pumps and Ca 2+/H + exchangers in shaping [Ca 2+] cyt signatures is then modeled by using a four-component model (plasma- and endo-membrane-based Ca 2+-permeable channels and efflux systems) taking into account the cytosolic Ca 2+ buffering. It is concluded that physiologically relevant variations in the activity of Ca 2+-ATPase pumps and Ca 2+/H + exchangers are sufficient to fully describe all the reported experimental evidence and determine the shape of [Ca 2+] cyt signatures in response to environmental stimuli, emphasizing the crucial role these active efflux systems play in plant adaptive responses to environment.

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          Most cited references178

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          Reactive oxygen species produced by NADPH oxidase regulate plant cell growth.

          Cell expansion is a central process in plant morphogenesis, and the elongation of roots and root hairs is essential for uptake of minerals and water from the soil. Ca2+ influx from the extracellular store is required for (and sets the rates of) cell elongation in roots. Arabidopsis thaliana rhd2 mutants are defective in Ca2+ uptake and consequently cell expansion is compromised--rhd2 mutants have short root hairs and stunted roots. To determine the regulation of Ca2+ acquisition in growing root cells we show here that RHD2 is an NADPH oxidase, a protein that transfers electrons from NADPH to an electron acceptor leading to the formation of reactive oxygen species (ROS). We show that ROS accumulate in growing wild-type (WT) root hairs but their levels are markedly decreased in rhd2 mutants. Blocking the activity of the NADPH oxidase with diphenylene iodonium (DPI) inhibits ROS formation and phenocopies Rhd2-. Treatment of rhd2 roots with ROS partly suppresses the mutant phenotype and stimulates the activity of plasma membrane hyperpolarization-activated Ca2+ channels, the predominant root Ca2+ acquisition system. This indicates that NADPH oxidases control development by making ROS that regulate plant cell expansion through the activation of Ca2+ channels.
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            Calcium channels activated by hydrogen peroxide mediate abscisic acid signalling in guard cells.

            Drought is a major threat to agricultural production. Plants synthesize the hormone abscisic acid (ABA) in response to drought, triggering a signalling cascade in guard cells that results in stomatal closure, thus reducing water loss. ABA triggers an increase in cytosolic calcium in guard cells ([Ca2+]cyt) that has been proposed to include Ca2+ influx across the plasma membrane. However, direct recordings of Ca2+ currents have been limited and the upstream activation mechanisms of plasma membrane Ca2+ channels remain unknown. Here we report activation of Ca2+-permeable channels in the plasma membrane of Arabidopsis guard cells by hydrogen peroxide. The H2O2-activated Ca2+ channels mediate both influx of Ca2+ in protoplasts and increases in [Ca2+]cyt in intact guard cells. ABA induces the production of H2O2 in guard cells. If H2O2 production is blocked, ABA-induced closure of stomata is inhibited. Moreover, activation of Ca2+ channels by H2O2 and ABA- and H2O2-induced stomatal closing are disrupted in the recessive ABA-insensitive mutant gca2. These data indicate that ABA-induced H2O2 production and the H2O2-activated Ca2+ channels are important mechanisms for ABA-induced stomatal closing.
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              Calcium in plants.

              Calcium is an essential plant nutrient. It is required for various structural roles in the cell wall and membranes, it is a counter-cation for inorganic and organic anions in the vacuole, and the cytosolic Ca2+ concentration ([Ca2+]cyt) is an obligate intracellular messenger coordinating responses to numerous developmental cues and environmental challenges. This article provides an overview of the nutritional requirements of different plants for Ca, and how this impacts on natural flora and the Ca content of crops. It also reviews recent work on (a) the mechanisms of Ca2+ transport across cellular membranes, (b) understanding the origins and specificity of [Ca2+]cyt signals and (c) characterizing the cellular [Ca2+]cyt-sensors (such as calmodulin, calcineurin B-like proteins and calcium-dependent protein kinases) that allow plant cells to respond appropriately to [Ca2+]cyt signals.
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                Author and article information

                Journal
                Front Plant Sci
                Front Plant Sci
                Front. Plant Sci.
                Frontiers in plant science
                Frontiers Research Foundation
                1664-462X
                15 September 2011
                02 December 2011
                2011
                : 2
                : 85
                Affiliations
                [1] 1simpleSchool of Agricultural Science, University of Tasmania Hobart, TAS, Australia
                [2] 2simpleCentro Universitario de Investigaciones Biomédicas, Universidad de Colima Colima, México
                [3] 3simpleSchool of Mathematics and Physics, University of Tasmania Hobart, TAS, Australia
                [4] 4simpleDepartment of Plant Biology, University of Copenhagen Copenhagen, Denmark
                Author notes

                Edited by: Abraham D. Stroock, Cornell University, USA

                Reviewed by: Jinkee Lee, Brown University, USA; Barbara G. Pickard, Washington University in St. Louis, USA

                *Correspondence: Sergey Shabala, School of Agricultural Science, University of Tasmania, Private Bag 54, Hobart, TAS 7001, Australia. e-mail: sergey.shabala@ 123456utas.edu.au

                This article was submitted to Frontiers in Plant Biophysics and Modeling, a specialty of Frontiers in Plant Science.

                Article
                10.3389/fpls.2011.00085
                3355617
                22639615
                755872c3-a141-40ef-a9e8-8a59fd64e220
                Copyright © 2011 Bose, Pottosin, Shabala, Palmgren and Shabala.

                This is an open-access article subject to a non-exclusive license between the authors and Frontiers Media SA, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and other Frontiers conditions are complied with.

                History
                : 15 August 2011
                : 04 November 2011
                Page count
                Figures: 7, Tables: 1, Equations: 3, References: 190, Pages: 17, Words: 15827
                Categories
                Plant Science
                Review Article

                Plant science & Botany
                signatures,ca2+-atpase,calcium exchanger,oscillations,cytosolic calcium
                Plant science & Botany
                signatures, ca2+-atpase, calcium exchanger, oscillations, cytosolic calcium

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