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      Hydrogen Peroxide Signaling in Plant Development and Abiotic Responses: Crosstalk with Nitric Oxide and Calcium

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          Abstract

          Hydrogen peroxide (H 2O 2), as a reactive oxygen species, is widely generated in many biological systems. It has been considered as an important signaling molecule that mediates various physiological and biochemical processes in plants. Normal metabolism in plant cells results in H 2O 2 generation, from a variety of sources. Also, it is now clear that nitric oxide (NO) and calcium (Ca 2+) function as signaling molecules in plants. Both H 2O 2 and NO are involved in plant development and abiotic responses. A wide range of evidences suggest that NO could be generated under similar stress conditions and with similar kinetics as H 2O 2. The interplay between H 2O 2 and NO has important functional implications to modulate transduction processes in plants. Moreover, close interaction also exists between H 2O 2 and Ca 2+ in response to development and abiotic stresses in plants. Cellular responses to H 2O 2 and Ca 2+ signaling systems are complex. There is quite a bit of interaction between H 2O 2 and Ca 2+ signaling in responses to several stimuli. This review aims to introduce these evidences in our understanding of the crosstalk among H 2O 2, NO, and Ca 2+ signaling which regulates plant growth and development, and other cellular and physiological responses to abiotic stresses.

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          Most cited references115

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          Redox sensing and signalling associated with reactive oxygen in chloroplasts, peroxisomes and mitochondria

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            Dual action of the active oxygen species during plant stress responses.

            Adaptation to environmental changes is crucial for plant growth and survival. However, the molecular and biochemical mechanisms of adaptation are still poorly understood and the signaling pathways involved remain elusive. Active oxygen species (AOS) have been proposed as a central component of plant adaptation to both biotic and abiotic stresses. Under such conditions, AOS may play two very different roles: exacerbating damage or signaling the activation of defense responses. Such a dual function was first described in pathogenesis but has also recently been demonstrated during several abiotic stress responses. To allow for these different roles, cellular levels of AOS must be tightly controlled. The numerous AOS sources and a complex system of oxidant scavengers provide the flexibility necessary for these functions. This review discusses the dual action of AOS during plant stress responses.
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              Role of nitric oxide synthesis in macrophage antimicrobial activity.

              Research over the past 5 years has demonstrated that immunologic activation of mouse macrophages induces the activity of nitric oxide synthase, which oxidizes a guanidino nitrogen of L-arginine, yielding citrulline and the reactive radical, nitric oxide. A review of the biochemistry and immunologic regulation of this pathway in macrophages provides a backdrop against which to evaluate its effector functions. Reports published in the past 2 years suggest that synthesis of NO mediates much of the antimicrobial activity of mouse macrophages against some fungal, helminthic, protozoal and bacterial pathogens.
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                Author and article information

                Contributors
                Journal
                Front Plant Sci
                Front Plant Sci
                Front. Plant Sci.
                Frontiers in Plant Science
                Frontiers Media S.A.
                1664-462X
                04 March 2016
                2016
                : 7
                : 230
                Affiliations
                Department of Ornamental Horticulture, College of Horticulture, Gansu Agricultural University Lanzhou, China
                Author notes

                Edited by: Cristina Ortega-Villasante, Universidad Autónoma de Madrid, Spain

                Reviewed by: Eva-Mari Aro, University of Turku, Finland; Clay Carter, University of Minnesota Twin Cities, USA

                *Correspondence: Weibiao Liao liaowb@ 123456gsau.edu.cn

                This article was submitted to Plant Physiology, a section of the journal Frontiers in Plant Science

                Article
                10.3389/fpls.2016.00230
                4777889
                26973673
                3679bbb4-c2af-4a5c-8c7d-281c104740d4
                Copyright © 2016 Niu and Liao.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 14 November 2015
                : 11 February 2016
                Page count
                Figures: 3, Tables: 6, Equations: 0, References: 127, Pages: 14, Words: 11075
                Funding
                Funded by: National Natural Science Foundation of China 10.13039/501100001809
                Award ID: 31160398
                Award ID: 31560563
                Categories
                Plant Science
                Review

                Plant science & Botany
                hydrogen peroxide (h2o2),nitric oxide (no),calcium (ca2+),signal molecule,crosstalk

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