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      The Relationship between Turgor Pressure Change and Cell Hydraulics of Midrib Parenchyma Cells in the Leaves of Zea mays

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          Abstract

          Leaf dehydration decreases water potential and cell turgor pressure. Therefore, changes in cell turgor pressure may regulate water transport across plant cell membranes. Using a cell pressure probe, the hydraulic properties of parenchyma cells in the midrib of maize ( Zea mays L.) leaves were measured (half time T 1 / 2 of water exchange in cells as a measure of hydraulic conductivity Lp). Using intact plants with root systems encased in a pressure chamber, the root systems were pressurized and the turgor pressure in leaf cells increased by increments up to 0.3 MPa. However, the increase in the cell turgor did not increase but stabilized T 1 / 2 values. Increased water potential in leaf cells seemed to have stabilizing effects on the T 1 / 2 probably due to enhanced water availability. When the cell turgor decreased by 0.1 MPa to 0.3 MPa with releasing the pressure in the pressure chamber, T 1 / 2 was temporarily increased to a large degree, a factor of up to 13 within 30 min.

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          Most cited references33

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          Aquaporins in Plants.

          Aquaporins are membrane channels that facilitate the transport of water and small neutral molecules across biological membranes of most living organisms. In plants, aquaporins occur as multiple isoforms reflecting a high diversity of cellular localizations, transport selectivity, and regulation properties. Plant aquaporins are localized in the plasma membrane, endoplasmic reticulum, vacuoles, plastids and, in some species, in membrane compartments interacting with symbiotic organisms. Plant aquaporins can transport various physiological substrates in addition to water. Of particular relevance for plants is the transport of dissolved gases such as carbon dioxide and ammonia or metalloids such as boron and silicon. Structure-function studies are developed to address the molecular and cellular mechanisms of plant aquaporin gating and subcellular trafficking. Phosphorylation plays a central role in these two processes. These mechanisms allow aquaporin regulation in response to signaling intermediates such as cytosolic pH and calcium, and reactive oxygen species. Combined genetic and physiological approaches are now integrating this knowledge, showing that aquaporins play key roles in hydraulic regulation in roots and leaves, during drought but also in response to stimuli as diverse as flooding, nutrient availability, temperature, or light. A general hydraulic control of plant tissue expansion by aquaporins is emerging, and their role in key developmental processes (seed germination, emergence of lateral roots) has been established. Plants with genetically altered aquaporin functions are now tested for their ability to improve plant tolerance to stresses. In conclusion, research on aquaporins delineates ever expanding fields in plant integrative biology thereby establishing their crucial role in plants.
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            Aquaporins: highly regulated channels controlling plant water relations.

            Plant growth and development are dependent on tight regulation of water movement. Water diffusion across cell membranes is facilitated by aquaporins that provide plants with the means to rapidly and reversibly modify water permeability. This is done by changing aquaporin density and activity in the membrane, including posttranslational modifications and protein interaction that act on their trafficking and gating. At the whole organ level aquaporins modify water conductance and gradients at key "gatekeeper" cell layers that impact on whole plant water flow and plant water potential. In this way they may act in concert with stomatal regulation to determine the degree of isohydry/anisohydry. Molecular, physiological, and biophysical approaches have demonstrated that variations in root and leaf hydraulic conductivity can be accounted for by aquaporins but this must be integrated with anatomical considerations. This Update integrates these data and emphasizes the central role played by aquaporins in regulating plant water relations.
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              Leaf hydraulics.

              Leaves are extraordinarily variable in form, longevity, venation architecture, and capacity for photosynthetic gas exchange. Much of this diversity is linked with water transport capacity. The pathways through the leaf constitute a substantial (>or=30%) part of the resistance to water flow through plants, and thus influence rates of transpiration and photosynthesis. Leaf hydraulic conductance (K(leaf)) varies more than 65-fold across species, reflecting differences in the anatomy of the petiole and the venation architecture, as well as pathways beyond the xylem through living tissues to sites of evaporation. K(leaf) is highly dynamic over a range of time scales, showing circadian and developmental trajectories, and responds rapidly, often reversibly, to changes in temperature, irradiance, and water supply. This review addresses how leaf structure and physiology influence K(leaf), and the mechanisms by which K(leaf) contributes to dynamic functional responses at the level of both individual leaves and the whole plant.
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                Author and article information

                Journal
                Cells
                Cells
                cells
                Cells
                MDPI
                2073-4409
                22 October 2018
                October 2018
                : 7
                : 10
                : 180
                Affiliations
                [1 ]Department of Plant Ecology, Bayreuth University, D-95440 Bayreuth, Germany; yangmink@ 123456korea.kr (Y.X.K.); burkhard.stumpf@ 123456uni-bayreuth.de (B.S.)
                [2 ]Division of Soil and Fertilizer, National Institute of Agricultural Sciences, RDA, Wanju 55365, Jeollabuk-do, Korea
                [3 ]Department of Mechanical Engineering, Pohang University of Science and Technology (POSTECH), Pohang 37673, Gyeongbuk, Korea
                Author notes
                [* ]Correspondence: jksung@ 123456korea.kr (J.S.); sjlee@ 123456postech.ac.kr (S.J.L.); Tel.: +82-63-238-2445 or +82-63-238-2822 (J.S.); +82-54-279-2169 or +82-54-279-3199 (S.J.L.)
                [†]

                Current address: Division of Soil and Fertilizer, National Institute of Agricultural Sciences, RDA, Wanju 55365, Jeollabuk-do, Korea.

                Article
                cells-07-00180
                10.3390/cells7100180
                6210020
                30360453
                7f26fc94-a4ed-42f5-9dce-86a534809470
                © 2018 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 17 September 2018
                : 18 October 2018
                Categories
                Article

                aquaporin,cell pressure probe,hydraulic conductivity,zea mays l.

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