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Divalent Cations Regulate the Ion Conductance Properties of Diverse Classes of Aquaporins

Aquaporins (AQPs) are known to facilitate water and solute fluxes across barrier membranes. An increasing number of AQPs are being found to serve as ion channels. Ion and water permeability of selected plant and animal AQPs (plant Arabidopsis thaliana AtPIP2;1, AtPIP2;2, AtPIP2;7, human Homo sapiens...

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Autores principales: Kourghi, Mohamad, Nourmohammadi, Saeed, Pei, Jinxin V., Qiu, Jiaen, McGaughey, Samantha, Tyerman, Stephen D., Byrt, Caitlin S., Yool, Andrea J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5713292/
https://www.ncbi.nlm.nih.gov/pubmed/29099773
http://dx.doi.org/10.3390/ijms18112323
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author Kourghi, Mohamad
Nourmohammadi, Saeed
Pei, Jinxin V.
Qiu, Jiaen
McGaughey, Samantha
Tyerman, Stephen D.
Byrt, Caitlin S.
Yool, Andrea J.
author_facet Kourghi, Mohamad
Nourmohammadi, Saeed
Pei, Jinxin V.
Qiu, Jiaen
McGaughey, Samantha
Tyerman, Stephen D.
Byrt, Caitlin S.
Yool, Andrea J.
author_sort Kourghi, Mohamad
collection PubMed
description Aquaporins (AQPs) are known to facilitate water and solute fluxes across barrier membranes. An increasing number of AQPs are being found to serve as ion channels. Ion and water permeability of selected plant and animal AQPs (plant Arabidopsis thaliana AtPIP2;1, AtPIP2;2, AtPIP2;7, human Homo sapiens HsAQP1, rat Rattus norvegicus RnAQP4, RnAQP5, and fly Drosophila melanogaster DmBIB) were expressed in Xenopus oocytes and examined in chelator-buffered salines to evaluate the effects of divalent cations (Ca(2+), Mg(2+), Ba(2+) and Cd(2+)) on ionic conductances. AtPIP2;1, AtPIP2;2, HsAQP1 and DmBIB expressing oocytes had ionic conductances, and showed differential sensitivity to block by external Ca(2+). The order of potency of inhibition by Ca(2+) was AtPIP2;2 > AtPIP2;1 > DmBIB > HsAQP1. Blockage of the AQP cation channels by Ba(2+) and Cd(2+) caused voltage-sensitive outward rectification. The channels with the highest sensitivity to Ca(2+) (AtPIP2;1 and AtPIP2;2) showed a distinctive relief of the Ca(2+) block by co-application of excess Ba(2+), suggesting that divalent ions act at the same site. Recognizing the regulatory role of divalent cations may enable the discovery of other classes of AQP ion channels, and facilitate the development of tools for modulating AQP ion channels. Modulators of AQPs have potential value for diverse applications including improving salinity tolerance in plants, controlling vector-borne diseases, and intervening in serious clinical conditions involving AQPs, such as cancer metastasis, cardiovascular or renal dysfunction.
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spelling pubmed-57132922017-12-07 Divalent Cations Regulate the Ion Conductance Properties of Diverse Classes of Aquaporins Kourghi, Mohamad Nourmohammadi, Saeed Pei, Jinxin V. Qiu, Jiaen McGaughey, Samantha Tyerman, Stephen D. Byrt, Caitlin S. Yool, Andrea J. Int J Mol Sci Article Aquaporins (AQPs) are known to facilitate water and solute fluxes across barrier membranes. An increasing number of AQPs are being found to serve as ion channels. Ion and water permeability of selected plant and animal AQPs (plant Arabidopsis thaliana AtPIP2;1, AtPIP2;2, AtPIP2;7, human Homo sapiens HsAQP1, rat Rattus norvegicus RnAQP4, RnAQP5, and fly Drosophila melanogaster DmBIB) were expressed in Xenopus oocytes and examined in chelator-buffered salines to evaluate the effects of divalent cations (Ca(2+), Mg(2+), Ba(2+) and Cd(2+)) on ionic conductances. AtPIP2;1, AtPIP2;2, HsAQP1 and DmBIB expressing oocytes had ionic conductances, and showed differential sensitivity to block by external Ca(2+). The order of potency of inhibition by Ca(2+) was AtPIP2;2 > AtPIP2;1 > DmBIB > HsAQP1. Blockage of the AQP cation channels by Ba(2+) and Cd(2+) caused voltage-sensitive outward rectification. The channels with the highest sensitivity to Ca(2+) (AtPIP2;1 and AtPIP2;2) showed a distinctive relief of the Ca(2+) block by co-application of excess Ba(2+), suggesting that divalent ions act at the same site. Recognizing the regulatory role of divalent cations may enable the discovery of other classes of AQP ion channels, and facilitate the development of tools for modulating AQP ion channels. Modulators of AQPs have potential value for diverse applications including improving salinity tolerance in plants, controlling vector-borne diseases, and intervening in serious clinical conditions involving AQPs, such as cancer metastasis, cardiovascular or renal dysfunction. MDPI 2017-11-03 /pmc/articles/PMC5713292/ /pubmed/29099773 http://dx.doi.org/10.3390/ijms18112323 Text en © 2017 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/).
spellingShingle Article
Kourghi, Mohamad
Nourmohammadi, Saeed
Pei, Jinxin V.
Qiu, Jiaen
McGaughey, Samantha
Tyerman, Stephen D.
Byrt, Caitlin S.
Yool, Andrea J.
Divalent Cations Regulate the Ion Conductance Properties of Diverse Classes of Aquaporins
title Divalent Cations Regulate the Ion Conductance Properties of Diverse Classes of Aquaporins
title_full Divalent Cations Regulate the Ion Conductance Properties of Diverse Classes of Aquaporins
title_fullStr Divalent Cations Regulate the Ion Conductance Properties of Diverse Classes of Aquaporins
title_full_unstemmed Divalent Cations Regulate the Ion Conductance Properties of Diverse Classes of Aquaporins
title_short Divalent Cations Regulate the Ion Conductance Properties of Diverse Classes of Aquaporins
title_sort divalent cations regulate the ion conductance properties of diverse classes of aquaporins
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5713292/
https://www.ncbi.nlm.nih.gov/pubmed/29099773
http://dx.doi.org/10.3390/ijms18112323
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