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Remodelling of lace plant leaves: antioxidants and ROS are key regulators of programmed cell death

Antioxidants and reactive oxygen species are integral for programmed cell death signaling during perforation formation in the lace plant ( Aponogeton madagascariensis ). The lace plant is an excellent model system for studying developmentally regulated programmed cell death (PCD). During early lace...

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Autores principales: Dauphinee, Adrian N., Fletcher, Jacob I., Denbigh, Georgia L., Lacroix, Christian R., Gunawardena, Arunika H. L. A. N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5486552/
https://www.ncbi.nlm.nih.gov/pubmed/28389868
http://dx.doi.org/10.1007/s00425-017-2683-y
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author Dauphinee, Adrian N.
Fletcher, Jacob I.
Denbigh, Georgia L.
Lacroix, Christian R.
Gunawardena, Arunika H. L. A. N.
author_facet Dauphinee, Adrian N.
Fletcher, Jacob I.
Denbigh, Georgia L.
Lacroix, Christian R.
Gunawardena, Arunika H. L. A. N.
author_sort Dauphinee, Adrian N.
collection PubMed
description Antioxidants and reactive oxygen species are integral for programmed cell death signaling during perforation formation in the lace plant ( Aponogeton madagascariensis ). The lace plant is an excellent model system for studying developmentally regulated programmed cell death (PCD). During early lace plant leaf development, PCD systematically deletes cells resulting in a perforated leaf morphology that is unique in planta. A distinct feature in young lace plant leaves is an abundance of anthocyanins, which have antioxidant properties. The first sign of PCD induction is the loss of anthocyanin pigmentation in cells that are targeted for destruction, which results in a visible gradient of cell death. The cellular dynamics and time course of lace plant PCD are well documented; however, the signals involved in the pathway remain elusive. This study investigates the roles of antioxidants and ROS in developmental PCD signaling during lace plant perforation formation. The involvement of antioxidants and ROS in the pathway was determined using a variety of techniques including pharmacological whole plant experimentation, long-term live cell imaging, the 2,2′-azino-bis-3-ethylbenzothiazoline-6-sulfonic acid anti-radical activity assay, and western blot analysis. Results indicate that antioxidants and ROS are key regulators of PCD during the remodelling of lace plant leaves. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00425-017-2683-y) contains supplementary material, which is available to authorized users.
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spelling pubmed-54865522017-07-17 Remodelling of lace plant leaves: antioxidants and ROS are key regulators of programmed cell death Dauphinee, Adrian N. Fletcher, Jacob I. Denbigh, Georgia L. Lacroix, Christian R. Gunawardena, Arunika H. L. A. N. Planta Original Article Antioxidants and reactive oxygen species are integral for programmed cell death signaling during perforation formation in the lace plant ( Aponogeton madagascariensis ). The lace plant is an excellent model system for studying developmentally regulated programmed cell death (PCD). During early lace plant leaf development, PCD systematically deletes cells resulting in a perforated leaf morphology that is unique in planta. A distinct feature in young lace plant leaves is an abundance of anthocyanins, which have antioxidant properties. The first sign of PCD induction is the loss of anthocyanin pigmentation in cells that are targeted for destruction, which results in a visible gradient of cell death. The cellular dynamics and time course of lace plant PCD are well documented; however, the signals involved in the pathway remain elusive. This study investigates the roles of antioxidants and ROS in developmental PCD signaling during lace plant perforation formation. The involvement of antioxidants and ROS in the pathway was determined using a variety of techniques including pharmacological whole plant experimentation, long-term live cell imaging, the 2,2′-azino-bis-3-ethylbenzothiazoline-6-sulfonic acid anti-radical activity assay, and western blot analysis. Results indicate that antioxidants and ROS are key regulators of PCD during the remodelling of lace plant leaves. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00425-017-2683-y) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2017-04-07 2017 /pmc/articles/PMC5486552/ /pubmed/28389868 http://dx.doi.org/10.1007/s00425-017-2683-y Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Article
Dauphinee, Adrian N.
Fletcher, Jacob I.
Denbigh, Georgia L.
Lacroix, Christian R.
Gunawardena, Arunika H. L. A. N.
Remodelling of lace plant leaves: antioxidants and ROS are key regulators of programmed cell death
title Remodelling of lace plant leaves: antioxidants and ROS are key regulators of programmed cell death
title_full Remodelling of lace plant leaves: antioxidants and ROS are key regulators of programmed cell death
title_fullStr Remodelling of lace plant leaves: antioxidants and ROS are key regulators of programmed cell death
title_full_unstemmed Remodelling of lace plant leaves: antioxidants and ROS are key regulators of programmed cell death
title_short Remodelling of lace plant leaves: antioxidants and ROS are key regulators of programmed cell death
title_sort remodelling of lace plant leaves: antioxidants and ros are key regulators of programmed cell death
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5486552/
https://www.ncbi.nlm.nih.gov/pubmed/28389868
http://dx.doi.org/10.1007/s00425-017-2683-y
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