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Male–female communication triggers calcium signatures during fertilization in Arabidopsis

Cell–cell communication and interaction is critical during fertilization and triggers free cytosolic calcium ([Ca(2+)](cyto)) as a key signal for egg activation and a polyspermy block in animal oocytes. Fertilization in flowering plants is more complex, involving interaction of a pollen tube with eg...

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Autores principales: Denninger, Philipp, Bleckmann, Andrea, Lausser, Andreas, Vogler, Frank, Ott, Thomas, Ehrhardt, David W., Frommer, Wolf B., Sprunck, Stefanie, Dresselhaus, Thomas, Grossmann, Guido
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Pub. Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4143946/
https://www.ncbi.nlm.nih.gov/pubmed/25145880
http://dx.doi.org/10.1038/ncomms5645
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author Denninger, Philipp
Bleckmann, Andrea
Lausser, Andreas
Vogler, Frank
Ott, Thomas
Ehrhardt, David W.
Frommer, Wolf B.
Sprunck, Stefanie
Dresselhaus, Thomas
Grossmann, Guido
author_facet Denninger, Philipp
Bleckmann, Andrea
Lausser, Andreas
Vogler, Frank
Ott, Thomas
Ehrhardt, David W.
Frommer, Wolf B.
Sprunck, Stefanie
Dresselhaus, Thomas
Grossmann, Guido
author_sort Denninger, Philipp
collection PubMed
description Cell–cell communication and interaction is critical during fertilization and triggers free cytosolic calcium ([Ca(2+)](cyto)) as a key signal for egg activation and a polyspermy block in animal oocytes. Fertilization in flowering plants is more complex, involving interaction of a pollen tube with egg adjoining synergid cells, culminating in release of two sperm cells and their fusion with the egg and central cell, respectively. Here, we report the occurrence and role of [Ca(2+)](cyto) signals during the entire double fertilization process in Arabidopsis. [Ca(2+)](cyto) oscillations are initiated in synergid cells after physical contact with the pollen tube apex. In egg and central cells, a short [Ca(2+)](cyto) transient is associated with pollen tube burst and sperm cell arrival. A second extended [Ca(2+)](cyto) transient solely in the egg cell is correlated with successful fertilization. Thus, each female cell type involved in double fertilization displays a characteristic [Ca(2+)](cyto) signature differing by timing and behaviour from [Ca(2+)](cyto) waves reported in mammals.
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spelling pubmed-41439462014-09-03 Male–female communication triggers calcium signatures during fertilization in Arabidopsis Denninger, Philipp Bleckmann, Andrea Lausser, Andreas Vogler, Frank Ott, Thomas Ehrhardt, David W. Frommer, Wolf B. Sprunck, Stefanie Dresselhaus, Thomas Grossmann, Guido Nat Commun Article Cell–cell communication and interaction is critical during fertilization and triggers free cytosolic calcium ([Ca(2+)](cyto)) as a key signal for egg activation and a polyspermy block in animal oocytes. Fertilization in flowering plants is more complex, involving interaction of a pollen tube with egg adjoining synergid cells, culminating in release of two sperm cells and their fusion with the egg and central cell, respectively. Here, we report the occurrence and role of [Ca(2+)](cyto) signals during the entire double fertilization process in Arabidopsis. [Ca(2+)](cyto) oscillations are initiated in synergid cells after physical contact with the pollen tube apex. In egg and central cells, a short [Ca(2+)](cyto) transient is associated with pollen tube burst and sperm cell arrival. A second extended [Ca(2+)](cyto) transient solely in the egg cell is correlated with successful fertilization. Thus, each female cell type involved in double fertilization displays a characteristic [Ca(2+)](cyto) signature differing by timing and behaviour from [Ca(2+)](cyto) waves reported in mammals. Nature Pub. Group 2014-08-22 /pmc/articles/PMC4143946/ /pubmed/25145880 http://dx.doi.org/10.1038/ncomms5645 Text en Copyright © 2014, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/
spellingShingle Article
Denninger, Philipp
Bleckmann, Andrea
Lausser, Andreas
Vogler, Frank
Ott, Thomas
Ehrhardt, David W.
Frommer, Wolf B.
Sprunck, Stefanie
Dresselhaus, Thomas
Grossmann, Guido
Male–female communication triggers calcium signatures during fertilization in Arabidopsis
title Male–female communication triggers calcium signatures during fertilization in Arabidopsis
title_full Male–female communication triggers calcium signatures during fertilization in Arabidopsis
title_fullStr Male–female communication triggers calcium signatures during fertilization in Arabidopsis
title_full_unstemmed Male–female communication triggers calcium signatures during fertilization in Arabidopsis
title_short Male–female communication triggers calcium signatures during fertilization in Arabidopsis
title_sort male–female communication triggers calcium signatures during fertilization in arabidopsis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4143946/
https://www.ncbi.nlm.nih.gov/pubmed/25145880
http://dx.doi.org/10.1038/ncomms5645
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