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Quantitative mapping of zinc fluxes in the mammalian egg reveals the origin of fertilization-induced zinc sparks

Fertilization of a mammalian egg induces a series of ‘zinc sparks’ that are necessary for inducing the egg-to-embryo transition. Despite the importance of these zinc efflux events little is known about their origin. To understand the molecular mechanism of the zinc spark we combined four physical ap...

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Autores principales: Que, Emily L., Bleher, Reiner, Duncan, Francesca E., Kong, Betty Y., Gleber, Sophie C., Vogt, Stefan, Chen, Si, Garwin, Seth A., Bayer, Amanda R., Dravid, Vinayak, Woodruff, Teresa K., O’Halloran, Thomas V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4315321/
https://www.ncbi.nlm.nih.gov/pubmed/25615666
http://dx.doi.org/10.1038/nchem.2133
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author Que, Emily L.
Bleher, Reiner
Duncan, Francesca E.
Kong, Betty Y.
Gleber, Sophie C.
Vogt, Stefan
Chen, Si
Garwin, Seth A.
Bayer, Amanda R.
Dravid, Vinayak
Woodruff, Teresa K.
O’Halloran, Thomas V.
author_facet Que, Emily L.
Bleher, Reiner
Duncan, Francesca E.
Kong, Betty Y.
Gleber, Sophie C.
Vogt, Stefan
Chen, Si
Garwin, Seth A.
Bayer, Amanda R.
Dravid, Vinayak
Woodruff, Teresa K.
O’Halloran, Thomas V.
author_sort Que, Emily L.
collection PubMed
description Fertilization of a mammalian egg induces a series of ‘zinc sparks’ that are necessary for inducing the egg-to-embryo transition. Despite the importance of these zinc efflux events little is known about their origin. To understand the molecular mechanism of the zinc spark we combined four physical approaches to resolve zinc distributions in single cells: a chemical probe for dynamic live-cell fluorescence imaging and a combination of scanning transmission electron microscopy with energy dispersive spectroscopy, X-ray fluorescence microscopy, and 3D elemental tomography for high resolution elemental mapping. We show that the zinc spark arises from a system of thousands of zinc-loaded vesicles, each of which contains, on average, 10(6) zinc atoms. These vesicles undergo dynamic movement during oocyte maturation and exocytosis at the time of fertilization. The discovery of these vesicles and the demonstration that zinc sparks originate from them provides a quantitative framework for understanding how zinc fluxes regulate cellular processes.
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spelling pubmed-43153212015-08-01 Quantitative mapping of zinc fluxes in the mammalian egg reveals the origin of fertilization-induced zinc sparks Que, Emily L. Bleher, Reiner Duncan, Francesca E. Kong, Betty Y. Gleber, Sophie C. Vogt, Stefan Chen, Si Garwin, Seth A. Bayer, Amanda R. Dravid, Vinayak Woodruff, Teresa K. O’Halloran, Thomas V. Nat Chem Article Fertilization of a mammalian egg induces a series of ‘zinc sparks’ that are necessary for inducing the egg-to-embryo transition. Despite the importance of these zinc efflux events little is known about their origin. To understand the molecular mechanism of the zinc spark we combined four physical approaches to resolve zinc distributions in single cells: a chemical probe for dynamic live-cell fluorescence imaging and a combination of scanning transmission electron microscopy with energy dispersive spectroscopy, X-ray fluorescence microscopy, and 3D elemental tomography for high resolution elemental mapping. We show that the zinc spark arises from a system of thousands of zinc-loaded vesicles, each of which contains, on average, 10(6) zinc atoms. These vesicles undergo dynamic movement during oocyte maturation and exocytosis at the time of fertilization. The discovery of these vesicles and the demonstration that zinc sparks originate from them provides a quantitative framework for understanding how zinc fluxes regulate cellular processes. 2014-12-15 2015-02 /pmc/articles/PMC4315321/ /pubmed/25615666 http://dx.doi.org/10.1038/nchem.2133 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Que, Emily L.
Bleher, Reiner
Duncan, Francesca E.
Kong, Betty Y.
Gleber, Sophie C.
Vogt, Stefan
Chen, Si
Garwin, Seth A.
Bayer, Amanda R.
Dravid, Vinayak
Woodruff, Teresa K.
O’Halloran, Thomas V.
Quantitative mapping of zinc fluxes in the mammalian egg reveals the origin of fertilization-induced zinc sparks
title Quantitative mapping of zinc fluxes in the mammalian egg reveals the origin of fertilization-induced zinc sparks
title_full Quantitative mapping of zinc fluxes in the mammalian egg reveals the origin of fertilization-induced zinc sparks
title_fullStr Quantitative mapping of zinc fluxes in the mammalian egg reveals the origin of fertilization-induced zinc sparks
title_full_unstemmed Quantitative mapping of zinc fluxes in the mammalian egg reveals the origin of fertilization-induced zinc sparks
title_short Quantitative mapping of zinc fluxes in the mammalian egg reveals the origin of fertilization-induced zinc sparks
title_sort quantitative mapping of zinc fluxes in the mammalian egg reveals the origin of fertilization-induced zinc sparks
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4315321/
https://www.ncbi.nlm.nih.gov/pubmed/25615666
http://dx.doi.org/10.1038/nchem.2133
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