Cargando…

The zinc spark is an inorganic signature of human egg activation

Egg activation refers to events required for transition of a gamete into an embryo, including establishment of the polyspermy block, completion of meiosis, entry into mitosis, selective recruitment and degradation of maternal mRNA, and pronuclear development. Here we show that zinc fluxes accompany...

Descripción completa

Detalles Bibliográficos
Autores principales: Duncan, Francesca E., Que, Emily L., Zhang, Nan, Feinberg, Eve C., O’Halloran, Thomas V., Woodruff, Teresa K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4845039/
https://www.ncbi.nlm.nih.gov/pubmed/27113677
http://dx.doi.org/10.1038/srep24737
_version_ 1782428867137372160
author Duncan, Francesca E.
Que, Emily L.
Zhang, Nan
Feinberg, Eve C.
O’Halloran, Thomas V.
Woodruff, Teresa K.
author_facet Duncan, Francesca E.
Que, Emily L.
Zhang, Nan
Feinberg, Eve C.
O’Halloran, Thomas V.
Woodruff, Teresa K.
author_sort Duncan, Francesca E.
collection PubMed
description Egg activation refers to events required for transition of a gamete into an embryo, including establishment of the polyspermy block, completion of meiosis, entry into mitosis, selective recruitment and degradation of maternal mRNA, and pronuclear development. Here we show that zinc fluxes accompany human egg activation. We monitored calcium and zinc dynamics in individual human eggs using selective fluorophores following activation with calcium-ionomycin, ionomycin, or hPLCζ cRNA microinjection. These egg activation methods, as expected, induced rises in intracellular calcium levels and also triggered the coordinated release of zinc into the extracellular space in a prominent “zinc spark.” The ability of the gamete to mount a zinc spark response was meiotic-stage dependent. Moreover, chelation of intracellular zinc alone was sufficient to induce cell cycle resumption and transition of a meiotic cell into a mitotic one. Together, these results demonstrate critical functions for zinc dynamics and establish the zinc spark as an extracellular marker of early human development.
format Online
Article
Text
id pubmed-4845039
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-48450392016-04-29 The zinc spark is an inorganic signature of human egg activation Duncan, Francesca E. Que, Emily L. Zhang, Nan Feinberg, Eve C. O’Halloran, Thomas V. Woodruff, Teresa K. Sci Rep Article Egg activation refers to events required for transition of a gamete into an embryo, including establishment of the polyspermy block, completion of meiosis, entry into mitosis, selective recruitment and degradation of maternal mRNA, and pronuclear development. Here we show that zinc fluxes accompany human egg activation. We monitored calcium and zinc dynamics in individual human eggs using selective fluorophores following activation with calcium-ionomycin, ionomycin, or hPLCζ cRNA microinjection. These egg activation methods, as expected, induced rises in intracellular calcium levels and also triggered the coordinated release of zinc into the extracellular space in a prominent “zinc spark.” The ability of the gamete to mount a zinc spark response was meiotic-stage dependent. Moreover, chelation of intracellular zinc alone was sufficient to induce cell cycle resumption and transition of a meiotic cell into a mitotic one. Together, these results demonstrate critical functions for zinc dynamics and establish the zinc spark as an extracellular marker of early human development. Nature Publishing Group 2016-04-26 /pmc/articles/PMC4845039/ /pubmed/27113677 http://dx.doi.org/10.1038/srep24737 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 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/4.0/
spellingShingle Article
Duncan, Francesca E.
Que, Emily L.
Zhang, Nan
Feinberg, Eve C.
O’Halloran, Thomas V.
Woodruff, Teresa K.
The zinc spark is an inorganic signature of human egg activation
title The zinc spark is an inorganic signature of human egg activation
title_full The zinc spark is an inorganic signature of human egg activation
title_fullStr The zinc spark is an inorganic signature of human egg activation
title_full_unstemmed The zinc spark is an inorganic signature of human egg activation
title_short The zinc spark is an inorganic signature of human egg activation
title_sort zinc spark is an inorganic signature of human egg activation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4845039/
https://www.ncbi.nlm.nih.gov/pubmed/27113677
http://dx.doi.org/10.1038/srep24737
work_keys_str_mv AT duncanfrancescae thezincsparkisaninorganicsignatureofhumaneggactivation
AT queemilyl thezincsparkisaninorganicsignatureofhumaneggactivation
AT zhangnan thezincsparkisaninorganicsignatureofhumaneggactivation
AT feinbergevec thezincsparkisaninorganicsignatureofhumaneggactivation
AT ohalloranthomasv thezincsparkisaninorganicsignatureofhumaneggactivation
AT woodruffteresak thezincsparkisaninorganicsignatureofhumaneggactivation
AT duncanfrancescae zincsparkisaninorganicsignatureofhumaneggactivation
AT queemilyl zincsparkisaninorganicsignatureofhumaneggactivation
AT zhangnan zincsparkisaninorganicsignatureofhumaneggactivation
AT feinbergevec zincsparkisaninorganicsignatureofhumaneggactivation
AT ohalloranthomasv zincsparkisaninorganicsignatureofhumaneggactivation
AT woodruffteresak zincsparkisaninorganicsignatureofhumaneggactivation