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Ca(2+) dynamics in oocytes from naturally-aged mice

The ability of human metaphase-II arrested eggs to activate following fertilisation declines with advancing maternal age. Egg activation is triggered by repetitive increases in intracellular Ca(2+) concentration ([Ca(2+)](i)) in the ooplasm as a result of sperm-egg fusion. We therefore hypothesised...

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Autores principales: Haverfield, Jenna, Nakagawa, Shoma, Love, Daniel, Tsichlaki, Elina, Nomikos, Michail, Lai, F. Anthony, Swann, Karl, FitzHarris, Greg
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4726220/
https://www.ncbi.nlm.nih.gov/pubmed/26785810
http://dx.doi.org/10.1038/srep19357
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author Haverfield, Jenna
Nakagawa, Shoma
Love, Daniel
Tsichlaki, Elina
Nomikos, Michail
Lai, F. Anthony
Swann, Karl
FitzHarris, Greg
author_facet Haverfield, Jenna
Nakagawa, Shoma
Love, Daniel
Tsichlaki, Elina
Nomikos, Michail
Lai, F. Anthony
Swann, Karl
FitzHarris, Greg
author_sort Haverfield, Jenna
collection PubMed
description The ability of human metaphase-II arrested eggs to activate following fertilisation declines with advancing maternal age. Egg activation is triggered by repetitive increases in intracellular Ca(2+) concentration ([Ca(2+)](i)) in the ooplasm as a result of sperm-egg fusion. We therefore hypothesised that eggs from older females feature a reduced ability to mount appropriate Ca(2+) responses at fertilisation. To test this hypothesis we performed the first examination of Ca(2+) dynamics in eggs from young and naturally-aged mice. Strikingly, we find that Ca(2+) stores and resting [Ca(2+)](i) are unchanged with age. Although eggs from aged mice feature a reduced ability to replenish intracellular Ca(2+) stores following depletion, this difference had no effect on the duration, number, or amplitude of Ca(2+) oscillations following intracytoplasmic sperm injection or expression of phospholipase C zeta. In contrast, we describe a substantial reduction in the frequency and duration of oscillations in aged eggs upon parthenogenetic activation with SrCl(2). We conclude that the ability to mount and respond to an appropriate Ca(2+) signal at fertilisation is largely unchanged by advancing maternal age, but subtle changes in Ca(2+) handling occur that may have more substantial impacts upon commonly used means of parthenogenetic activation.
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spelling pubmed-47262202016-01-27 Ca(2+) dynamics in oocytes from naturally-aged mice Haverfield, Jenna Nakagawa, Shoma Love, Daniel Tsichlaki, Elina Nomikos, Michail Lai, F. Anthony Swann, Karl FitzHarris, Greg Sci Rep Article The ability of human metaphase-II arrested eggs to activate following fertilisation declines with advancing maternal age. Egg activation is triggered by repetitive increases in intracellular Ca(2+) concentration ([Ca(2+)](i)) in the ooplasm as a result of sperm-egg fusion. We therefore hypothesised that eggs from older females feature a reduced ability to mount appropriate Ca(2+) responses at fertilisation. To test this hypothesis we performed the first examination of Ca(2+) dynamics in eggs from young and naturally-aged mice. Strikingly, we find that Ca(2+) stores and resting [Ca(2+)](i) are unchanged with age. Although eggs from aged mice feature a reduced ability to replenish intracellular Ca(2+) stores following depletion, this difference had no effect on the duration, number, or amplitude of Ca(2+) oscillations following intracytoplasmic sperm injection or expression of phospholipase C zeta. In contrast, we describe a substantial reduction in the frequency and duration of oscillations in aged eggs upon parthenogenetic activation with SrCl(2). We conclude that the ability to mount and respond to an appropriate Ca(2+) signal at fertilisation is largely unchanged by advancing maternal age, but subtle changes in Ca(2+) handling occur that may have more substantial impacts upon commonly used means of parthenogenetic activation. Nature Publishing Group 2016-01-20 /pmc/articles/PMC4726220/ /pubmed/26785810 http://dx.doi.org/10.1038/srep19357 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
Haverfield, Jenna
Nakagawa, Shoma
Love, Daniel
Tsichlaki, Elina
Nomikos, Michail
Lai, F. Anthony
Swann, Karl
FitzHarris, Greg
Ca(2+) dynamics in oocytes from naturally-aged mice
title Ca(2+) dynamics in oocytes from naturally-aged mice
title_full Ca(2+) dynamics in oocytes from naturally-aged mice
title_fullStr Ca(2+) dynamics in oocytes from naturally-aged mice
title_full_unstemmed Ca(2+) dynamics in oocytes from naturally-aged mice
title_short Ca(2+) dynamics in oocytes from naturally-aged mice
title_sort ca(2+) dynamics in oocytes from naturally-aged mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4726220/
https://www.ncbi.nlm.nih.gov/pubmed/26785810
http://dx.doi.org/10.1038/srep19357
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