Evidence map›Paper›PMID 26785810›Full record

ArticleScientific reports2016

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

Jenna Haverfield, Shoma Nakagawa, Daniel Love, Elina Tsichlaki, Michail Nomikos, F Anthony Lai, Karl Swann, Greg FitzHarris

Abstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Superovulation Does Not Alter Calcium Oscillations Following Fertilization.Frontiers in cell and developmental biology · 2021
    Article
  5. Article
  6. Article
  7. Review
  8. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Jenna HaverfieldCentre Recherche Centre Hospitalier Université de Montréal, Montreal, Québec, Canada, H2X 0A9.
Shoma NakagawaCentre Recherche Centre Hospitalier Université de Montréal, Montreal, Québec, Canada, H2X 0A9.
Daniel LoveInstitute of Molecular and Experimental Medicine, Cardiff University School of Medicine, Heath Park, UK, CF14 4XN.
Elina TsichlakiDepartment of Cell and Developmental Biology, University College London, London, UK, WC1E 6BT.
Michail NomikosInstitute of Molecular and Experimental Medicine, Cardiff University School of Medicine, Heath Park, UK, CF14 4XN.
F Anthony LaiInstitute of Molecular and Experimental Medicine, Cardiff University School of Medicine, Heath Park, UK, CF14 4XN.
Karl SwannInstitute of Molecular and Experimental Medicine, Cardiff University School of Medicine, Heath Park, UK, CF14 4XN.
Greg FitzHarrisCentre Recherche Centre Hospitalier Université de Montréal, Montreal, Québec, Canada, H2X 0A9.

Funding

Canadian Institutes of Health ResearchMedical Research Council
6 · The paper itself

Abstract

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 SrCl2. 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.

Indexed as

Calcium SignalingAge FactorsAnimalsCalciumFemaleIntracellular SpaceMaleMiceOocytesOvumSperm Injections, IntracytoplasmicCalcium

Identifiers

PMID26785810
PMCPMC4726220

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.