Evidence map›Paper›PMID 27151947›Full record

ArticleDevelopment (Cambridge, England)2016

Quantitative imaging of lipids in live mouse oocytes and early embryos using CARS microscopy.

Josephine Bradley, Iestyn Pope, Francesco Masia, Randa Sanusi, Wolfgang Langbein, Karl Swann, Paola Borri

Open access · hybridAbstract read
In one paragraph

Article in Development (Cambridge, England), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
13.6field-weighted citation impact, top 1% of its field
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

41 citing papers in PubMed, 79 citations in OpenAlex.

  1. Review
  2. Review
  3. Micro magnetic resonance spectroscopy for noninvasive metabolic screening of mammalian embryos and oocytes.Proceedings of the National Academy of Sciences of the United States of America · 2025
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  16. Nile Red and BODIPY Staining of Lipid Droplets in Mouse Oocytes and Embryos.Methods in molecular biology (Clifton, N.J.) · 2023
    Article
  17. Article
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  20. Review
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

7 authors at 1 institution in 1 country.

Josephine BradleyCardiff School of Biosciences, The Sir Martin Evans Building, Museum Avenue, Cardiff CF10 3AX, UK.
Iestyn PopeCardiff School of Biosciences, The Sir Martin Evans Building, Museum Avenue, Cardiff CF10 3AX, UK.
Francesco MasiaCardiff School of Physics and Astronomy, The Parade, Cardiff CF24 3AA, UK.
Randa SanusiCardiff University School of Medicine, Sir Geraint Evans Building, Heath Park, Cardiff CF14 4XN, UK.
Wolfgang LangbeinCardiff School of Physics and Astronomy, The Parade, Cardiff CF24 3AA, UK.
Karl SwannCardiff University School of Medicine, Sir Geraint Evans Building, Heath Park, Cardiff CF14 4XN, UK SwannK1@cardiff.ac.uk BorriP@cardiff.ac.uk.ORCID 0000-0002-4355-1449
Paola BorriCardiff School of Biosciences, The Sir Martin Evans Building, Museum Avenue, Cardiff CF10 3AX, UK SwannK1@cardiff.ac.uk BorriP@cardiff.ac.uk.
Cardiff University · GB

Funding

Biotechnology and Biological Sciences Research Council BB/H006575/1
6 · The paper itself

Abstract

Mammalian oocytes contain lipid droplets that are a store of fatty acids, whose metabolism plays a substantial role in pre-implantation development. Fluorescent staining has previously been used to image lipid droplets in mammalian oocytes and embryos, but this method is not quantitative and often incompatible with live cell imaging and subsequent development. Here we have applied chemically specific, label-free coherent anti-Stokes Raman scattering (CARS) microscopy to mouse oocytes and pre-implantation embryos. We show that CARS imaging can quantify the size, number and spatial distribution of lipid droplets in living mouse oocytes and embryos up to the blastocyst stage. Notably, it can be used in a way that does not compromise oocyte maturation or embryo development. We have also correlated CARS with two-photon fluorescence microscopy simultaneously acquired using fluorescent lipid probes on fixed samples, and found only a partial degree of correlation, depending on the lipid probe, clearly exemplifying the limitation of lipid labelling. In addition, we show that differences in the chemical composition of lipid droplets in living oocytes matured in media supplemented with different saturated and unsaturated fatty acids can be detected using CARS hyperspectral imaging. These results demonstrate that CARS microscopy provides a novel non-invasive method of quantifying lipid content, type and spatial distribution with sub-micron resolution in living mammalian oocytes and embryos.

Indexed as

Imaging, Three-DimensionalSpectrum Analysis, RamanAnimalsCell SurvivalCluster AnalysisEmbryo, MammalianEmbryonic DevelopmentFemaleLipid DropletsLipidsMiceMicroscopyMicroscopy, FluorescenceOocytesLipidsEggEmbryoLipidMicroscopyOocyte

Identifiers

PMID27151947
PMCPMC4920167
OpenAlexW2346679282

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.