Evidence map›Paper›PMID 29748644›Full record

ArticleScientific reports2018

Live-cell imaging of nuclear-chromosomal dynamics in bovine in vitro fertilised embryos.

Tatsuma Yao, Rie Suzuki, Natsuki Furuta, Yuka Suzuki, Kyoko Kabe, Mikiko Tokoro, Atsushi Sugawara, Akira Yajima, Tomohiro Nagasawa, Satoko Matoba and 2 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

20 citing papers in PubMed, 35 citations in OpenAlex.

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  13. Pre-Implantation Bovine Embryo Evaluation-From Optics to Omics and Beyond.Animals : an open access journal from MDPI · 2023
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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

12 authors at 5 institutions in 2 countries.

Tatsuma YaoFaculty of Biology-Oriented Science and Technology (BOST), Kindai University, Wakayama, Japan.
Rie SuzukiFaculty of Biology-Oriented Science and Technology (BOST), Kindai University, Wakayama, Japan.
Natsuki FurutaFaculty of Biology-Oriented Science and Technology (BOST), Kindai University, Wakayama, Japan.
Yuka SuzukiFaculty of Biology-Oriented Science and Technology (BOST), Kindai University, Wakayama, Japan.
Kyoko KabeFaculty of Biology-Oriented Science and Technology (BOST), Kindai University, Wakayama, Japan.
Mikiko TokoroFaculty of Biology-Oriented Science and Technology (BOST), Kindai University, Wakayama, Japan.
Atsushi SugawaraDepartment of Biological Production, Tokyo University of Agriculture and Technology, Tokyo, Japan.
Akira YajimaDepartment of Biological Production, Tokyo University of Agriculture and Technology, Tokyo, Japan.
Tomohiro NagasawaDepartment of Biological Production, Tokyo University of Agriculture and Technology, Tokyo, Japan.
Satoko MatobaDivision of Animal Breeding and Reproduction Research, Institute of Livestock and Grassland Science, NARO (NILGS), Ibaraki, Japan.
Kazuo YamagataFaculty of Biology-Oriented Science and Technology (BOST), Kindai University, Wakayama, Japan. yamagata@waka.kindai.ac.jp.
Satoshi SugimuraDepartment of Biological Production, Tokyo University of Agriculture and Technology, Tokyo, Japan. satoshis@cc.tuat.ac.jp.ORCID 0000-0002-6473-5941
Kindai University · JPTokyo University of Agriculture and Technology · JPFuso Pharmaceutical Industries (Japan) · JPInstitute of Livestock and Grassland Science · JPUniversity of Hawaii System · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nuclear/chromosomal integrity is an important prerequisite for the assessment of embryo quality in artificial reproductive technology. However, lipid-rich dark cytoplasm in bovine embryos prevents its observation by visible light microscopy. We performed live-cell imaging using confocal laser microscopy that allowed long-term imaging of nuclear/chromosomal dynamics in bovine in vitro fertilised (IVF) embryos. We analysed the relationship between nuclear/chromosomal aberrations and in vitro embryonic development and morphological blastocyst quality. Three-dimensional live-cell imaging of 369 embryos injected with mRNA encoding histone H2B-mCherry and enhanced green fluorescent protein (EGFP)-α-tubulin was performed from single-cell to blastocyst stage for eight days; 17.9% reached the blastocyst stage. Abnormalities in the number of pronuclei (PN), chromosomal segregation, cytokinesis, and blastomere number at first cleavage were observed at frequencies of 48.0%, 30.6%, 8.1%, and 22.2%, respectively, and 13.0%, 6.2%, 3.3%, and 13.4%, respectively, for abnormal embryos developed into blastocysts. A multivariate analysis showed that abnormal chromosome segregation (ACS) and multiple PN correlated with delayed timing and abnormal blastomere number at first cleavage, respectively. In morphologically transferrable blastocysts, 30-40% of embryos underwent ACS and had abnormal PN. Live-cell imaging may be useful for analysing the association between nuclear/chromosomal dynamics and embryonic development in bovine embryos.

Indexed as

Chromosome SegregationFertilization in VitroAnimalsCattleCell SurvivalChromosome AberrationsEmbryo, MammalianFemaleGreen Fluorescent ProteinsLuminescent ProteinsMicroscopy, ConfocalOptical ImagingPregnancyRed Fluorescent Proteinenhanced green fluorescent proteinGreen Fluorescent ProteinsLuminescent ProteinsRed Fluorescent Protein

Identifiers

PMID29748644
PMCPMC5945782
OpenAlexW2806991087

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.