Evidence map›Paper›PMID 29123210›Full record

ArticleScientific reports2017

Plasticity of the inner cell mass in mouse blastocyst is restricted by the activity of FGF/MAPK pathway.

M Wigger, K Kisielewska, K Filimonow, B Plusa, M Maleszewski, A Suwińska

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

23 citing papers in PubMed, 52 citations in OpenAlex.

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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

6 authors at 3 institutions in 2 countries.

M WiggerDepartment of Embryology, Faculty of Biology, University of Warsaw, Warsaw, Poland.
K KisielewskaDepartment of Embryology, Faculty of Biology, University of Warsaw, Warsaw, Poland.
K FilimonowDepartment of Embryology, Faculty of Biology, University of Warsaw, Warsaw, Poland.
B PlusaFaculty of Life Sciences, University of Manchester, Manchester, UK.
M MaleszewskiDepartment of Embryology, Faculty of Biology, University of Warsaw, Warsaw, Poland.
A SuwińskaDepartment of Embryology, Faculty of Biology, University of Warsaw, Warsaw, Poland. asuwinska@biol.uw.edu.pl.
University of Warsaw · PLUniversity of Manchester · GBPolish Academy of Sciences · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In order to ensure successful development, cells of the early mammalian embryo must differentiate to either trophectoderm (TE) or inner cell mass (ICM), followed by epiblast (EPI) or primitive endoderm (PE) specification within the ICM. Here, we deciphered the mechanism that assures the correct order of these sequential cell fate decisions. We revealed that TE-deprived ICMs derived from 32-cell blastocysts are still able to reconstruct TE during in vitro culture, confirming totipotency of ICM cells at this stage. ICMs isolated from more advanced blastocysts no longer retain totipotency, failing to form TE and generating PE on their surface. We demonstrated that the transition from full potency to lineage priming is prevented by inhibition of the FGF/MAPK signalling pathway. Moreover, we found that after this first restriction step, ICM cells still retain fate flexibility, manifested by ability to convert their fate into an alternative lineage (PE towards EPI and vice versa), until peri-implantation stage.

Indexed as

Cell DifferentiationAnimalsBlastocystFibroblast Growth FactorsMice, Inbred C57BLMitogen-Activated Protein KinasesSignal TransductionTotipotent Stem CellsFibroblast Growth FactorsMitogen-Activated Protein Kinases

Identifiers

PMID29123210
PMCPMC5680175
OpenAlexW2767203015

What Socratic holds

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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 Socratic graph.