Evidence map›Paper›PMID 30958114›Full record

ArticleOpen biology2019

Embryonic stem cells become mechanoresponsive upon exit from ground state of pluripotency.

C M Verstreken, C Labouesse, C C Agley, K J Chalut

Open access · goldAbstract read
In one paragraph

Article in Open biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.5field-weighted citation impact, top 21% 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

11 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Article
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  5. Review
  6. Epithelial dynamics during early mouse development.Current opinion in genetics & development · 2022
    Review
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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

4 authors at 1 institution in 1 country.

C M Verstreken1 Cavendish Laboratory, Department of Physics, University of Cambridge, Cambridge CB3 0HE, UK.
C Labouesse2 Wellcome Trust/Medical Research Council Stem Cell Institute , University of Cambridge , Cambridge CB2 1QR , UK.
C C Agley2 Wellcome Trust/Medical Research Council Stem Cell Institute , University of Cambridge , Cambridge CB2 1QR , UK.
K J Chalut1 Cavendish Laboratory, Department of Physics, University of Cambridge, Cambridge CB3 0HE, UK.
Wellcome/MRC Cambridge Stem Cell Institute · GB

Funding

Medical Research Council MC_PC_12009Medical Research Council MR/M011089/1Wellcome Trust
6 · The paper itself

Abstract

Stem cell fate decisions are driven by a broad array of signals, both chemical and mechanical. Although much progress has been made in our understanding of the impact of chemical signals on cell fate choice, much less is known about the role and influence of mechanical signalling, particularly in embryonic stem (ES) cells. Many studies use substrates with different stiffness to study mechanical signalling, but changing substrate stiffness can induce secondary effects which are difficult to disentangle from the direct effects of forces/mechanical signals. To probe the direct impact of mechanical stress on cells, we developed an adaptable cell substrate stretcher to exert specific, reproducible forces on cells. Using this device to test the response of ES cells to tensile strain, we found that cells experienced a transient influx of calcium followed by an upregulation of the so-called immediate and early genes. On longer time scales, however, ES cells in ground state conditions were largely insensitive to mechanical stress. Nonetheless, as ES cells exited the ground state, their susceptibility to mechanical signals increased, resulting in broad transcriptional changes. Our findings suggest that exit from ground state of pluripotency is unaffected by mechanical signals, but that these signals could become important during the next stage of lineage specification. A better understanding of this process could improve our understanding of cell fate choice in early development and improve protocols for differentiation guided by mechanical cues.

Indexed as

AnimalsCalciumCell Culture TechniquesCell DifferentiationCells, CulturedMechanical PhenomenaMiceMice, 129 StrainMicroscopy, FluorescenceMouse Embryonic Stem CellsSignal TransductionTime-Lapse ImagingTranscriptional ActivationUp-RegulationCalciumimmediate early genesmechanical signallingmechanosensingpluripotencystem cells

Identifiers

PMID30958114
PMCPMC6367133
OpenAlexW2909341781

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.