Evidence map›Paper›PMID 41687620›Full record

ArticleStem cell reports2026

Exit from naive pluripotency proceeds with variable latency but without asymmetric division to generate population heterogeneity.

Stanley E Strawbridge, Clelia Corridori, Guy B Blanchard, Austin Smith, Hillel Kugler, Graziano Martello

Abstract read
In one paragraph

Article in Stem cell reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Stanley E StrawbridgeWellcome-MRC Cambridge Stem Cell Institute, Jeffrey Cheah Biomedical Centre, University of Cambridge, Cambridge CB2 0AW, UK; Department of Biochemistry, University of Cambridge, Cambridge CB2 1QR, UK.
Clelia CorridoriDepartment of Biology, University of Padua, Padua, Italy.
Guy B BlanchardDepartment of Physiology, Development and Neuroscience, University of Cambridge, Cambridge CB2 3DY, UK.
Austin SmithLiving Systems Institute and Department of Biosciences, University of Exeter, Exeter EX4 4QD, UK. Electronic address: austin.smith@exeter.ac.uk.
Hillel KuglerFaculty of Engineering, Bar-Ilan University, Ramat Gan 5290002, Israel. Electronic address: hillelk@biu.ac.il.
Graziano MartelloDepartment of Biology, University of Padua, Padua, Italy. Electronic address: graziano.martello@unipd.it.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mouse embryonic stem (ES) cells are pluripotent cell lines established from the preimplantation epiblast. ES cells undergo transition from naive to formative pluripotency in defined conditions. Here, we used the Rex1-GFPd2 (RGd2) fluorescent reporter to track ES cells traversing the cell state boundary by long-term single-cell imaging (LTSCI). We saw no reporter re-expression, indicating irreversible differentiation. We observed only symmetric divisions, consistent with a simple population dynamics model. Genealogical analysis showed that transitions were highly correlated between sister cells. The collapse of naive identity was invariably abrupt but was preceded by a variable lag period. Across the population, however, exit times varied by more than 15 h. The delay in entering transition extended up to three generations. Thus, ES cell differentiation timing is not directly determined by cell cycle. We speculate that asynchronous departure from the naive state may safeguard pluripotency progression in the embryo founder population.

Indexed as

Asymmetric Cell DivisionMouse Embryonic Stem CellsPluripotent Stem CellsAnimalsCell DifferentiationCell DivisionMicecell trackingcommitmentdifferentiationembryonic stem cellsformative pluripotencymathematical modelingmathematical modellingstem cellssymmetric division

Identifiers

PMID41687620
PMCPMC12985371

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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.