Evidence map›Paper›PMID 41493481›Full record

ReviewCellular and molecular life sciences : CMLS2026

Exiting the ground state: the broad spectrum of cell fates accessible from naïve human pluripotent stem cells.

Kyoung-Mi Park, Richard Yin, Thorold W Theunissen

Abstract readReview
In one paragraph

Review in Cellular and molecular life sciences : CMLS, 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

3 authors.

Kyoung-Mi ParkDepartment of Developmental Biology and Center of Regenerative Medicine, Washington University School of Medicine, St. Louis, MO, 63110, USA.
Richard YinDepartment of Developmental Biology and Center of Regenerative Medicine, Washington University School of Medicine, St. Louis, MO, 63110, USA.
Thorold W TheunissenDepartment of Developmental Biology and Center of Regenerative Medicine, Washington University School of Medicine, St. Louis, MO, 63110, USA. t.theunissen@wustl.edu.ORCID http://orcid.org/0000-0001-6943-7858

Funding

Resolving epigenetic instability during pluripotent state transitions: a roadmap for exploiting the biomedical potential of dynamic human stem cell statesR35GM153439 · NIGMS · WASHINGTON UNIVERSITY · PI Thorold Theunissen · 2024 to 2026
$1.3M
Modeling Human Trophoblast Differentiation and Function Using Pluripotent Stem CellsR01HD119277 · NICHD · WASHINGTON UNIVERSITY · PI Sabine M Dietmann, Kristen L Kroll · 2025 to 2026
$1.3M
Mechanisms of X chromosome inactivation during human trophoblast differentiation in vitroR21HD112754 · NICHD · WASHINGTON UNIVERSITY · PI THEUNISSEN, THOROLD · 2023 to 2023
$428k
Edward Mallinckrodt, Jr. Foundation Mallinckrodt Scholar AwardEunice Kennedy Shriver National Institute of Child Health and Human Development R01HD119277-01National Institute of Child Health and Human Development 1R21HD112754-01NICHD NIH HHS R01 HD119277NICHD NIH HHS R21 HD112754NIGMS NIH HHS R35 GM153439NIGMS NIH HHS R35GM153439-01
6 · The paper itself

Abstract

Naïve human pluripotent stem cells (hPSCs) represent an in vitro analog of the pre-implantation epiblast - the founder tissue of the embryo proper. A widely held assumption, based on prior studies in the mouse system, was that naïve hPSCs are restricted in their differentiation potential toward more mature stages of epiblast development, as a prelude to gastrulation. However, over the past 5 years, a growing body of literature has demonstrated that naïve hPSCs have an expanded lineage potential toward a broad range of embryonic and extraembryonic fates and can even be used as a starting point for generating 8-cell-like cells. The most emphatic demonstration of the broad lineage potential of naïve hPSCs is their remarkable capacity to self-organize into blastocyst-like structures ("blastoids") that model all three lineages of the pre-implantation embryo and can be cultured to post-implantation stages. Here, we discuss the broad spectrum of cell fates accessible from naïve hPSCs and the signaling pathways that guide the exit from the ground state of human pluripotency.

Indexed as

Cell DifferentiationCell LineagePluripotent Stem CellsAnimalsHumans8-cell-like cellsAmnionBlastoidsCapacitationEpiblastExtraembryonic mesodermhPGCLCsHypoblastNaïve pluripotencyPluripotent stem cellsTrophectodermTrophoblast

Identifiers

PMID41493481
PMCPMC12775239

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Registered trials

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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.