Evidence map›Paper›PMID 41660012›Full record

ArticleFrontiers in cell and developmental biology2025

BMP and NODAL paracrine signalling regulate the totipotent-like cell state in embryonic stem cells.

Sanidhya Jagdish, Loick Joumier, Sabin Dhakal, Gilberto Duran-Bishop, Mohammed Usama, Mohan Malleshaiah

Abstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2025. 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.

Sanidhya Jagdish *Institut de recherches cliniques de Montréal (IRCM), Montreal, QC, Canada.
Loick Joumier *Institut de recherches cliniques de Montréal (IRCM), Montreal, QC, Canada.
Sabin DhakalInstitut de recherches cliniques de Montréal (IRCM), Montreal, QC, Canada.
Gilberto Duran-BishopInstitut de recherches cliniques de Montréal (IRCM), Montreal, QC, Canada.
Mohammed UsamaInstitut de recherches cliniques de Montréal (IRCM), Montreal, QC, Canada.
Mohan MalleshaiahInstitut de recherches cliniques de Montréal (IRCM), Montreal, QC, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cell-cell communication coordinates signalling between cells to guide context-dependent cell fate decisions such as proliferation, differentiation, and lineage specification. Such communication mechanisms are poorly understood in regulating the stem cell states. In this study, we investigate how cell-cell communication regulates cell fate transitions in heterogeneous embryonic stem cell populations, with a particular focus on totipotent-like cells that resemble the two-cell stage embryo. Using single-cell RNA sequencing in combination with computational frameworks, we map ligand-receptor interactions and model downstream regulatory effects across various stem cell states. We functionally validate the predictions by selectively perturbing signalling pathways under specific culture conditions. Our data reveal the key roles of BMP and NODAL (TGF-β) signalling in mediating intercellular communication to shape stem cell identity and heterogeneity. These findings enhance our understanding of the signalling logic that governs early developmental cell fate decisions, providing new insights into stem cell biology with broad implications for regenerative medicine and developmental modelling.

Indexed as

bone morphonegentic protein (BMP) Signallingembryonic stem cellsnodal signallingparacrine signallingtotipotent-like cell state

Identifiers

PMID41660012
PMCPMC12876259

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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.