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

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

PMC · DOI: 10.3389/fcell.2025.1720355 · Frontiers in Cell and Developmental Biology · 2026-01-23

## TL;DR

This study shows how BMP and NODAL signals help embryonic stem cells maintain a totipotent-like state, resembling early embryos.

## Contribution

The study identifies BMP and NODAL signaling as key regulators of intercellular communication in stem cell heterogeneity and identity.

## Key findings

- BMP and NODAL signaling mediate intercellular communication in stem cell populations.
- These signals regulate the totipotent-like cell state resembling two-cell stage embryos.
- Perturbing these pathways alters stem cell identity and heterogeneity.

## 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.

## Linked entities

- **Proteins:** dpp (decapentaplegic), NODAL (nodal growth differentiation factor), TGFB1 (transforming growth factor beta 1)

## Full-text entities

- **Genes:** TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040] {aka CAEND1, CED, DPD1, IBDIMDE, LAP, TGF-beta1}, BMP1 (bone morphogenetic protein 1) [NCBI Gene 649] {aka OI13, PCOLC, PCP, TLD}, NODAL (nodal growth differentiation factor) [NCBI Gene 4838] {aka HTX5}

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12876259/full.md

## References

66 references — full list in the complete paper: https://tomesphere.com/paper/PMC12876259/full.md

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Source: https://tomesphere.com/paper/PMC12876259