Evidence map›Paper›PMID 38368368›Full record

ArticleNature communications2024

Time-integrated BMP signaling determines fate in a stem cell model for early human development.

Seth Teague, Gillian Primavera, Bohan Chen, Zong-Yuan Liu, LiAng Yao, Emily Freeburne, Hina Khan, Kyoung Jo, Craig Johnson, Idse Heemskerk

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
10.8field-weighted citation impact, top 1% 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

35 citing papers in PubMed, 47 citations in OpenAlex.

  1. Review
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  12. Thermogenesis is limited by cellular competence.Frontiers in cell and developmental biology · 2026
    Article
  13. Optogenetic Rescue Reveals Spatiotemporal Rules of Germ-Layer Patterning.bioRxiv : the preprint server for biology · 2025
    Article
  14. Review
  15. Article
  16. Dynamical systems of fate and form in development.Seminars in cell & developmental biology · 2025
    Review
  17. Article
  18. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 1 institution in 1 country.

Seth TeagueDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, MI, USA.ORCID 0000-0002-0973-1251
Gillian PrimaveraDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, MI, USA.
Bohan ChenDepartment of Computational Medicine and Bioinformatics, University of Michigan Medical School, Ann Arbor, MI, USA.ORCID 0000-0002-9781-2982
Zong-Yuan LiuDepartment of Cell and Developmental Biology, University of Michigan Medical School, Ann Arbor, MI, USA.
LiAng YaoDepartment of Cell and Developmental Biology, University of Michigan Medical School, Ann Arbor, MI, USA.
Emily FreeburneDepartment of Cell and Developmental Biology, University of Michigan Medical School, Ann Arbor, MI, USA.
Hina KhanDepartment of Cell and Developmental Biology, University of Michigan Medical School, Ann Arbor, MI, USA.
Kyoung JoDepartment of Cell and Developmental Biology, University of Michigan Medical School, Ann Arbor, MI, USA.
Craig JohnsonDepartment of Cell and Developmental Biology, University of Michigan Medical School, Ann Arbor, MI, USA.
Idse HeemskerkDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, MI, USA. iheemske@umich.edu.ORCID 0000-0002-8861-7712
University of Michigan · US

Funding

Multifunctional morphogens: patterning precision and mesoderm migrationR35GM138346 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI HEEMSKERK, IDSE JOANNES · 2020 to 2025
$4.3M
Cellular Biotechnology Training Program (CBTP) - Years 31-35T32GM145304 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Guizhi Zhu · 2022 to 2026
$2.6M
Dynamics of FGF and its integration with other pathways during human germ layer differentiationF32HD108980 · NICHD · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI JO, KYOUNG HA · 2022 to 2023
$159k
NICHD NIH HHS F32 HD108980NIGMS NIH HHS R35 GM138346NIGMS NIH HHS T32 GM145304
6 · The paper itself

Abstract

How paracrine signals are interpreted to yield multiple cell fate decisions in a dynamic context during human development in vivo and in vitro remains poorly understood. Here we report an automated tracking method to follow signaling histories linked to cell fate in large numbers of human pluripotent stem cells (hPSCs). Using an unbiased statistical approach, we discover that measured BMP signaling history correlates strongly with fate in individual cells. We find that BMP response in hPSCs varies more strongly in the duration of signaling than the level. However, both the level and duration of signaling activity control cell fate choices only by changing the time integral. Therefore, signaling duration and level are interchangeable in this context. In a stem cell model for patterning of the human embryo, we show that signaling histories predict the fate pattern and that the integral model correctly predicts changes in cell fate domains when signaling is perturbed. Our data suggest that mechanistically, BMP signaling is integrated by SOX2.

Indexed as

Pluripotent Stem CellsCell DifferentiationHumansSignal Transduction

Identifiers

PMID38368368
PMCPMC10874454
OpenAlexW4391899537

What Socratic 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 Socratic graph.