Evidence map›Paper›PMID 41022819›Full record

ArticleNature communications2025

Contractile fibroblasts form a transient niche for the branching mammary epithelium.

Jakub Sumbal, Robin P Journot, Kriti Attri, Veronika Danek, Candice Merle, Marisa M Faraldo, Zuzana Sumbalova Koledova, Silvia Fre

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Review
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

8 authors.

Jakub SumbalInstitut Curie, Laboratory of Genetics and Developmental Biology, INSERM U934, CNRS UMR3215, PSL University, Sorbonne University, Paris, France.ORCID http://orcid.org/0000-0003-3700-4518
Robin P JournotInstitut Curie, Laboratory of Genetics and Developmental Biology, INSERM U934, CNRS UMR3215, PSL University, Sorbonne University, Paris, France.ORCID http://orcid.org/0000-0002-1967-2400
Kriti AttriInstitute of Molecular Genetics of the Czech Academy of Sciences, Laboratory of Tissue Morphogenesis and Cancer, Prague, Czech Republic.ORCID http://orcid.org/0009-0005-7289-1679
Veronika DanekInstitute of Molecular Genetics of the Czech Academy of Sciences, Laboratory of Tissue Morphogenesis and Cancer, Prague, Czech Republic.ORCID http://orcid.org/0009-0000-7759-5696
Candice MerleInstitut Curie, Laboratory of Genetics and Developmental Biology, INSERM U934, CNRS UMR3215, PSL University, Sorbonne University, Paris, France.ORCID http://orcid.org/0000-0001-9103-6671
Marisa M FaraldoInstitut Curie, Laboratory of Genetics and Developmental Biology, INSERM U934, CNRS UMR3215, PSL University, Sorbonne University, Paris, France.ORCID http://orcid.org/0000-0001-9497-1171
Zuzana Sumbalova Koledova *Institute of Molecular Genetics of the Czech Academy of Sciences, Laboratory of Tissue Morphogenesis and Cancer, Prague, Czech Republic. zuzana.sumbalova-koledova@img.cas.cz.ORCID http://orcid.org/0000-0002-9333-1399
Silvia Fre *Institut Curie, Laboratory of Genetics and Developmental Biology, INSERM U934, CNRS UMR3215, PSL University, Sorbonne University, Paris, France. silvia.fre@curie.fr.ORCID http://orcid.org/0000-0002-7209-7636

Funding

Agence Nationale de la Recherche (French National Research Agency) ANR-11-LBX-0044Agence Nationale de la Recherche (French National Research Agency) ANR-21-CE13-0047Agence Nationale de la Recherche (French National Research Agency) ANR-22-CE13-0009Fondation pour la Recherche Médicale (Foundation for Medical Research in France) FDM202106013570Grantová Agentura České Republiky (Grant Agency of the Czech Republic) GA23-04974SMinisterstvo Školství, Mládeže a Tělovýchovy (Ministry of Education, Youth and Sports) ERC CZ LL2323 FIBROFORCESchlumberger Foundation FSER20200211117Worldwide Cancer Research 24-0216
6 · The paper itself

Abstract

Fibroblasts are stromal cells found in connective tissue that are critical for organ development, tissue homeostasis and pathology. Single-cell transcriptomic analyses have revealed a high level of inter- and intra-organ heterogeneity of fibroblasts. However, the functional implications and lineage relations of different fibroblast subtypes remained unexplored, especially in the mammary gland. Here, we provide a comprehensive characterization of pubertal mouse mammary fibroblasts, through single-cell RNA sequencing, spatial mapping, functional assays, and in vivo lineage tracing. We unravel a transient niche-forming population of specialized contractile fibroblasts that exclusively localize around the tips of the growing mammary epithelium and are recruited from preadipocytes in the surrounding fat pad stroma. Using organoid-fibroblast co-cultures we reveal that different fibroblast populations can acquire contractile features when in direct contact with the epithelium, promoting organoid branching. The detailed in vivo characterization of these specialized cells and their lineage history provides insights into fibroblast heterogeneity and implicates their importance for creating a signalling niche during mouse mammary gland development.

Indexed as

FibroblastsMammary Glands, AnimalAdipocytesAnimalsCell LineageCoculture TechniquesEpithelial CellsEpitheliumFemaleMiceMice, Inbred C57BLOrganoidsSingle-Cell Analysis

Identifiers

PMID41022819
PMCPMC12480840

What OpenQuestion holds

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LicenceCC BY-NC-ND
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 OpenQuestion graph.