Evidence map›Paper›PMID 38760574›Full record

ArticleThe EMBO journal2024

Spatially distinct epithelial and mesenchymal cell subsets along progressive lineage restriction in the branching embryonic mammary gland.

Claudia Carabaña, Wenjie Sun, Camila Veludo Ramos, Mathilde Huyghe, Meghan Perkins, Aurélien Maillot, Robin Journot, Fatima Hartani, Marisa M Faraldo, Bethan Lloyd-Lewis and 1 more

Abstract read
In one paragraph

Article in The EMBO journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

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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

11 authors.

Claudia CarabañaInstitut Curie, Laboratory of Genetics and Developmental Biology, PSL Research University, INSERM U934, CNRS UMR3215, 75248, Paris, France.
Wenjie Sun *Institut Curie, Laboratory of Genetics and Developmental Biology, PSL Research University, INSERM U934, CNRS UMR3215, 75248, Paris, France.ORCID http://orcid.org/0000-0002-3100-2346
Camila Veludo Ramos *Institut Curie, Laboratory of Genetics and Developmental Biology, PSL Research University, INSERM U934, CNRS UMR3215, 75248, Paris, France.
Mathilde HuygheInstitut Curie, Laboratory of Genetics and Developmental Biology, PSL Research University, INSERM U934, CNRS UMR3215, 75248, Paris, France.ORCID http://orcid.org/0000-0002-8473-2924
Meghan PerkinsInstitut Curie, Laboratory of Genetics and Developmental Biology, PSL Research University, INSERM U934, CNRS UMR3215, 75248, Paris, France.ORCID http://orcid.org/0000-0002-7046-8747
Aurélien MaillotInstitut Curie, Laboratory of Genetics and Developmental Biology, PSL Research University, INSERM U934, CNRS UMR3215, 75248, Paris, France.ORCID http://orcid.org/0000-0001-9818-3287
Robin JournotInstitut Curie, Laboratory of Genetics and Developmental Biology, PSL Research University, INSERM U934, CNRS UMR3215, 75248, Paris, France.
Fatima HartaniInstitut Curie, Laboratory of Genetics and Developmental Biology, PSL Research University, INSERM U934, CNRS UMR3215, 75248, Paris, France.
Marisa M FaraldoInstitut Curie, Laboratory of Genetics and Developmental Biology, PSL Research University, INSERM U934, CNRS UMR3215, 75248, Paris, France.ORCID http://orcid.org/0000-0001-9497-1171
Bethan Lloyd-LewisSchool of Cellular and Molecular Medicine, University of Bristol, Biomedical Sciences Building, Bristol, BS8 1TD, UK. bethan.lloyd-lewis@bristol.ac.uk.ORCID http://orcid.org/0000-0001-6511-1818
Silvia FreInstitut Curie, Laboratory of Genetics and Developmental Biology, PSL Research University, INSERM U934, CNRS UMR3215, 75248, Paris, France. silvia.fre@curie.fr.ORCID http://orcid.org/0000-0002-7209-7636

Funding

Academy of Medical Sciences (The Academy of Medical Sciences) SBF003/1170Agence Nationale de la Recherche (ANR) ANR-10-INBS-04Agence Nationale de la Recherche (ANR) ANR-15-CE13-0013-01Agence Nationale de la Recherche (ANR) ANR-21-CE13-0047Agence Nationale de la Recherche (ANR) Labex Deep 11-LBX-0044EC | Horizon 2020 Framework Programme (H2020) 666003Fondation ARC pour la Recherche sur le Cancer (ARC) ARCPGA2021120004232_4874Fondation pour la Recherche Médicale (FRM) 12917Fondation pour la Recherche Médicale (FRM) EQU201903007821Fondation pour la Recherche Médicale (FRM) SPF202309017673Fondation Schlumberger pour l'Education et la Recherche (FSER) FSER20200211117Université de Recherche Paris Sciences et Lettres (PSL) C19-64-2019-228Wellcome TrustWellcome Trust (WT) 204813/Z/16/Z
6 · The paper itself

Abstract

How cells coordinate morphogenetic cues and fate specification during development remains a fundamental question in organogenesis. The mammary gland arises from multipotent stem cells (MaSCs), which are progressively replaced by unipotent progenitors by birth. However, the lack of specific markers for early fate specification has prevented the delineation of the features and spatial localization of MaSC-derived lineage-committed progenitors. Here, using single-cell RNA sequencing from E13.5 to birth, we produced an atlas of matched mouse mammary epithelium and mesenchyme and reconstructed the differentiation trajectories of MaSCs toward basal and luminal fate. We show that murine MaSCs exhibit lineage commitment just prior to the first sprouting events of mammary branching morphogenesis at E15.5. We identify early molecular markers for committed and multipotent MaSCs and define their spatial distribution within the developing tissue. Furthermore, we show that the mammary embryonic mesenchyme is composed of two spatially restricted cell populations, and that dermal mesenchyme-produced FGF10 is essential for embryonic mammary branching morphogenesis. Altogether, our data elucidate the spatiotemporal signals underlying lineage specification of multipotent MaSCs, and uncover the signals from mesenchymal cells that guide mammary branching morphogenesis.

Indexed as

Cell LineageEpithelial CellsMammary Glands, AnimalMesenchymal Stem CellsAnimalsCell DifferentiationFemaleFibroblast Growth Factor 10MesodermMiceMorphogenesisMultipotent Stem CellsSingle-Cell AnalysisFgf10 protein, mouseFibroblast Growth Factor 10Branching MorphogenesisEmbryonic ExplantsFate SpecificationMammary Stem CellsscRNA-seq

Identifiers

PMID38760574
PMCPMC11183262

What OpenQuestion holds

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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.