Transcriptional landscapes underlying Notch-induced lineage conversion and plasticity of mammary basal cells

The mammary epithelium derives from multipotent mammary stem cells (MaSCs) that engage into differentiation during embryonic development. However, adult MaSCs maintain the ability to reactivate multipotency in non-physiological contexts. We previously reported that Notch1 activation in committed basal cells triggers a basal-to-luminal cell fate switch in the mouse mammary gland. Here, we report conservation of this mechanism and found that in addition to the mammary gland, constitutive Notch1 signaling induces a basal-to-luminal cell fate switch in adult cells of the lacrimal gland, the salivary gland, and the prostate. Since the lineage transition is progressive in time, we performed single-cell transcriptomic analysis on index-sorted mammary cells at different stages of lineage conversion, generating a temporal map of changes in cell identity. Combining single-cell analyses with organoid assays, we demonstrate that cell proliferation is indispensable for this lineage conversion. We also reveal the individual transcriptional landscapes underlying the cellular plasticity switching of committed mammary cells in vivo with spatial and temporal resolution. Given the roles of Notch signaling in cancer, these results may help to better understand the mechanisms that drive cellular transformation.

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Publication Details

Journal
The EMBO Journal
Published
2025-04-04
DOI
https://doi.org/10.1038/s44318-025-00424-1
Citations
2
Primary Topic
Cancer Cells and Metastasis
Type
article
Field-Weighted Citation Impact
2.09

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article

Transcriptional landscapes underlying Notch-induced lineage conversion and plasticity of mammary basal cells

Fabian Rost, Calvin Rodrigues, Candice Merle, Robin P. Journot et al.
2 citations
The EMBO Journal
Cancer Cells and Metastasis
2.09
article

Transcriptional landscapes underlying Notch-induced lineage conversion and plasticity of mammary basal cells

Fabian Rost, Calvin Rodrigues, Candice Merle, Robin P. Journot, Silvia Fré, Yiteng Dang, Steffen Rulands, Atefeh Pourkhalili Langeroudi
article en
2 citations

Abstract

The mammary epithelium derives from multipotent mammary stem cells (MaSCs) that engage into differentiation during embryonic development. However, adult MaSCs maintain the ability to reactivate multipotency in non-physiological contexts. We previously reported that Notch1 activation in committed basal cells triggers a basal-to-luminal cell fate switch in the mouse mammary gland. Here, we report conservation of this mechanism and found that in addition to the mammary gland, constitutive Notch1 signaling induces a basal-to-luminal cell fate switch in adult cells of the lacrimal gland, the salivary gland, and the prostate. Since the lineage transition is progressive in time, we performed single-cell transcriptomic analysis on index-sorted mammary cells at different stages of lineage conversion, generating a temporal map of changes in cell identity. Combining single-cell analyses with organoid assays, we demonstrate that cell proliferation is indispensable for this lineage conversion. We also reveal the individual transcriptional landscapes underlying the cellular plasticity switching of committed mammary cells in vivo with spatial and temporal resolution. Given the roles of Notch signaling in cancer, these results may help to better understand the mechanisms that drive cellular transformation.

The EMBO JournalVol. 44(10)
Centre National de la Recherche Scientifique (FR), Inserm (FR), Université Paris Sciences et Lettres (FR), Sorbonne Université (FR), Max Planck Institute for the Physics of Complex Systems (DE), Center for Systems Biology Dresden (DE), Max Planck Institute of Molecular Cell Biology and Genetics (DE), Génétique et biologie du développement (FR), Ludwig-Maximilians-Universität München (DE)
Worldwide Cancer Research, Agence Nationale de la Recherche, Fondation pour la Recherche Médicale, Fondation ARC pour la Recherche sur le Cancer, Université de Recherche Paris Sciences et Lettres, Fondation Schlumberger pour l’Education et la Recherche, HORIZON EUROPE European Research Council
Life in Land
Openalex Percentile: Top 13%
Cancer Cells and Metastasis
2.09
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