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Early lineage segregation of multipotent embryonic mammary gland progenitors

The mammary gland (MG) is composed of basal cells (BCs) and luminal cells (LCs). While it is generally believed that MG arises from embryonic multipotent progenitors (EMPs), it remains unclear when lineage restriction occurs and what are the mechanisms responsible for the switch from multipotency to...

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Detalles Bibliográficos
Autores principales: Wuidart, Aline, Sifrim, Alejandro, Fioramonti, Marco, Matsumura, Shigeru, Brisebarre, Audrey, Brown, Daniel, Centonze, Alessia, Dannau, Anne, Dubois, Christine, Van Keymeulen, Alexandra, Voet, Thierry, Blanpain, Cédric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5985933/
https://www.ncbi.nlm.nih.gov/pubmed/29784918
http://dx.doi.org/10.1038/s41556-018-0095-2
Descripción
Sumario:The mammary gland (MG) is composed of basal cells (BCs) and luminal cells (LCs). While it is generally believed that MG arises from embryonic multipotent progenitors (EMPs), it remains unclear when lineage restriction occurs and what are the mechanisms responsible for the switch from multipotency to unipotency during MG morphogenesis. Here, we performed multicolor lineage tracing and assessed the fate of single progenitors and demonstrated the existence of a developmental switch from multipotency to unipotency during embryonic MG development. Molecular profiling and single cell RNA-seq revealed that EMPs express a unique hybrid basal and luminal signature and the factors associated with the different lineages. Sustained p63 expression in EMPs promotes unipotent BC fate and was sufficient to reprogram adult LCs into BCs by promoting an intermediate hybrid multipotent like state. Altogether, this study identifies the timing and the mechanisms mediating the early lineage segregation of multipotent progenitors during MG development.