Construction of developmental lineage relationships in the mouse mammary gland by single-cell RNA profiling

Bhupinder Pal(The University of Melbourne), Yunshun Chen(The University of Melbourne), François Vaillant(The University of Melbourne), Paul R. Jamieson(Walter and Eliza Hall Institute of Medical Research), Lavinia Gordon(Walter and Eliza Hall Institute of Medical Research), Anne C. Rios(The University of Melbourne), Stephen Wilcox(Walter and Eliza Hall Institute of Medical Research), Nai Yang Fu(The University of Melbourne), Kevin He Liu(Walter and Eliza Hall Institute of Medical Research), Felicity C. Jackling(Walter and Eliza Hall Institute of Medical Research), Melissa J. Davis(The University of Melbourne), Geoffrey J. Lindeman(The University of Melbourne), Gordon K. Smyth(The University of Melbourne), Jane E. Visvader(The University of Melbourne)
Nature Communications
November 14, 2017
Cited by 205Open Access
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Abstract

The mammary epithelium comprises two primary cellular lineages, but the degree of heterogeneity within these compartments and their lineage relationships during development remain an open question. Here we report single-cell RNA profiling of mouse mammary epithelial cells spanning four developmental stages in the post-natal gland. Notably, the epithelium undergoes a large-scale shift in gene expression from a relatively homogeneous basal-like program in pre-puberty to distinct lineage-restricted programs in puberty. Interrogation of single-cell transcriptomes reveals different levels of diversity within the luminal and basal compartments, and identifies an early progenitor subset marked by CD55. Moreover, we uncover a luminal transit population and a rare mixed-lineage cluster amongst basal cells in the adult mammary gland. Together these findings point to a developmental hierarchy in which a basal-like gene expression program prevails in the early post-natal gland prior to the specification of distinct lineage signatures, and the presence of cellular intermediates that may serve as transit or lineage-primed cells.


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