TY - JOUR
T1 - Construction of developmental lineage relationships in the mouse mammary gland by single-cell RNA profiling
AU - Pal, Bhupinder
AU - Chen, Yunshun
AU - Vaillant, François
AU - Jamieson, Paul
AU - Gordon, Lavinia
AU - Rios, Anne C.
AU - Wilcox, Stephen
AU - Fu, Naiyang
AU - Liu, Kevin He
AU - Jackling, Felicity C.
AU - Davis, Melissa J.
AU - Lindeman, Geoffrey J.
AU - Smyth, Gordon K.
AU - Visvader, Jane E.
N1 - Publisher Copyright:
© 2017 The Author(s).
PY - 2017/12/1
Y1 - 2017/12/1
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85034642667&partnerID=8YFLogxK
U2 - 10.1038/s41467-017-01560-x
DO - 10.1038/s41467-017-01560-x
M3 - Article
C2 - 29158510
AN - SCOPUS:85034642667
SN - 2041-1723
VL - 8
JO - Nature Communications
JF - Nature Communications
IS - 1
M1 - 1627
ER -