TY - JOUR
T1 - Dynamics of Lgr6+ progenitor cells in the hair follicle, sebaceous gland, and interfollicular epidermis
AU - Füllgrabe, Anja
AU - Joost, Simon
AU - Are, Alexandra
AU - Jacob, Tina
AU - Sivan, Unnikrishnan
AU - Haegebarth, Andrea
AU - Linnarsson, Sten
AU - Simons, Benjamin D.
AU - Clevers, Hans
AU - Toftgård, Rune
AU - Kasper, Maria
N1 - Publisher Copyright:
© 2015 The Authors.
PY - 2015/11/10
Y1 - 2015/11/10
N2 - The dynamics and interactions between stem cell pools in the hair follicle (HF), sebaceous gland (SG), and interfollicular epidermis (IFE) of murine skin are still poorly understood. In this study, we used multicolor lineage tracing to mark Lgr6-expressing basal cells in the HF isthmus, SG, and IFE. We show that these Lgr6+ cells constitute long-term self-renewing populations within each compartment in adult skin. Quantitative analysis of clonal dynamics revealed that the Lgr6+ progenitor cells compete neutrally in the IFE, isthmus, and SG, indicating population asymmetry as the underlying mode of tissue renewal. Transcriptional profiling of Lgr6+ and Lgr6- cells did not reveal a distinct Lgr6-associated gene expression signature, raising the question of whether Lgr6 expression requires extrinsic niche signals. Our results elucidate the interrelation and behavior of Lgr6+ populations in the IFE, HF, and SG and suggest population asymmetry as a common mechanism for homeostasis in several epithelial skin compartments.
AB - The dynamics and interactions between stem cell pools in the hair follicle (HF), sebaceous gland (SG), and interfollicular epidermis (IFE) of murine skin are still poorly understood. In this study, we used multicolor lineage tracing to mark Lgr6-expressing basal cells in the HF isthmus, SG, and IFE. We show that these Lgr6+ cells constitute long-term self-renewing populations within each compartment in adult skin. Quantitative analysis of clonal dynamics revealed that the Lgr6+ progenitor cells compete neutrally in the IFE, isthmus, and SG, indicating population asymmetry as the underlying mode of tissue renewal. Transcriptional profiling of Lgr6+ and Lgr6- cells did not reveal a distinct Lgr6-associated gene expression signature, raising the question of whether Lgr6 expression requires extrinsic niche signals. Our results elucidate the interrelation and behavior of Lgr6+ populations in the IFE, HF, and SG and suggest population asymmetry as a common mechanism for homeostasis in several epithelial skin compartments.
UR - http://www.scopus.com/inward/record.url?scp=84946737201&partnerID=8YFLogxK
U2 - 10.1016/j.stemcr.2015.09.013
DO - 10.1016/j.stemcr.2015.09.013
M3 - Article
C2 - 26607954
AN - SCOPUS:84946737201
SN - 2213-6711
VL - 5
SP - 843
EP - 855
JO - Stem Cell Reports
JF - Stem Cell Reports
IS - 5
ER -