Notch3 marks clonogenic mammary luminal progenitor cells in vivo

被引:84
作者
Lafkas, Daniel [1 ,2 ,3 ,4 ]
Rodilla, Veronica [1 ,2 ,3 ]
Huyghe, Mathilde [1 ,2 ,3 ]
Mourao, Larissa [1 ,2 ,3 ]
Kiaris, Hippokratis [4 ]
Fre, Silvia [1 ,2 ,3 ]
机构
[1] Inst Curie, Ctr Rech, F-75248 Paris 05, France
[2] CNRS, UMR 3215, F-75248 Paris 05, France
[3] INSERM, U934, F-75248 Paris 05, France
[4] Univ Athens, Sch Med, Dept Biol Chem, GR-11527 Athens, Greece
关键词
GLAND DEVELOPMENT; SELF-RENEWAL; STEM-CELLS; KEY STAGES; COMMITMENT; BMI-1; DIFFERENTIATION; PROLIFERATION; MAINTENANCE; AMPLICON;
D O I
10.1083/jcb.201307046
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The identity of mammary stem and progenitor cells remains poorly understood, mainly as a result of the lack of robust markers. The Notch signaling pathway has been implicated in mammary gland development as well as in tumorigenesis in this tissue. Elevated expression of the Notch3 receptor has been correlated to the highly aggressive "triple negative" human breast cancer. However, the specific cells expressing this Notch paralogue in the mammary gland remain unknown. Using a conditionally inducible Notch3-CreERT2(SAT) transgenic mouse, we genetically marked Notch3-expressing cells throughout mammary gland development and followed their lineage in vivo. We demonstrate that Notch3 is expressed in a highly clonogenic and transiently quiescent luminal progenitor population that gives rise to a ductal lineage. These cells are capable of surviving multiple successive pregnancies, suggesting a capacity to self-renew. Our results also uncover a role for the Notch3 receptor in restricting the proliferation and consequent clonal expansion of these cells.
引用
收藏
页码:47 / 56
页数:10
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