R-spondin1 is a novel hormone mediator for mammary stem cell self-renewal

被引:85
作者
Cai, Cheguo [1 ]
Yu, Qing Cissy [1 ]
Jiang, Weimin [1 ]
Liu, Wei [1 ]
Song, Wenqian [1 ]
Yu, Hua [1 ]
Zhang, Lei [1 ]
Yang, Ying [1 ]
Zeng, Yi Arial [1 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Biol Sci, Inst Biochem & Cell Biol, State Key Lab Cell Biol, Shanghai 200031, Peoples R China
基金
中国国家自然科学基金;
关键词
mammary stem cell; niche; luminal cell; hormone; Rspo1; Wnt4; GLAND DEVELOPMENT; WNT/BETA-CATENIN; BETA-CATENIN; IN-VITRO; GENE-EXPRESSION; WNT PROTEINS; RECEPTOR; MOUSE; CANCER; GROWTH;
D O I
10.1101/gad.245142.114
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Signals from the niche play pivotal roles in regulating adult stem cell self-renewal. Previous studies indicated that the steroid hormones can expand mammary stem cells (MaSCs) in vivo. However, the facilitating local niche factors that directly contribute to the MaSC expansion remain unclear. Here we identify R-spondin1 (Rspo1) as a novel hormonal mediator in the mammary gland. Pregnancy and hormonal treatment up-regulate Rspo1 expression. Rspo1 cooperates with another hormonal mediator, Wnt4, to promote MaSC self-renewal through Wnt/beta-catenin signaling. Knockdown of Rspo1 and Wnt4 simultaneously abolishes the stem cell reconstitution ability. In culture, hormonal treatment that stimulates the expression of both Rspo1 and Wnt4 can completely substitute for exogenous Wnt proteins, potently expand MaSCs, and maintain their full development potential in transplantation. Our data unveil the intriguing concept that hormones induce a collaborative local niche environment for stem cells.
引用
收藏
页码:2205 / 2218
页数:14
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