Nfatc1's Role in Mammary Epithelial Morphogenesis and Basal Stem/progenitor Cell Self-renewal

被引:2
|
作者
McNeil, Melissa [1 ]
Han, Yingying [1 ]
Sun, Peng [1 ]
Watanabe, Kazuhide [1 ]
Jiang, Jun [1 ]
Chen, Natasha [1 ]
Yu, Zhengquan [2 ]
Zhou, Bin [3 ,4 ,5 ]
Dai, Xing [1 ]
机构
[1] Univ Calif Irvine, Sch Med, Dept Biol Chem, Irvine, CA 92697 USA
[2] China Agr Univ, Coll Biol Sci, Dept Nutr & Hlth, State Key Labs Agrobiotechnol, Beijing 100193, Peoples R China
[3] Albert Einstein Coll Med, Inst Aging Res, Wilf Cardiovasc Res Inst, Dept Genet, Bronx, NY 10461 USA
[4] Albert Einstein Coll Med, Inst Aging Res, Wilf Cardiovasc Res Inst, Dept Pediat, Bronx, NY 10461 USA
[5] Albert Einstein Coll Med, Inst Aging Res, Wilf Cardiovasc Res Inst, Dept Med Cardiol, Bronx, NY 10461 USA
关键词
Mammary gland; Basal cell; Stem cell; Nfatc1; Self-renewal; STEM-CELLS; GLAND;
D O I
10.1007/s10911-021-09502-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Mammary gland is an outstanding system to study the regulatory mechanisms governing adult epithelial stem cell activity. Stem cells in the basal layer of the mammary gland fuel the morphogenesis and regeneration of a complex epithelial network during development and upon transplantation. The self-renewal of basal stem/progenitor cells is subjected to regulation by both cell-intrinsic and extrinsic mechanisms. Nfatc1 is a transcription factor that regulates breast tumorigenesis and metastasis, but its role in mammary epithelial development and stem cell function has not been investigated. Here we show that Nfatc1 is expressed in a small subset of mammary basal epithelial cells and its epithelial-specific deletion results in mild defects in side branching and basal-luminal cell balance. Moreover, Nfatc1-deficient basal cells exhibit reduced colony forming ability in vitro and somewhat compromised regenerative potential upon transplantation. Thus, our study provides evidence for a detectable yet non-essential role of Nfatc1 in mammary epithelial morphogenesis and basal stem/progenitor cell self-renewal.
引用
收藏
页码:357 / 365
页数:9
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