GATA-3 maintains the differentiation of the luminal cell fate in the mammary gland

被引:560
作者
Kouros-Mehr, Hosein
Slorach, Euan M.
Sternlicht, Mark D.
Werb, Zena
机构
[1] Univ Calif San Francisco, Dept Anat, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Program Biomed Sci, San Francisco, CA 94143 USA
关键词
ESTROGEN-RECEPTOR-ALPHA; BREAST-CANCER; REGULATORY NETWORKS; STEM-CELLS; GENE; EXPRESSION; PROLIFERATION; MORPHOGENESIS; REVEALS; IDENTIFICATION;
D O I
10.1016/j.cell.2006.09.048
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The GATA family of transcription factors plays fundamental roles in cell-fate specification. However, it is unclear if these genes are necessary for the maintenance of cellular differentiation after development. We identified GATA-3 as the most highly enriched transcription factor in the mammary epithelium of pubertal mice. GATA-3 was found in the luminal cells of mammary ducts and the body cells of terminal end buds (TEBs). Upon conditional deletion of GATA-3, mice exhibited severe defects in mammary development due to failure in TEB formation during puberty. After acute GATA-3 loss, adult mice exhibited undifferentiated luminal cell expansion with basement-membrane detachment, which led to caspase-mediated cell death in the long term. Further, FOXA1 was identified as a downstream target of GATA-3 in the mammary gland. This suggests that GATA-3 actively maintains luminal epithelial differentiation in the adult mammary gland, which raises important implications for the pathogenesis of breast cancer.
引用
收藏
页码:1041 / 1055
页数:15
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