4.8 Article

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

Journal

CELL
Volume 127, Issue 5, Pages 1041-1055

Publisher

CELL PRESS
DOI: 10.1016/j.cell.2006.09.048

Keywords

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Funding

  1. NCI NIH HHS [R01 CA057621, R01 CA057621-16A1, R01 CA057621-15, CA057621] Funding Source: Medline
  2. NIEHS NIH HHS [ES012801, U01 ES012801, U01 ES012801-04S3] Funding Source: Medline

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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.

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