Abstract
Progesterone-RankL paracrine signaling has been proposed as a driver of stem cell expansion in the mammary gland, and Elf5 is essential for the differentiation of mammary epithelial progenitor cells. We demonstrate that Elf5 expression is induced by progesterone and that Elf5 and progesterone cooperate to promote alveolar development. The progesterone receptor and Elf5 are expressed in a mutually exclusive pattern, and we identify RankL as the paracrine mediator of the effects of progesterone on Elf5 expression in CD61+ progenitor cells and their consequent differentiation. Blockade of RankL action prevented progesterone-induced side branching and the expansion of Elf5(+) mature luminal cells. These findings describe a mechanism by which steroid hormones can produce the expansion of steroid hormone receptor-negative mammary epithelial cells.
Publication types
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, Non-P.H.S.
MeSH terms
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Animals
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DNA-Binding Proteins / genetics*
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DNA-Binding Proteins / metabolism
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Epithelial Cells / drug effects
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Epithelial Cells / metabolism
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Epithelial Cells / physiology
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Female
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Gene Expression Regulation, Developmental / drug effects
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Gene Expression Regulation, Developmental / genetics
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Mammary Glands, Animal / drug effects*
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Mammary Glands, Animal / growth & development
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Mammary Glands, Animal / metabolism
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Mice
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Mice, Transgenic
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Progesterone / pharmacology*
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RANK Ligand / metabolism
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RANK Ligand / pharmacology*
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RANK Ligand / physiology
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Receptors, Progesterone / genetics
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Receptors, Progesterone / metabolism
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Receptors, Progesterone / physiology
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Stem Cells / metabolism*
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Stem Cells / physiology
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Transcription Factors / genetics*
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Transcription Factors / metabolism
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Up-Regulation / genetics
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Up-Regulation / physiology
Substances
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DNA-Binding Proteins
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Elf5 protein, mouse
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RANK Ligand
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Receptors, Progesterone
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Transcription Factors
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Progesterone