Targeting RANKL to a specific subset of murine mammary epithelial cells induces ordered branching morphogenesis and alveologenesis in the absence of progesterone receptor expression
| Autor: | Atish Mukherjee, Francesco J. DeMayo, Bin He, Yan Ying, John P. Lydon, Selma M. Soyal, Jie Li |
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| Rok vydání: | 2010 |
| Předmět: |
Cell type
Morphogenesis Estrogen receptor Mice Transgenic Biochemistry Research Communications Mice Mammary Glands Animal Pregnancy Progesterone receptor Genetics Animals Humans Progesterone Receptor Negative Receptor Molecular Biology Cell Proliferation Mice Knockout biology Gene Expression Profiling RANK Ligand Epithelial Cells Anti-Bacterial Agents Gene Expression Regulation Mammary Epithelium RANKL Doxycycline biology.protein Cancer research Female Receptors Progesterone Biotechnology |
| Zdroj: | The FASEB Journal. 24:4408-4419 |
| ISSN: | 1530-6860 0892-6638 |
| DOI: | 10.1096/fj.10-157982 |
| Popis: | Despite support for receptor of activated NF-κB ligand (RANKL) as a mediator of mammary progesterone action, the extent to which this cytokine can functionally contribute to established progesterone-induced mammary morphogenetic responses in the absence of other presumptive effectors is still unclear. To address this uncertainty, we developed an innovative bigenic system for the doxycycline-inducible expression of RANKL in the mammary epithelium of the progesterone receptor knockout (PRKO) mouse. In response to acute doxycycline exposure, RANKL is specifically expressed in the estrogen receptor α (ER) positive/progesterone receptor negative (ER+/PR−) cell type in the PRKO mammary epithelium, a cell type that is equivalent to the ER+/PR+ cell type in the wild-type (WT) mammary epithelium. Notably, the ER+/PR+ mammary cell normally expresses RANKL in the WT mammary epithelium during pregnancy. In this PRKO bigenic system, acute doxycycline-induced expression of RANKL results in ordered mammary ductal side branching and alveologenesis, morphological changes that normally occur in the parous WT mouse. This mammary epithelial expansion is accompanied by significant RANKL-induced luminal epithelial proliferation, which is driven, in part, by indirect induction of cyclin D1. Collectively, our findings support the conclusion that RANKL represents a critical mediator of mammary PR action and that restricted expression of this effector to the ER+/PR+ mammary cell-type is necessary for a spatially ordered morphogenetic response to progesterone.—Mukherjee, A., Soyal, S. M., Li, J., Ying, Y., He, B., DeMayo, F. J., Lydon, J. P. Targeting RANKL to a specific subset of murine mammary epithelial cells induces ordered branching morphogenesis and alveologenesis in the absence of progesterone receptor expression. |
| Databáze: | OpenAIRE |
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