Miyagawa Shinichi, Iguchi Taisen
Okazaki Institute for Integrative Bioscience, National Institute for Basic Biology, National Institutes of Natural Sciences, Okazaki, Aichi 444-8787, Japan; Department of Basic Biology, Faculty of Life Science, SOKENDAI (The Graduate University for Advanced Studies), Okazaki, Aichi 444-8787, Japan.
Okazaki Institute for Integrative Bioscience, National Institute for Basic Biology, National Institutes of Natural Sciences, Okazaki, Aichi 444-8787, Japan; Department of Basic Biology, Faculty of Life Science, SOKENDAI (The Graduate University for Advanced Studies), Okazaki, Aichi 444-8787, Japan
Proc Natl Acad Sci U S A. 2015 Oct 20;112(42):12986-91. doi: 10.1073/pnas.1513550112. Epub 2015 Oct 5.
Estrogen-mediated actions in female reproductive organs are tightly regulated, mainly through estrogen receptor 1 (ESR1). The mouse vaginal epithelium cyclically exhibits cell proliferation and differentiation in response to estrogen and provides a unique model for analyzing the homeostasis of stratified squamous epithelia. To address the role of ESR1-mediated tissue events during homeostasis, we analyzed mice with a vaginal epithelium-specific knockout of Esr1 driven by keratin 5-Cre (K5-Esr1KO). We show here that loss of epithelial ESR1 in the vagina resulted in aberrant epithelial cell proliferation in the suprabasal cell layers and led to failure of keratinized differentiation. Gene expression analysis showed that several known estrogen target genes, including erbB growth factor ligands, were not induced by estrogen in the K5-Esr1KO mouse vagina. Organ culture experiments revealed that the addition of erbB growth factor ligands, such as amphiregulin, could activate keratinized differentiation in the absence of epithelial ESR1. Thus, epithelial ESR1 integrates estrogen and growth factor signaling to mediate regulation of cell proliferation in squamous differentiation, and our results provide new insights into estrogen-mediated homeostasis in female reproductive organs.
雌激素在女性生殖器官中的作用受到严格调控,主要通过雌激素受体1(ESR1)来实现。小鼠阴道上皮会随着雌激素的作用周期性地出现细胞增殖和分化,为分析复层鳞状上皮的稳态提供了一个独特的模型。为了探究ESR1介导的组织事件在稳态过程中的作用,我们分析了由角蛋白5-Cre(K5-Esr1KO)驱动的阴道上皮特异性敲除Esr1的小鼠。我们在此表明,阴道上皮ESR1的缺失导致基底上层细胞层上皮细胞异常增殖,并导致角化分化失败。基因表达分析表明,包括erbB生长因子配体在内的几个已知雌激素靶基因,在K5-Esr1KO小鼠阴道中不会被雌激素诱导。器官培养实验表明,添加erbB生长因子配体,如双调蛋白,在没有上皮ESR1的情况下可以激活角化分化。因此,上皮ESR1整合雌激素和生长因子信号,以介导鳞状分化中细胞增殖的调控,我们的研究结果为雌激素介导的女性生殖器官稳态提供了新的见解。