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Estrogen modulates mesenchyme-epidermis interactions in the adult nipple
Wu, Hsing-Jung,Oh, Ji Won,Spandau, Dan F.,Tholpady, Sunil,Diaz III, Jesus,Schroeder, Laura J.,Offutt, Carlos D.,Glick, Adam B.,Plikus, Maksim V.,Koyama, Sachiko,Foley, John The Company of Biologists 2017 Development (Cambridge) Vol.144 No.8
<P>Maintenance of specialized epidermis requires signals from the underlying mesenchyme; however, the specific pathways involved remain to be identified. By recombining cells from the ventral skin of the K14-PTHrP transgenic mice [which overexpress parathyroid hormone-related protein (PTHrP) in their developing epidermis and mammary glands] with those from wild type, we show that transgenic stroma is sufficient to reprogram wild-type keratinocytes into nipple-like epidermis. To identify candidate nipple-specific signaling factors, we compared gene expression signatures of sorted Pdgfr alpha-positive ventral K14-PTHrP and wild-type fibroblasts, identifying differentially expressed transcripts that are involved in WNT, HGF, TGF beta, IGF, BMP, FGF and estrogen signaling. Considering that some of the growth factor pathways are targets for estrogen regulation, we examined the upstream role of this hormone in maintaining the nipple. Ablation of estrogen signaling through ovariectomy produced nipples with abnormally thin epidermis, and we identified TGF beta as a negatively regulated target of estrogen signaling. Estrogen treatment represses Tgf beta 1 at the transcript and protein levels in K14-PTHrP fibroblasts in vitro, while ovariectomy increases Tgfb1 levels in K14-PTHrP ventral skin. Moreover, ectopic delivery of Tgf beta 1 protein into nipple connective tissue reduced epidermal proliferation. Taken together, these results show that specialized nipple epidermis is maintained by estrogen-induced repression of TGF beta signaling in the local fibroblasts.</P>