Department of Surgery, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA.
Sci Transl Med. 2013 Dec 11;5(215):215le4. doi: 10.1126/scitranslmed.3006883.
In vivo menstrual cycle data support the findings by Tanos et al. that progesterone regulates RANKL in an ex vivo microstructure model of the human breast, but dispute the suppression of estradiol on progesterone-stimulated RANKL expression. RANKL responds to progesterone in a three-dimensional organoid culture model under conditions mimicking luteal-phase hormone concentration, suggesting that the microstructure may not be crucial to demonstrate progesterone responsiveness.
体内月经周期数据支持 Tanos 等人的研究结果,即孕激素在人乳腺的体外微结构模型中调节 RANKL,但孕激素刺激的 RANKL 表达不受雌激素抑制。在模拟黄体期激素浓度的三维类器官培养模型中,RANKL 对孕激素有反应,这表明微结构对于证明孕激素反应性可能不是至关重要的。