Zhao Dan, Ma Gui, Zhang Xiaolin, He Yuan, Li Mei, Han Xueying, Fu Liya, Dong Xue-Yuan, Nagy Tamas, Zhao Qiang, Fu Li, Dong Jin-Tang
From the Department of Genetics and Cell Biology, College of Life Sciences, Nankai University, Tianjin 300071, China.
the Ningbo Institute of Medical Sciences, Ningbo 315020, China.
J Biol Chem. 2016 Jun 10;291(24):12809-12820. doi: 10.1074/jbc.M116.719377. Epub 2016 Apr 20.
The zinc finger homeobox 3 (ZFHX3, also named ATBF1 for AT motif binding factor 1) is a transcription factor that suppresses prostatic carcinogenesis and induces neuronal differentiation. It also interacts with estrogen receptor α to inhibit cell proliferation and regulate pubertal mammary gland development in mice. In the present study, we examined whether and how Zfhx3 regulates lactogenic differentiation in mouse mammary glands. At different stages of mammary gland development, Zfhx3 protein was expressed at varying levels, with the highest level at lactation. In the HC11 mouse mammary epithelial cell line, an in vitro model of lactogenesis, knockdown of Zfhx3 attenuated prolactin-induced β-casein expression and morphological changes, indicators of lactogenic differentiation. In mouse mammary tissue, knock-out of Zfhx3 interrupted lactogenesis, resulting in underdeveloped glands with much smaller and fewer alveoli, reduced β-casein expression, accumulation of large cytoplasmic lipid droplets in luminal cells after parturition, and failure in lactation. Mechanistically, Zfhx3 maintained the expression of Prlr (prolactin receptor) and Prlr-Jak2-Stat5 signaling activity, whereas knockdown and knock-out of Zfhx3 in HC11 cells and mammary tissues, respectively, decreased Prlr expression, Stat5 phosphorylation, and the expression of Prlr-Jak2-Stat5 target genes. These findings indicate that Zfhx3 plays an essential role in proper lactogenic development in mammary glands, at least in part by maintaining Prlr expression and Prlr-Jak2-Stat5 signaling activity.
锌指同源盒3(ZFHX3,也称为AT基序结合因子1的ATBF1)是一种转录因子,可抑制前列腺癌发生并诱导神经元分化。它还与雌激素受体α相互作用,以抑制细胞增殖并调节小鼠青春期乳腺发育。在本研究中,我们研究了Zfhx3是否以及如何调节小鼠乳腺的泌乳分化。在乳腺发育的不同阶段,Zfhx3蛋白以不同水平表达,在泌乳期表达水平最高。在HC11小鼠乳腺上皮细胞系(一种泌乳生成的体外模型)中,敲低Zfhx3可减弱催乳素诱导的β-酪蛋白表达和形态变化,这些都是泌乳分化的指标。在小鼠乳腺组织中,敲除Zfhx3会中断泌乳生成,导致腺体发育不全,腺泡更小且数量更少,β-酪蛋白表达降低,产后管腔细胞中出现大量细胞质脂滴积聚,以及泌乳失败。从机制上讲,Zfhx3维持催乳素受体(Prlr)的表达以及Prlr-Jak2-Stat5信号活性,而分别在HC11细胞和乳腺组织中敲低和敲除Zfhx3会降低Prlr表达、Stat5磷酸化以及Prlr-Jak2-Stat5靶基因的表达。这些发现表明,Zfhx3在乳腺正常的泌乳发育中起重要作用,至少部分是通过维持Prlr表达和Prlr-Jak2-Stat5信号活性来实现的。