Thangaraju Muthusamy, Rudelius Martina, Bierie Brian, Raffeld Mark, Sharan Shikha, Hennighausen Lothar, Huang A-Mei, Sterneck Esta
Laboratory of Protein Dynamics and Signaling, Center for Cancer Research, National Cancer Institute, Frederick, MD 21702-1201, USA.
Development. 2005 Nov;132(21):4675-85. doi: 10.1242/dev.02050. Epub 2005 Sep 28.
The STAT3 transcription factor is an important initiator of mammary gland involution in the mouse. This work shows that the STAT3 target gene CCAAT/enhancer binding protein delta (C/EBPdelta) is a crucial mediator of pro-apoptotic gene expression events in mammary epithelial cells. In the absence of C/EBPdelta, involution is delayed, the pro-apoptotic genes encoding p53, BAK, IGFBP5 and SGP2/clusterin are not activated, while the anti-apoptotic genes coding for BFL1 and Cyclin D1 are not repressed. Consequently, p53 targets such as survivin, BRCA1, BRCA2 and BAX are not regulated appropriately and protease activation is delayed. Furthermore, expression of MMP3 and C/EBPdelta during the second phase of involution is perturbed in the absence of C/EBPdelta. In HC11 cells, C/EBPdelta alone is sufficient to induce IGFBP5 and SGP2. It also suppresses Cyclin D1 expression and cooperates with p53 to elicit apoptosis. This study places C/EBPdelta between STAT3 and several pro- and anti-apoptotic genes promoting the physiological cell death response in epithelial cells at the onset of mammary gland involution.
信号转导和转录激活因子3(STAT3)转录因子是小鼠乳腺退化的重要启动因子。这项研究表明,STAT3靶基因CCAAT/增强子结合蛋白δ(C/EBPδ)是乳腺上皮细胞中促凋亡基因表达事件的关键调节因子。在缺乏C/EBPδ的情况下,退化过程延迟,编码p53、BAK、胰岛素样生长因子结合蛋白5(IGFBP5)和SGP2/簇集蛋白的促凋亡基因未被激活,而编码BFL1和细胞周期蛋白D1的抗凋亡基因未被抑制。因此,诸如生存素、乳腺癌1号基因(BRCA1)、乳腺癌2号基因(BRCA2)和BAX等p53靶基因未得到适当调控,蛋白酶激活也被延迟。此外,在缺乏C/EBPδ的情况下,退化第二阶段的基质金属蛋白酶3(MMP3)和C/EBPδ的表达受到干扰。在HC11细胞中,单独的C/EBPδ足以诱导IGFBP5和SGP2。它还抑制细胞周期蛋白D1的表达,并与p53协同引发细胞凋亡。这项研究表明,在乳腺退化开始时,C/EBPδ处于STAT3与几个促凋亡和抗凋亡基因之间,促进上皮细胞的生理性细胞死亡反应。